Huberman Lab - Dr. Sara Gottfried: How to Optimize Female Hormone Health for Vitality & Longevity
Episode Date: January 30, 2023My guest is Sara Gottfried, M.D., a Harvard-trained, board-certified gynecologist and clinical assistant professor of integrative medicine & nutritional sciences at Thomas Jefferson University. Dr. ...Gottfried specializes in hormone health, vitality and longevity using precision/personalized approaches. We discuss female hormone health, puberty, perimenopause, and menopause, hormone testing, the microbiome, stress related hormone challenges, their causes, and various treatments. We also discuss fertility, birth control and tools for improving microbiome health, treating PCOS, insulin management, and the best nutrition, supplementation, and exercise programs for women. While the episode focuses mainly on female hormones, males will also  benefit from our discussion because it includes  actionable tools suggested for managing stress, bolstering the gut microbiome, and immunity—all of which stand to improve overall health, vitality and longevity in males and females. For the full show notes, visit hubermanlab.com. Thank you to our sponsors AG1: https://athleticgreens.com/huberman LMNT: https://drinklmnt.com/huberman Supplements from Momentous https://www.livemomentous.com/huberman Timestamps (00:00:00) Dr. Sara Gottfried (00:04:07) Sponsor: LMNT (00:07:50) Women, Family History, Heredity & Environment (00:11:00) Puberty, Stress, Menstrual Cycles, Intrauterine Devices (IUDs) (00:17:26) Tool: Sex Hormones, Microbiome, Estrobolome & Disease; Biomarker Testing (00:25:11) Nutritional Testing; Vegetables, Microbiome & Disease (00:27:33) Sponsor: AG1 (00:32:22) Microbiome, Prebiotics & Probiotics, Inflammation (00:36:08) Microbiome Testing, Magnesium, Constipation & Thyroid (00:42:25) Female Colonoscopy; Network Effect & Modern Medicine, Stress Factors (00:45:13) Constipation, Stress & Trauma, Autonomic Balance (00:55:35) Constipation Relief, Stress, Breathwork & Meditation (01:02:58) Systemic & Societal Stress Unique to Females (01:09:23) Testing & Future Behavior (01:11:55) Polycystic Ovary Syndrome (PCOS) & Cardiometabolic Disease; Stress (01:22:57) PCOS, Insulin, Glucose Monitoring and Management; Data Access (01:29:48) Behaviors for Vitality; Exercise & Body Phenotype; Cortisol (01:36:40) Cortisol Supplements: Ashwagandha, Rhodiola, Fish Oil, Phosphatidylserine (01:42:36) Cortisol, Anxiety & Immune System; Adrenal Function, Resilience (01:48:07) Tool: Omega-3 Fatty Acids, Inflammation, Specialized Pro-Resolving Mediators (01:54:20) Oral Contraceptives, Benefits & Risks; Ovarian Cancer; Testosterone (02:06:50) Fertility, Follicular & Anti-Mullerian Hormone (AMH) Assessments (02:10:29) Menopause & Hormone Replacement Therapy; Women’s Health Initiative (02:15:30) Perimenopause, Cerebral Hypometabolism, Metabolism & Estrogen (02:21:49) Intermittent Fasting, Ketogenic Diet, Metabolic Flexibility (02:23:29) Stool Testing (02:25:32) Coronary Artery Calcium (CAC) Test, ACE Score & Disease (02:31:56) Zero-Cost Support, YouTube Feedback, Spotify & Apple Reviews, Sponsors, Social Media, Neural Network Newsletter, Momentous Title Card Photo Credit: Mike Blabac Disclaimer
Transcript
Discussion (0)
Welcome to the Huberman Lab podcast where we discuss science and science-based tools for everyday life.
I'm Andrew Huberman and I'm a professor of neurobiology and
Ophthalmology at Stanford School of Medicine. Today my guest is Dr. Sarah Gottfried. Dr. Sarah Gottfried is an obstetrician
gynecologist who did her undergraduate training in bioengineering at the University of Washington in Seattle.
who did her undergraduate training in bioengineering at the University of Washington in Seattle. She then completed her medical training at Harvard Medical School,
and she currently is a clinical professor of integrative medicine and nutritional sciences
at Thomas Jefferson University. She has also been a clinician,
treating men and women in various aspects of hormone health and longevity for more than 20 years.
She is an expert in not just traditional medicine
as it relates to hormones and fertility,
but also nutritional practices,
supplementation and behavioral practices,
and combining all of that expertise
in order to help women navigate
every aspect and dimension of their hormones,
longevity and vitality,
ranging from puberty to young adulthood,
adulthood, perimenopause, and menopause.
And nowadays, she's also treating men
across the lifespan in terms of longevity,
vitality, and hormone health.
During today's discussion, Dr. Gottfried shares
an enormous amount of information and tools
that women can apply toward their hormone health,
fertility, vitality, and longevity.
We discuss the gut microbiome, which many people have heard about, but Dr. Gottfried points
out the specific needs that women have in terms of managing their gut microbiome and the ways
that that influences things like estrogen levels and metabolism, testosterone thyroid,
and growth hormone, and much more.
We also discuss nutrition and exercise.
We touch on how the omega-3 fatty acids play a particularly important role in managing
female hormone health. We touch on how the omega-3 fatty acids play a particularly important role in managing female
hormone health. Dr. Gottfried points out why women have particular needs when it comes to
essential fatty acids and how best to obtain those essential fatty acids for hormone health.
We also discuss exercise and she offers some surprising information about the types and ratios
of resistance training to cardiovascular training that women ought to use in order to maximize
their hormone health. We also talk a lot about the digestive system. This was a surprising aspect
of the conversation I did not anticipate. Dr. Gottfried shared with us for instance that women suffer
from digestive issues at more than 10 times the frequency that do men. And fortunately that there
are tools specific to women that they can use in order to overcome those digestive issues and that in overcoming those digestive issues, they can overcome many of the related
hormone issues that so many women face.
Dr. Gottfried also shares with you tremendous knowledge about the specific types of tests,
not just blood tests, but also urine and microbiome tests that women can use in order to really
get a clear understanding of their hormone status, not just of present,
but also where the trajectory of their hormones is taking them.
So we have an avid discussion about puberty, about young adulthood, adulthood, perimenopause,
and how best to manage and navigate perimenopause and menopause, including a discussion about hormone
replacement therapy.
In addition to our academic and clinical expertise,
Dr. Gottfried has authored many important books on nutrition,
hormones, and supplementation as it relates to women
and to people generally.
The two books that I'd like to highlight and that we provided links to
in the show note captions are women, food, and hormones, and the hormone cure.
I read the hormone cure and found it to be tremendously interesting and informative,
not just in terms of teaching me about female hormone health and various treatments for female hormone
health, but also as a man trying to understand how the endocrine system interacts with mindset,
nutrition, and supplementation more generally.
So I highly recommend the hormone cure for anybody interested in hormones and hormone health,
and women food and hormones in particular for women, although again, in both books are going to be strongly informative for women wishing to optimize their hormone health, and women food and hormones in particular for women, although again, in both books, are going to be strongly informative for women wishing to optimize their hormone
health, vitality, and longevity.
Before we begin, I'd like to emphasize that this podcast is separate from my teaching
and research roles at Stanford.
It is, however, part of my desire and effort to bring zero cost to consumer information
about science and science-related tools to the general public.
In keeping with that theme,
I'd like to thank the sponsors of today's podcast.
Our first sponsor is Element.
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Again, that's DrinkElementLMNT.com slash Huberman.
And now for my discussion with Dr. Sarah Gottfried.
Dr. Gottfried, Sarah, welcome.
Thank you.
So happy to be here.
Yeah, I'm delighted and very excited to ask you
about an enormous number of topics.
You are an expert in so many things.
So the challenge for me is going to be
to constrain this walk that we're,
but I'm hoping that we can touch on
a great number of things today.
The first of which is really about hormones
and female hormones in particular.
And I have a question which is,
is it ever informative for a woman regardless of age
to know something about her mother's,
perhaps even her grandmother's experience
vis-a-vis hormones, not just pregnancy challenges with
or ease with pregnancy and child rearing childbirth
this sort of thing, but you know what sorts of conversations should women be having with
themselves and with family members to get a window into what their specific needs might be.
Love this question. So my work is really at the interface between genetics and environment.
So your question gets to both.
And I think it's essential that you understand what your grandmother went through.
I'd even say your great-grandmother, depending on longevity in your family.
So I grew up with my great-grandmother, I get that.
And especially your mother. So I would probably start first with
trauma and intergenerational trauma because I think that affects the endocrine system so hugely,
especially cortisol signaling, but the broader pine system, psychoimmune neuroendocrine system.
psychomino neuroendocrine system. And then there's, you know, if I think about the stages,
the life cycle that a woman goes through,
if you think about puberty, I think,
I don't know how genetically determined the age of puberty
is certainly there's a lot of environmental influences
like toxins can affect it.
But pregnancy, the age at which you start to go through
parimenopause, menopause, many of those have a genetic component. So with pregnancy, I mean,
you can certainly think the shape of the pelvis, your ability to have a vaginal birth,
some of that is genetically determined. I mean, you do have the sperm donor affecting some of that.
But in my family, for instance, we have no cesarean sections.
So everyone goes through this process
of a relatively easy vaginal birth.
I was a four-steps baby, but for the most part,
you can find out about that.
And then there's certain female conditions that have a very strong component,
genetically, most of which run in my family. So that includes endometriosis,
fibroids. I just had an asterectomy. I had a 50-plus fibroates and polycystic ovarian syndrome.
And of those three, how frequent are those?
And maybe I can constrain the question a little bit by saying, today's discussion I imagine
is going to be heard by men and women of all sorts of ages.
So I, maybe I'll direct the question a little bit toward, you know, at what age should
these discussions start?
You know, we always imagine that women in their 30s and 40s and 50s and onward should be getting certain tests
and addressing things like ovarian reserve
and other sorts of things.
But, you know, maybe we could march through
and just say, for a woman in her teens
who's already hip puberty, what sorts of biomarkers,
whether or not they're blood based or phenotyping,
the outward appearance of,
should those young women be paying attention to,
likewise for women in their 20s, 30s,
maybe we could take it more or less by decade,
starting at puberty,
assuming that woman hits puberty,
sometime what between
what is it now? The average in the US is somewhere between 12 and 16 years old. Do I have that
right?
No, you do not.
Oh, great.
So that is...
So it used to be 12 to 16. I would say 50 years ago. It's been moving younger. And we
think some of that is related to toxin exposure,
as I mentioned, but I was 10 when I went through puberty.
So I should say men are key,
and I started growing breasts much before that.
So I think now I'm going to step away from the science
for a moment.
I'm going to do that pretty fluidly,
and I'll try to call it out.
I think there's also a huge influence from stress and like the development of the adrenal glands.
So going back to the science, the issue in teenage years is that the hypothalamic pituitary
adrenal axis, and I like to think of it broader.
So stay with me.
Hypothelamic pituitary adrenal,
good natal, over recent women, testes men, thyroid, gut axis.
So that means the control system.
So I'm kind of expressing my bioengineering side here.
Well, I think it's great to include the other organs
and tissue systems of the body,
because as we both know,
that the narrow definition of just hypothalamic pituitary adrenal,
it can't be just that, right?
No.
It can't, right?
No.
It doesn't tell the whole story.
So if you look at the main sex hormones in a young woman who's in her teenage years, the hypothalamic pituitary
adrenal-good-nattle part of that is not fully mature.
So they're more likely to skip periods, especially under stress.
They have a lot of influences that really doesn't get well-established until you're
done with adolescents.
And I'm told that adolescents now is till like age 25 to 26. I heard that and I was like, I've got
two daughters. I was like, that's a really long time.
Not just psychologically defined or biosec...
So mostly, mostly psychologically defined. I heard that from a psychologist. So,
biomarkers you asked about.
In your teenage years, what I think is really interesting
is to look at cortisol.
To look at the dance between estrogen and progesterone
in those years is less helpful, because I
think there's a lot of variability due to the immaturity
of the system.
If you've got someone who's got really regular periods,
it's probably better to do some benchmarking at that age,
but generally, I find that benchmarking
is best performed in your 20s or 30s.
Are periods not that regular in terms of duration
of the menstrual cycle when the menstrual cycle first sets in?
It depends.
So I was like clockwork every 28 days
until I had my hysterectomy in August.
Same thing with my daughters.
I've got two daughters, one, 17, the others, 23.
For a lot of women, they're not regular.
And then there's the whole piece of oral contraceptives
and other forms of contraception
where you have no idea what the
normal cycle is. And I hope we'll have some time to talk a little bit about oral contraceptives because
I think it is, this is now a opinion again in that science. I think it is the number one endocrinopathy
that is eye-adrogenic for women. We will definitely talk about it. I get a lot of questions about oral contraceptives
in the social media space and also questions about IUDs
quite a lot.
In particular, copper IUDs, non-hormonal IUDs.
So we will definitely touch on that.
I'm an IUD crusader, so I just wanna give you that warning.
You're a fan, do I have that right?
Or you're anti-IUD. I am a huge fan. Uh-huh. Which IUDs in particular? So I like copper because it's non-hormonal
It's as effective as getting your tubes tied. Who would have thought right? I mean, it's that toxic to the sperm mobility
Is that how it works? That's my understanding of it is that that it that it basically it's like a and it
More or less an electric fence to the sperm cap and that's it.
Electric fence is a bit of a harsh analogy, but I'll work with that.
But it's, you know, to have something that can last for 10 years so that you really
have complete autonomy and sovereignty over your sexual life, that's profound. And to not get all
those downstream brists, there is a seed with birth control pill. The other thing that's
important to know about it, I know this is a cypher. Women who use the copyrighted have
the highest satisfaction rate of anyone on contraceptives, The highest satisfaction rate. And yet, it is the least used of all forms of contraception.
Now, my favorite is vasectomy.
But, short of vasectomy, I think that idea is a really great choice.
There are some risks associated with it.
I'm not saying it's risk-free, but I love that idea.
And I love it for younger women, too, because it used to be that
when I went through my training, which was
30 years ago, we were told, you know, don't put it in someone who hasn't had a baby and
That is patriarchal messaging, but getting back to your original question, which is about biomarkers per decade
In your 20s
That's when you want to do some base casing with estrogen and progesterone
and testosterone.
So, I think it's really helpful to know about this tango.
You're from Argentina or your father's.
I have a Argentine lineage.
My grandparents did tango into their late 80s.
I am in my late 40s and I still haven't started. So I suppose there's time.
It might be time for you to. Okay. And it might be a factor in their longevity.
Did they have good health span? Not just health span. And my grandfather smoked cigarettes daily,
remained mentally sharp until he died in his late 90s, but almost burned down their apartment
several times, falling asleep with a cigarette in his mouth.
So I don't recommend anyone spoke, by the way,
but it was coffee, mate, red meat, and cigarettes
and they lived into their 90s.
So that side of my family has the genetic advantage,
the other side, less so, but in any event,
Tango is a 2023 goal, it has been every year.
I'm gonna hold you accountable to that. We'll do. And there know there will be no YouTube video of me doing.
At least not initially. Tim Ferris, actually, phenomenal podcaster, as we know is,
he's a badass tango dancer. I know this through various sources.
Yes. I've seen. Yeah. So this tango between estrogen and progesterone is incredibly important.
You want to have the right lead,
you want to have the right follow between the two hormones.
Again, I'm stepping away from my science app.
But what happens a lot of the time
is that estrogen dominates in that tango.
And when that happens, it sets you up
for greater risk of fibroids and ametriosis,
breast pain, probably in association with the microbiome and the astrobulum.
Can you familiarize me with the astrobulum?
Yeah.
I'm delighted to know that I don't recognize the term.
Yeah.
So the astrobulum is the set of microbes in and their DNA, their DNA mostly in the gut microbiome that set of microbes in their DNA.
So it's in the, if you look at the totality, the subset of particular bacteria modulate estrogen levels. So a lot of this work was spirited by Martin
Glaser and what we know is that there are some women who have an astrub alone
that makes them have a greater risk of certain estrogen-mediated
conditions like breast cancer, endometrial cancer, and a men prostate cancer.
So the astral form is incredibly important.
There's not a lot of attention paid to it,
but I always think in terms of my patients,
you know, could this be someone who's got a faulty astral form,
and we need to adjust it with, you know with some of the microbiome modulating nutrients,
nutraceuticals that we have so that they're less likely to have that tango
that's not working with estrogen and potassium.
So getting back to the biomarkers, if you gave me an unlimited budget,
which I kind of have with some of my clients
that I work with now,
what I would want to know is estrogen,
progesterone, testosterone,
and I want the timing right for that.
I'd want to know about DHEA
and sort of the whole androgen pathway.
I'd want to know about the metabolites of estrogen
because some of them are protective and very helpful.
Others are a bit like Homer Simpson. I mean, they're just like costing all kinds of problems in your
body, increasing the risk of quinones, like DNA damage, and potentially an increased risk of
breast cancer, although that data I think is mixed.
I'd also like to know about their stool,
so I wanna know about the microbiome.
So the best that we have right now is to look
when we do stool testing, I do a lot of stool testing.
We can look at things like beta, glucoronidase,
are you familiar with BG?
I'm familiar with it as a term,
and so for those listening, very often, not always,
when you hear an ACE, ASE, you're dealing with an enzyme.
So we can take a stab there.
And it sounds like it's somehow involved
in glucose metabolism of some sort.
Or is it glucuronidation?
So it's involved in, when you produce estrogen in the body,
this is like the simplified version,
but when you produce estrogen,
you are meant to use it,
like send it to the receptors where it's meant to go,
and then lose it.
Like you don't wanna keep recirculating estrogen
like bad karma,
and that's what happens with people who have high
beta glucoronides.
So it's this enzyme that's produced by three bacteria in particular in the gut.
And I see a lot of men and women who have elevated beta glucuronidase, and then they have
semester shendominants related to that.
Is that the total reason we don't really know?
But it's one of the drivers, it's one of the lovers.
And it can be detected from a microbiome,
AK stool sample.
That's right.
And in terms of blood testing, or various tests
for these other biomarkers, getting estrogen,
testosterone, and other ratios, I realize there are,
people have different means, financial means,
but in general, people wanting to do a blood test,
it sounds like they're going to need to do it.
What women will need to do it at different stages of their menstrual cycle.
If they had to pick one, either in the follicular phase or in the luteal stage of their ovarian
menstrual cycle, excuse me, ovulatory menstrual cycle, when would you suggest they do that?
If they had to pick one.
So, if you forced me to pick one, I would say probably day 21 to 22 for someone in
her 20s. So we're focused right now on that decade. So for most women, they've
got a menstrual cycle date that averages out at 28 days. So this is about a week
before they start their period. For women or more irregular, it's harder to do
that. As women get older and we'll
talk about this in a moment, usually the cycle gets a little shorter. So as they start
to decline in their progesterone production, their period gets a little closer together.
Like mine before August was about every 26 days. So at that point, you want to test sooner
like day 19, 20.
And I'm not talking about blood tests.
Blood tests is the cheapest thing.
It's usually what's covered by insurance.
But my preference would be to do dried urine.
I like to use saliva for cortisol.
I like to use dried urine so that I get metabolomics in addition to the levels of these hormones.
And if I'm forced to, I'll use blood testing.
And that's certainly the gold standard for all of these hormones. And if I'm forced to, I'll use blood testing. And that's certainly
the gold standard for all of these hormones that we're talking about. But it's not as comprehensive.
And as you know, it's a quick little snapshot while the needles in your vein for, you know, 30 seconds.
Yeah, the salivary cortisol makes sense to me because my understanding is that you get free
cortisol, which is the active cortisol. You said, with urine, you're also getting them a tabolites.
That's right.
And then for blood testing, you're getting sort of a crude window into the averages.
A static, total level.
So let me go back and say one other thing about biomarkers.
A big part of the testing that I do in phenotyping my patients, I practice precision
medicine, so I like to almost start with nutritional testing. I don't think I've ever had a teenager.
I've got some NBA players that are 19, 20, 21, so maybe those count, but those are men, obviously.
maybe those count, but those are men, obviously. But for nutritional testing, that would be potentially
a helpful thing to do in your 20s.
Becomes less important as you get older
and you develop more micronutrient deficiencies.
But micronutrients play a huge role
in terms of hormone production, magnesium.
You know, the magnesium is hugely involved
in the way that you get rid of estrogen. That's an example.
So micronutrient testing, what I usually do is a combination of blood and urine.
And so I'm looking at all of the micronutrients that we can measure that have some clinical
scientific basis behind them. If I could do that for a teenager, I think it might be helpful because I recently gave
a lecture on breast cancer risk reduction, another quick sidebar.
And I was sad to find that intake of vegetables, polyphenols is such an important predictor,
a future risk of breast cancer like
when you're at 50, 60 plus, and the most important time is when you're a teenager.
Now I have one daughter that eats vegetables, she loves them, and I have another
daughter who eats food that's beige, and it's very hard to get her to eat the
volume of vegetables, you know, five colors a day, which is what I do. And if you
have evidence that you could show a 17 year old that they've got micronutrient gaps, I
think that would be a motivator for them to eat differently. At a time when it's so critical,
even though it's, you know, 25 years in the future that it's going to potentially
change this arc that they're on. What do you do for a young woman who doesn't like vegetables,
or is it not somehow able or willing to get those five colors a day of vegetable to help support
the microbiome? Are supplements a useful tool in that case? What other sorts of tools
behavioral or otherwise are useful? Such a good question. So here I'm going to invoke Rob Knight
at UCSD. So I think his got project has really been helpful in terms of understanding what kind
of modulators are gonna be important.
So what I try to get that person to do,
and I don't see many teens anymore,
other than MBA players,
what I try to get them to do is have a smoothie.
Very hard to get them to have a smoothie every day,
but if I could get them to have a smoothie three times a week
and throw some of these vegetables in,
that makes a huge difference.
I mean, we know that makes a difference in terms of microbiome change.
She should be blending up broccoli or kale.
Call flowers.
So call flowers, even they're putting things into the smoothie.
Yeah, I don't know if you can get a teenager to do that, but they often will use,
like I have them do steam broccoli that's in the freezer because it's got very
little taste.
So that they could do that in a chocolate smoothie.
They could add some greens.
I like greens, powders are super convenient.
So that with kind of a taste that they like,
whether that's chocolate, which is what most of my clients want,
or vanilla with berries and that sort of thing.
So that can go a long way if you don't like vegetables.
And short of that, I would say some supplements,
but I would say that's a distant second
to making a smoothie.
I've got one patient that I have to mention
because he took this to the extreme.
So he's a retired physicist professor at UCSD.
He found out that his microbiome was a hot mass and developed autoimmune disease.
And so he became hellbent, like only a physicist could on changing his microbiome and he dramatically
shifted it by having a smoothie every day with 57 vegetables and fruits in it.
57 independent. 57 independent.
57 independent.
So I mean, this just warms my heart the way that he did this, but he would go to the
farmer's market, he would just get a bunch of this, a bunch of that, and he would go home
make the smoothie, and then stick it in the freezer, so he'd have a serving every day. And he became a completely different person based on this microbiome change.
His autoimmune disease is in remission.
He dropped a huge amount of weight.
He went from being kind of this phenotype that I know you know well of a professor high performing traveling around the world on so many boards
So much innovation so many great ideas super computer guy to be in someone who gets up in the morning gets in his hot tub
Exercises for like one to two hours a day and then does a little work
Like he completely shifted the way that he lives.
And his microbiome shift, who knows what's the chicken
and what's the egg there?
But he had a huge change in his physiology.
Glucose went from being quite high.
He had, and he tracks all of this, of course.
It's like on a Jupiter.
Science is after all.
Right.
And retired, I suppose might have had a lot of work.
And he's retired.
But he's got the longest time series of anyone I know.
And he's tracked his glucose and insulin going back 20 years. So he can show you, okay, here's where I started having my smoothie.
And here's how my glucose and insulin change. That's the result of that. I'd like to take a quick break and acknowledge one of our sponsors, Athletic Greens. Athletic
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Is there a case for, I'll say young women, but young women and men using over the counter
probiotics as a way to enhance the microbiome.
This is something I hear about a lot.
I've heard that excessive doses of capsule probiotics
can give a brain fog-like condition.
I personally don't use capsule probiotics
unless I feel like my system is under a significant amount
of stress in which case I might add that in
for brief periods of time,
or if I've just taken antibiotics for a period of time.
Do you ever recommend that the college student or the high school student that she or he
take capsule probiotics, assuming that they're getting, let's say, three to five servings
of vegetables per day, either in smoothie form or some other form?
What are your thoughts on supplementing probiotics?
It sounds like such a simple question.
It is such a complex answer.
And I don't think we really have the answer.
So I'll tell you the way that I approach it.
I look for randomized trials to support my use of probiotics.
And frankly, I'm underwhelmed.
So I've seen some data.
If I invoke my MBA players for a moment. Almost every player I've tested has
increased intestinal permeability. They just have such a high training load, probably
mediated by cortisol, very high glucose is when they drain, that they have increased intestinal
permeability. So those tight junctions in their intestine become loose. They develop a lot
of inflammation as a result of that.
And when you're a professional MBA player
and you're making 20 million a year,
like you don't want a lot of inflammation,
you want a little bit to help your muscles recover,
but you don't want it to be adding to problems
when you develop an injury.
So this is leaky gut.
This is actually, yeah.
I don't love that term, but yeah, we'll use it here.
So there's a particular probiotic that is helpful in athletes with leaky gut.
So that's the kind of specificity and randomized trial that I'm looking for.
The rest of it, I think there's support if you find help from it.
As you described, if you take a course of antibiotics, I mean, first of all, I would question
whether you need them.
But I try to avoid them.
There have been instances where they've been prescribed and I took them.
Mostly in the past, I go to college, they seem like they gave them out.
You had a science infection to give you antibiotics, using kind of like-
Yeah, the worst treatment ever.
Yeah, so if you're coming off of antibiotics, I think that's a good time to do what we call
replacement dose probiotics.
I think what's far more interesting is prebiotics.
I think the data is much better for prebiotics and a selective use of polyphenols.
Would a person in their teens and 20s or any age for that matter know
what whether or not they have nutritional deficiencies? What is the best way to analyze if one is
getting enough magnesium? And for that matter, what is going to be the best way to test the
microbiome? You said stool sample and I'll come right back with the same question I asked about blood test. What time of day, when during the month, to establish a baseline?
So this would be prior to embarking on 97 vegetables or how it works per day.
I love the idea that you're telling us, if I'm gathering correctly, is that yes, there's
a case for probiotics, but for the typical person regardless of age, eating more vegetables or drinking more vegetables as the case may
be, is going to be beneficial for the gut microbiome.
Perhaps without the need to go test whether or not one is making a certain number of estrogen-related
metabolites or not, just that's a great starting place, eat or consume more vegetables.
But if one wants to analyze their gut microbiome, are there good tests available to the general public?
This has been, I'm not gonna name companies,
but I've been tracking this over the years,
and it's never been clear to me that we know
what constituents of the gut microbiome are best.
You know, we know that dysbiosis is bad,
and we know that diversity of the microbiome is good.
We hear this, but no one's ever told me
that you want a particular ratio of one microbiota to another
in a way that has made any sense to me at least.
Totally.
I'm not a microbiologist, but whereas with testosterone and men, we hear, okay, you want
your free testosterone to be about 2% of your total perhaps with women.
Women are going to have more testosterone than estrogen on average, but still less than men
when you look at testosterone, et cetera, et cetera.
But you can get some crude measures.
But for the microbiome, it just seems like
long lists of microbiota for which I just get dizzy.
I just, if you just rode out a bunch of eyes and Ls
and Ss, you can kind of halfway.
You get a bit the same information.
I'm not trying to poke at that field, it's a beautiful field,
but they haven't told me what my microbiota ought to look like.
Like what's a healthy microbiome chart?
Well, that's because we don't know.
I mean, the best we have is Rob Knight's work,
but even that is limited in terms of, you know,
can I tell you that a woman in her 20s
should have this particular pattern with her microbiome? No, I can't.
So, let me go to your first question because I think you just asked about six.
Your first question is about nutritional testing.
What I like to do with nutritional testing is run a panel that's looking at antioxidants, so like vitamin A, vitamin C,
alpha-lipoic acid, plant-based antioxidants,
because you can measure that in the blood.
I like to look at some of the key vitamins,
especially the B-vitamin range,
because as you probably know,
if you've got particular genetic polymorphism,
you might be less likely to be absorbing the right level
of vitamin B9, full aid, vitamin B12, etc.
I'm also looking going back to the antioxidants
at glutathione because I think that's such an important
lever when it comes to detoxification,
which we haven't talked about yet.
And then I'm looking at some of the minerals.
Magnesium is really the most important
and we know that somewhere around 70 to 80 percent of Americans are deficient
in magnesium. That's like the lowest hanging fruit.
I would be curious, for instance, like with magnesium, if that number of people are deficient,
does that mean that that number of people should be targeting their nutrition towards foods
that contain magnesium and or supplementing with magnesium. And if so, what forms of magnesium?
We've talked about mag 3 and 8. Firstly, there's a maccitrate. There's so many forms.
It can be a little bit overwhelming to people. So any detail and sourcing would appreciate it.
Great. So first, in terms of testing, what I prefer to do is to mention one more than one lab
and more than one brand.
And I can just, I'm speaking mostly from experience. So for testing, I do a lot of Genova Neutra valves.
During the pandemic, they developed an ad home test.
Normally with a Neutra valve, you have to get your blood drawn
and you have to do a urine sample.
So a lot of people can't do that.
The great thing about this test is your insurance
usually pays for most of it.
And so the copay is about $150.
So during the pandemic, they developed another test
called Metabolomics, which does much of the same testing,
but it's a finger prick.
So most of my patients prefer that.
And in fact, they haven't gone back to the Neutrival.
Second lab is Spectrosol.
I use Spectrosol occasionally.
I find it not quite as easy in terms of fitting into my practice, but I've got friends and
mentors like Mark Houston who does a lot of precision cardiometabolic health. He thinksrosol is the best test out there.
So you asked about magnesium.
You have to measure red blood cell magnesium, like whole blood.
And with deficiency, it's interesting with supplementation.
For my patients who tend toward constipation, and that's frankly about 80% of the women that I take care of.
Really?
Yes.
Wow.
I'd be curious as to why that is.
I can guess, diet, stress.
Patriarchy, rage.
Psycho, psychosis.
They may not know about it.
So the pine system. The pine system.
Right.
Psychology, immunology, neural and endocrine factors combined.
Is that...
Yes.
And then I would say there's another factor, which is being female is a health hazard.
So we've twice the rate of depression, insomnia.
We've got 3 to 4x increased risk of multiple sclerosis.
We've got 5 to 8 times the risk of thyroid dysfunction.
So if you just look at that and you look at subtle preclinical thyroid dysfunction,
a huge number of the women that I take care of,
well let me pop off, a large number of the women that I take care of, well let me pop off, a large number of the women that I take care of, have thyroid dysfunction
that's contributing to constipation. And if we go back to that control system,
hypothermic pitudary adrenal thyroid canadal, gut access, and they have a lot of
perceived stress together with this borderline thyroid function that no
mainstream medicine doctor has told her is a problem. And then she's got a problem A lot of perceived stress, together with this borderline thyroid function that no mainstream
medicine doctor has told her is a problem, and then she's got a problem with the tango
between estrogen and progesterone.
She's going to tend toward constipation.
Women have a lot more constipation than men.
The gut is about 10 feet longer in women compared to men.
We should talk about some sex and gender differences and define
those. And they are much more likely to have a torturous colon. And the way you know
that is you get a colonoscopy and they tell you, yeah, it's really hard to get in there
and do what we need to do. As a brief tangent, but I think this is the
time to ask, what age now do physicians insist their female patients
get colonoscopies?
For men, I think the age used to be 50.
Now it's getting ratcheted back to 45 or 40.
Again, these are recommendations, not requirements, but they're pretty strong recommendations from
depending on where you live, et cetera.
For women, how early do you think they should get a colonoscopy to explore for possible
polyps end or colon cancer?
Yeah, it's a really good question.
I don't know the answer.
So what I've always operated with is 50.
The way that I answer that is to go to the US Preventive Task Force rating to determine
based on their synthesis of the data, what age is the most appropriate?
Has it changed? You just described from men from 50 to younger?
I don't know, so we should back to that.
All these additional health hazards for women, you mentioned some of the broadly mentioned
psychological impact, right?
And of course, these things are all related, psychology, immunology.
And one of the, I think wonderful things about neuroscience and science in general and medicine
is that there's now and, and understanding that all the organs are connected to one another.
It's a network. It's a network. And that the microbiome sits at, at, at a key node within
that network. And I think most people accept that now. Yeah. That seems to be a theme that at
least in the last 10 years is really wonderful because certainly for neuroscience, it was
thought that, you know, unless it's in the cranial vault, it's not neural, which is ridiculous
because there's lots of nervous system outside the skull. But in any case, for a second,
yes, please. So I think you're right that there's an understanding about the network effect, but I
think that as much as I love mainstream medicine and I trained in it and I am so grateful for
my education, I still think it is a silo-based way of taking care of patients.
So, even if there's an understanding of the network effect more at the science level
or as you described in neuroscience,
there's still, you know, if you are a woman
who has constipation fatigue,
maybe an autoimmune condition,
feel stressed out all the time,
feel like your hormones are out of whack,
you get sent to the gastroenterologist for the constipation, you get sent to the rheumatologist
for your autoimmune issues, you maybe get sent to an endocrinologist if you've got thyroid problems,
and there's very little collaboration between these groups. So even though there's an understanding
of the network of fact in real life, it's not happening.
Let's go deeper down that path because you point out something really important
and you've mentioned constipation a few times.
Can we view constipation as a serious enough symptom
that it warrants an immediate intervention?
That is, does it flag or signal problems
that are severe enough that that should be the issue
that's dealt with
for anybody that's experiencing it. I mean, it's sort of an odd topic for many people because they
think, oh, you know, bowel movements and sort of, you know, there's that kind of pre-adolescent
humor around this. But I think it's so important. What I'm hearing you say is that constipation
is far more common in women and it signals a general set of many problems occurring.
Does that mean that women should address constipation?
And if so, what's the best way to address constipation?
Yeah, I love this question because you're doing,
can we have a quick little meta conversation?
So you're doing something that I knew you would do,
which is you're teaching me something
and you're changing, like there's a social genomics thing happening
where you're changing my thought about this.
So I just wanted to acknowledge that thing.
Thank you.
Well, I think for me, when I hear that there's a kind of,
you know, you're talking about a phenotype,
constipation is a phenotype.
It's one that people generally don't wear a t-shirt
explaining it to people,
but that I'm guessing anything to do with sexual health,
bowel health, urology, people just don't
talk about.
For all sorts of reasons.
And those reasons are probably so obvious that they're not even worth discussing.
And also because we won't change them, except by talking about them.
So if you say women are far more constipated and that signalling a larger set of problems. Yes. Then my immediate thought is, well, we're leaving constipation
pun intended retroactively.
Will that assist in a great number of issues?
And or will it get them down the road of thinking about those other issues more specifically?
Like, do I need more magnesium or should I be putting vegetables in my smoothie?
You know, so I'm curious about constipation as a target for intervention that then opens up a bunch of
other discussions because there are these certain nodes in the mental health physical health space
that when someone, we talk a lot of deliberate cold exposure. Do I think it's magic? No, but I think
that if someone's getting themselves into a cold shower once a day, it opens up a number of questions about themselves and reveals a number of things to themselves.
Like, how do I offer stress? What sorts of levels of control do I actually have? And on and on. So perhaps not the best example.
But some of us hate cold exposure. Right. We have, we have like a gene that makes us stress out like you wouldn't believe, which I would argue makes it very likely that even
10 seconds of cold exposure gets you the effect that you want.
As opposed to someone who adores cold exposure like a penguin, needs a lot more cold exposure
for it to have the adaptive response.
Anyway, that's my way of gumbying through that quite, you're quite correct.
So let's answer this question.
It's a constipation issue. Yeah. So this is how you're changing the way I think about this.
So you're asking, okay, instead of looking at
constipation as a constellation of symptoms,
what about if you just used it on its own as sort of a key indicator or signal of
dysfunction with my network or maybe something broader.
And I think that's right.
So it makes me think of a few things.
It makes me, you're also changing this book that I'm writing on autoimmunity and trauma.
So thank you for that.
So women experience more trauma than men.
This is well established.
If you look at the ACE studies that were done
by the CDC and Kaiser in 1998,
we know that men for the most part, middle-aged men,
have about 50% of them experience significant trauma
as defined by the ACE questionnaire.
Women are at 60%.
And that's pretty durable since 1998. So women
have more, they have different forms of abuse, much more likely to have sexual abuse. They
have a different HPA response than men. Their perceived stress tends to be higher and I'm
generalizing for a population. Site note, you know, in precision medicine, we don't do that.
We do medicine for the individual, not the population, not medicine for the average.
And so if you look at the physiology of a female, I think that constipation and that need
to like control and restrain and hold things in, you know, tighten the
anal sphincter.
I think that's part of the physiology.
So I'm veering away from the science, but I do think that it is a really important signal
to pay a lot of attention to.
Now you also asked about microbiome testing.
Should we do that or do you?
Yeah, well I have a couple more questions about constipation.
I never thought I'd ask this many questions about constipation, but now I'm fascinated.
By the way, also this morning, I taught medical students at Stanford about the fact that
we are basically a series of tubes.
So you talked about the anal sphincter.
We are a set of swinkters from one end to the other.
We are a set of tubes.
I had a nervous system being one of those tubes.
And I think in Eastern medicine, they talk about the various locks between those tubes
and chambers.
And it's not without coincidence. There's some real wisdom there, of course. Wait, did you just talk about
energetic anatomy? More or less, I didn't say the word chakras, but I might in passing.
That's the bond does that. The bond us right are the, are the, the, the, the sphincters, right?
Yes. That's right. Thank you for that. The, so what defines constipation? I mean, in other words, let's think about the healthy, rather than think about the unhealthy,
let's how many bowel movements should a woman or a man have per day, assuming this is where
it gets tricky because some people are doing time restricted feeding, some people are eating
more, some people eating more fiber, more bulk, larger meal at the end of the day, a larger
meal at the beginning of the day, we will never be able to sort out all those variables, but on average, how many bowel movements
and is timing during the day for bowel movements at all informative?
What works for you?
Well, when I'm asleep, generally, I don't want a bowel movement.
So I'm going to be like most people, right?
Well, sleep is primary for you.
Right, exactly. I'm I always assumed that morning time. Yeah, was a was a healthy time for bowel movements. And
I think almost everybody babies included
Recognize the feeling of being lighter and more energetic when they've evacuated totally totally totally in fact so much
So that I'm obsessed with
Jungian and Freudian psychology,
the first thing we learn when we come into this world
is that we want something we feel
some sort of autonomic arousal stress,
whether or not it's food or warmth,
or the need to have a bowel movement.
One of the first things that parents learn
is how to recognize that,
not by the odor coming from the diaper,
but by the look on the baby's face
or their agitation.
Agitation signals the need for some sort of relief,
temperature relief, food relief, evacuating the bowel relief.
So my understanding is that as autonomic arousal increases
in the early part of the day, ideally,
after a good night's sleep, that bowel movements
become more likely, unless that arousal becomes so great that then people feel, so quote unquote, locked up.
Right. Because of the balance of the autonomic features. So early day, I'm
guessing, and again in the second half of the day, and here I'm totally guessing,
and certainly not having to wake in the middle of the night. Yeah, those are my
best guesses. That's great. So I would agree with that.
When I was at Harvard Medical School in UCSF residency, I was taught that constipation
is having a bowel movement less frequently than one every three days.
So I don't think I've ever laughed out loud on this podcast as the consequence of a textbook
medical knowledge.
Are you kidding me?
Is that ridiculous?
Well, that sounds like, and here pun intended,
that sounds like the conclusion of some very
conservative, emotionally,
and in other ways constipated individuals.
And again, this might seem like an odd conversation,
but the discussion around conservation
is present in psychological literature because of this
relationship to the autonomic system.
Well, it's a metaphor in literature.
It's crucial.
So you spoke to a number of different threads that I think are important here.
So that's the definition that I learned.
And I heard that and I was like, hell no, that doesn't work for me.
It doesn't work for anyone I know. And I spent a lot of time, especially in medical school
and in my internship where you rotate on medicine,
disimpacting women, like older women who come in,
who have an adabound movement in a month.
Whoa.
And that, let me tell you, that is not nice for anybody.
Yeah, believe me, I became a scientist
and I have a physician for a number of reasons.
That's one of them.
Both positive and negative, that's one of them.
Yeah.
So my definition of constipation as a Western mostly white girl
is that if you're not having a bowel movement every single
morning and you have a feeling of complete evacuation. Anything less than that is
constipation. So that's how I define it. If you're in India and you're eating food that's got a
fair amount of microbes in it, it's less, you know, sanitary, musing outward, as carefully as I can.
using that word, as carefully as I can. Generally, they have a bowel movement after every meal.
But they've got a different microbiome.
They're exposed to different microbes.
Here in the US, I would say once a day,
you also spoke to something very important,
which is the balance between the parasympathetic nervous
system, rest and digest and poop, versus the sympathetic nervous system,
kind of the on button, you know, fight, flight, freeze, on.
So I think for those of us who've got issues
with autonomic balance, it can lead to constipation.
And I like that constipation could be pulled out and kind of writ larger as an important signal.
What sorts of tools do you recommend people use to relieve constipation?
Eating more fiber, sounds like reducing stress is going to be a huge one.
Yes.
What are your favorite stress reduction tools?
I like to divide these into real-time tools.
So we have a big proponent of physiological sign, real-time, you know, these sorts of things.
But things that can really lower the baseline on stress overall to facilitate constipation
and other broad indicators of health.
So I'm not a fan of lowering stress.
I'm a fan of lowering perceived stress.
And I think the distinction is really important.
I learned when I was in my 30s
that I was a massive stress case and I didn't know it.
It was a sort of, I think I, through residency,
through working under 20 hours a week,
I just was so accustomed and sort of...
That was 120.
In 20, not under 20, folks.
Yeah, not unusual in medicine.
Well, they've changed training so that you work
no more than 80 hours a week now,
but that was before my time.
So I became accustomed to a massive amount of cortisol, massive.
And I would say I've spent the past 20 years really working on perceived stress
to find, I think all of us need an all-acart menu of what is most effective.
So what works for me now at my age is different than, you know, the TMI did as a college student,
transcendental meditation. It's different than the I became a certified yoga teacher when I was in
my 30s. That is very effective for a lot of people. It wasn't enough for my matrix.
I do a wholeotropic breath work.
I didn't read it, but I saw that she just had a paper and sell on your sign.
And it made me think, like, teach me how to sigh.
Teach me how to sigh.
Like, can you say a little bit about that?
Like, can you do it?
Yeah, very briefly that study was we wanted to find a minimal effective dose intervention. Yeah, five minutes.
I just want it. Yeah, so five minutes a day. We need to figure out what people do every day. Yeah, and we were monitoring
subjective mood, et cetera, but also biometrics remotely. So it's kind of a nice study. Which biometrics? HIV?
HIV
Night time sleep. Portisol?
I wish.
So this was done during the pandemic.
More than 100 subjects.
The advantage was that we got data 24 hours a day,
because they're pinging us in their data.
We're in the 20-24.
Yeah.
Nice.
So that was nice.
Resting heart rate, subjective mood,
we would get in touch with them daily.
So when people were swapped between groups
like any good study, but five minutes a day of sort of
standard, if you will, forgive me, meditations,
or just sitting, no instructions about how to breathe,
just focusing on, closing their eyes and focusing on focusing.
Yep.
Another group did box breathing,
inhale, hold, exhale, hold for equal durations.
The duration of each of those,
inhales and holds was set by their carbon dioxide tolerance. So somewhere
between three and eight seconds depending on how well they regulate
carbon dioxide. Another group did cyclic signs, so this would be double
inhale through the nose. So big inhale through the nose, followed by it to lungs empty exhale.
That second inhale, after the first big lung inhale through the nose is really important
because it makes sure that all the collapsed avioli lungs snap open and then the exhale
you offload a lot of carbon dioxide.
That's very similar to holotropic breath work.
Not yes, not unlike holotropic breath work,
little bit pranayama-ish,
but the exhale is rather passive, as opposed to active.
And then the fourth category was cyclic hyperventilation,
which is a lot like tummo, aka whim-hoff-ish breathing,
different than whim-hoff breathing.
So this would be, so very active inhales and exhales.
Every 25 cycles of inhale exhale,
that would be one cycle, long exhale, hold lungs empty,
15 to 30 seconds, then repeat for about five minutes.
Everyone did that for five minutes.
And what we found was that the cyclic sighing
led to the greatest improvements in mood around the clock,
not just around the practice or during the practice,
as well as lowered resting heart rate, improvements in sleep around the clock, not just around the practice or during the practice, as well as lowered resting heart rate,
improvements in sleep, et cetera.
And you got to publish and sell.
So amazing.
Very fortunate.
I think thankfully the reviewers and editors
understood that these minimal intervention things,
hopefully, are going to be of use to people.
So useful to people.
I mean, how often do you read a paper like that?
That could offer a behavior change
That is so easy to implement. I mean, I love that question. Thank you
So what about did you tell them not to drink because alcohol is such a huge effect on HIV?
Yeah, so in this case, we didn't tell them to alter anything else about their behavior
Just hoping it was background kind of effect on HIV. Yeah. So in this case, we didn't tell them to alter anything else about their behavior.
Just hoping it was background kind of across the sand.
That's true.
All great.
Yes. And some were Stanford students.
Others were from the general population.
Any of the fat boys that were drinking heavily?
Probably not.
Well, during the pandemic, I think alcohol intake went way up across the board.
I mean, it's enough.
I had a magic wand.
I would I would ask that people either not drink or drink two drinks per week maximum. At least that's my understanding of the board. I mean, it's enough. I had a magic wand. I would, I would ask that people either not drink or drink two drinks per week maximum. At least that's my understanding
of the literature. Are you familiar with the Woop data with alcohol? No, but we have a
collaboration with through that paper. Yeah. And it certainly disrupts patterns of nighttime
sleep in particular, my understanding that first phase of sleep that's related to the
massive growth hormone release that you all really need and want in their first-
And you did measure growth hormone?
We did not.
No.
The second iteration of this study will certainly include free cord is all by saliva, hormone
panels.
Well, I'm beginning to think that we should also be asking people how often they're going
to the bathroom and what time of day.
Yes.
I mean, this thing around constipation is super interesting.
And I think that plus blood markers,
and then I'm very excited to learn that urine contains
additional markers that could be informative.
So yeah, it was a fun study, not easy study
to do with that number of subjects.
Tastes a lot of draining for your research assistance.
Yeah, it was a big group.
It was nine people in our group and three clinicians
and a lot of phone calls and a lot of back and forth.
But, you know, and thank you to the subjects
who served as the real life guinea pigs.
So, yeah, I think that stress, you know, people's,
I think people are starting to appreciate
that there are ways that they can relieve their stress
that don't all only fall under the categories of vacation
and meditation, but I want to say that meditation is
obviously a wonderful tool. It's just it's a tool, not unlike any other tool that is great for
some people, unless great for others. Well, certainly it's a great tool and it's got such a scientific
basis behind it. But there's so many things on this ol' cart menu, sacs, ordasm, connection, feeling heard and seen and loved.
Yeah, let's talk about that.
You know, you mentioned earlier
that all these stress factors, you said patriarchy, right?
But I think what if I may, at risk of just strengthening
that, statement, I mean, that to me
is signaling a bunch of other factors around as you said, keeping
things in.
What do you think explains, let's talk about that, because I think that that's likely to
have raised a certain flag in people's minds.
Like, what exactly is she talking about?
Are you talking about less opportunity?
Are you talking about less opportunity to vocalize? Are you talking about less opportunity to vocalize?
Are you talking about less opportunity to vocalize and be heard?
I mean, I realize that there are an infinite number of variables,
but given that it sounds like a really strong input to the system,
what I mean by that is that psychology is influencing biology,
and you're saying that these power dynamics structures and dynamics
are impacting.
Let's hear your thoughts on that because I hate to let a flag like that go by without
fleshing it out.
Never waste a good flag.
Well, and let's preface it by just saying that people will have different opinions on
this and I think that's healthy and like with the discussion about constipation, let's
talk about what people aren't willing to talk about when it comes to health.
Love it. So we might need to talk about patriarchy on part two, but I'll give you some material that
I've been working with. I started, I did not even understand the existence of patriarchy until I was
a bioengineering undergraduate. At MIT, I should mention, which has always had a bit of a male,
a skewed male in terms of faculty numbers.
Well, that's true at most universities.
True. Well, my post-doc advisor was the late Ben Barris,
who was a female to male transition, transgender,
first transgender member of the National Academy of Sciences,
were my closest friends, unfortunately,
he died of pancreatic cancer.
We were very, very close.
They're actually making a documentary about Ben.
But Ben, this is interesting, Ben went to MIT
because he wanted to be around a lot of men.
Yeah.
That's a lesser known fact.
But then he was a very strong advocate for women.
He went to As Barbara when he was Barbara.
And by the way, he's given me permission to share all this.
Prior to his death, I recorded a lot of conversations.
I've been.
I only ever knew him as Ben, by the way.
But when he was at MIT, he was identified female.
And he later talked about the intense suppression,
oppression,
literally is how he described it,
especially given that he was performing so well.
Yes, so you just defined patriarchy.
You did it yourself.
Couple things.
When I was in bioengineering,
I took a women's studies class
and it was all about teaching undergraduates about the existence
of patriarchy, which I would define maybe at its simplest as power over.
I'm not saying men are patriarchy.
I'm saying something very different, which is power over.
Let me correct one thing that she said, I didn't go to MIT as an undergraduate.
So I was in Alaska and I went to the University of Washington for bioengineering.
In Seattle.
In Seattle.
I dropped out of a graduate program in bioengineering to go to the Harvard MIT program for health
sciences and technology in Boston.
Thanks for that clarification. University of Washington also wonderful place.
I have many, many, many, many wonderful close colleagues there. It's an incredible place,
especially for vision science.
It's especially good for engineering, bioengineering.
But, yeah, so my, my MD is jointly between MIT and Harvard and it's the oldest
maybe largest although Harvard says it was a lot program for biomedical engineers and
MD PhDs position to scientist training program
Great thanks for that clarification. I'm gonna blame the internet for this
I am I think we need to send our Wikipedia editors out. I think LinkedIn is correct.
Okay. Great. Well, Wikipedia editors note, get out there and make the correction. Now you heard it.
So stress that what you're really talking about is systemic stress in the body as a consequence of an environment.
That's right.
But there's particular forms of it.
I would say this also relates to white privilege.
It relates to racism.
And when you look at the way that systems, including my beloved MIT, the way that they're set up is that might make makes right.
And generally the people that are the strongest, you know, big men, strong men, they're the ones who tend to be the most successful.
So for people who are bi-pocked, for people who don't have white white privilege for women, it's a different experience.
And so I'm using patriarchy as kind of a umbrella here,
but it connects to many other things.
I wanna use this as an opportunity to a,
keep this in mind as we turn to a question
that I didn't close the hatch on earlier,
and it's my fault, which is,
I'm now clear on
the fact that a woman in her late teens early 20s ought to know something about her testosterone
estrogen thyroid cortisol levels should start at least thinking about her microbiome, should
be thinking about how many bowel movements and the timing of those bowel movements per
day, really. How many bowel movements in the timing of those bowel movements per day? Really and
I'm assuming that what I just described is also true for women in their
20s 30s 40s 50s on up to hundreds. Is that correct?
That's correct, but I would say that there are
differential opportunities by decade
so I'm glad she circled it back to teenagers and
testosterone because I think if you know, for instance, in your teenage years that you
have high endrogens and that you've got this potential phenotype way into the future that
you may not even notice. I mean, maybe you know that you've got a few extra hairs on your
chin or something. If you know that your testosterone is elevated or some
other endogen, it might change the arc of how you take care of yourself. So I think that
could be very helpful in your teenage years. In your 20s, for people who are a stress case
like me, so age 27 on the words at UCSF, if I had known that I was such a high cortisol
person, I think I would have done things differently. I would have changed my behavior.
And I don't know because I didn't base case these, but your testosterone can decline starting
your 20s, kind of depending on how much stress your matrix is under.
So for women that can start as early as 28.
Usually your testosterone declines by about 1% per year.
What level of testosterone do you like to see in a woman once she's sort of post, let's say after age 25,
what kind of range is healthy? I know what the reference range is only because I know one could look it up.
I don't know if the top of my head. But what's a kind of a nice reference point
there?
The way I tend to describe this on podcasts is the top half of the normal range.
Great. That I think is a good benchmark. For PCOS, generally, it's much higher than that. You know, I've seen patients
with PCOS where there are total testosterone. It's 100 to 200.
Do they always have peripheral manifestations of that? A little bit of hair, the skin
plaques. I've heard about, you know, so darkened skin plaques.
Regular periods. Regular periods is that, you know, I get a lot of questions about PCOS.
Yeah. And you're the first person we've had on this podcast.
It's really qualified to talk about PCOS in a real way.
So here we're talking about too many antigens,
cis-somni-ovary, irregular ovarian men's, excuse me,
I keep saying that, ovulatory slash menstrual cycle.
What are some other indicators?
And do you recommend that women start taking
undergen blockers or I mean how do it seems to be a lot of PCOS out there I'm hearing about it a lot.
So glad you asked about this.
So PCOS is one of those really poorly understood conditions that gets,
it kind of flows, flies below the radar until a woman wants to get pregnant
or she's got some other issue that drives her to a physician. The problem is that it is a syndrome,
right? So polycystic ovary syndrome, sometimes polycystic ovarian syndrome, and syndromes don't
necessarily fit together into a really clear diagnostic criteria.
So in this instance, there are three different criteria that we look for.
So this is some of the ovaries having clinical manifestations of hyperandrogenism, so that
could be horsytism, acne, other things, and then usually irregular periods. And the way that that's defined, at least by the latest
criteria, is having a period every 35 days or less.
So typical cycle length 28 days, 35 days,
you're skipping a period here and there.
So those are the criteria that we use to diagnose PCOS.
There are about four different systems out there in the literature for diagn diagnose PCOS, there are about four different systems out there
in the literature for diagnosing PCOS, which is where it starts to get confusing. So there's
some women who have no cysts on their ovaries, but they've got heretism and they've got
irregular periods. Could you define heretism? Heretism is increased hair growth, usually
in places that you don't want it. So for women, it can be kind of male pattern.
They might notice it on their breasts, on their chest.
And then there's, of course, a familial quality to that.
Like I was just looking at a paper last night looking at Israelis and how much here
satism they have.
And whether this is related to C.A. CHG repeats on the antigen receptor.
Do they get not Israelis, but do women who might have PCOS experience antigenic alopecia?
So hair loss that sort of of the quote unquote male pattern baldness.
Of course, it's antigen pattern baldness as opposed to male testosterone, DHT related.
Sometimes, you know, this is where I'm gonna invoke
clinical experience rather than what I've seen
in the literature.
Women definitely can have some antigenic alopecia.
I tend to see it later in life.
But this is an important point because we think of PCOS
as, you know, I was just talking about it in teenage years,
like wouldn't it be nice to know that you have this phenotype in your risk for all the things that people are at
risk for?
And we haven't talked about glucose and insulin yet, we should.
What we know is that PCOS is not just a problem in terms of irregular periods and then difficulty
getting pregnant.
So those are mostly problems in your 20s, 30s, early 40s, but it is a
massive risk factor for cardiovascular disease as you could older. So many
people tend to pitch in whole PCOS as a problem of reproductive age. We have to
be thinking of it over the entire female life cycle. And I would say it's even
more important to consider it over the age of 50, you know,
average age of menopause is 51 to 52, because we know that that elevated testosterone, the high
androgens, are probably the greatest cardiopulè´¸ with a driver of disease for women with PCS.
Now one other thing I want to mention, and I still have my notes that we're going to talk about
microbiome testing because that's such a fun subject.
What I was taught to do, again, saying this was so much love
for the people who have taught me how to do medicine.
What I was taught to do is that if you have a woman with PCOS,
you make the diagnosis, you measure or test oscarone,
you see if she has acne, blah, blah, blah.
You ask that woman one question.
Do you want to get pregnant or not?
So then you have these women with PCOS who get started on a birth control pill if they
don't want to get pregnant.
If they want to get pregnant, then you help them get pregnant by addressing some of these
PCOS issues like maybe you give them clom by addressing some of these PCOS issues, like
maybe you give them Clomid or you do something to make them ovulate more frequently.
That is the way that most conventional medicine approaches this, and it does women at gigantic
disservice.
One of the things I'm speaking into is the gender gap that exists.
My feeling is that the research money that goes into women's health is abysmal compared to what goes into men's health.
Really?
And I think that's changing, but there's also a huge lack of awareness of sex and gender differences when it comes to the way that we construct clinical trials and other experiments.
Well, that's absolutely true. I mean, I sit on, I've sat on an age review panels for more than a decade now
I'm a regular standing member, which is only to say that I see the research as it's being proposed. Yes. And now
It's required no grant will get funded without
Sex as a biological variable. And here I'm by the way folks this is sex
Biological sex the noun not sex the, both are super interesting, obviously.
But when we say sex is a biological variable,
meaning even if it's a study on mice,
we have to-
Where did that start though?
That didn't start that long ago.
It must have been, I think we can thank,
I don't want to misattribute you here.
I think we can thank Francis Collins
for insisting on this.
Amen, Francis.
And Bernadine Healy has done so much to help us,
but you know, she made the Women's
Health Initiative, which I hope will get you, which is a hot mass, like so confusing the
data that came out of that.
But-
Yeah.
But-
And these trials are long, and so the data are only now starting to emerge, so just to be
clear.
I mean, I have a question that I don't think it's going to take us off track, but this
is, I'm going to pose this question as a a hypothesis because I think it's likely to be a little bit of a,
not a barbed wire question,
but maybe like a prickly question when people first hear it,
but it's poses a hypothesis.
You mentioned some of the psychosocial stress issues
based on at the organizational level,
institutional level, societal level,
maybe right down to the family and just life that are
biasing health outcomes for the worse in female populations.
You refer to as the patriarchy.
I'm just trying to make sure that we're both talking about the same thing.
And that's non-exhaustive, I realize, as just a subset of the issues.
I'm also hearing there's a lot more PCOS, which is hyperandrogenization of the ovary.
In, we're talking about, you mentioned, you know, excess testosterone, which females naturally
have more testosterone than they do estrogen anyway, but we're talking about elevated levels.
Here's a hypothesis.
One hypothesis would be that the increased androgens and the PCOS are a consequence of the psychosocial conditions that are
I don't say forcing but are biasing the need for
females to
think behave react act in certain ways to
survive let alone thrive.
Is that a, I don't say this for any kind of political
correctness hypothesis, this is a, in my, this would be a
fun, interesting and I think important study to run, right?
Depending on stress and the conditions that this specific
type of stress do females under produce or over produce
do females under produce or over produce endrogens,
or is it a neutral effect? Does that make sense?
I love this question.
So let me just paraphrase the last part of it
to make sure I got it.
It sounds like what you're asking is,
could PCOS or at least some phenotypes of PCOS
be a response to what I'm calling patriarchy.
And then you add a second part to it, which is do healthy women, like what is their production
of testosterone like?
Is that right?
Yes.
And with the acknowledgement, I mean, you're the expert here.
You're the physician clinician and expert in hormones, and I'm not.
But with the understanding that absolute levels of hormones are interesting,
but perhaps not as interesting as the ratios of testosterone to estrogen.
So, when we're talking about excess testosterone, we're really not talking about, oh, women
making a lot of testosterone because, frankly, they already make a lot.
Like, then most people that weren't aware of that, I wasn't aware that women make more
testosterone in estrogen.
And we need it.
Right.
And so, it's not saying that testosterone in women is bad or is always a reaction to
the environment.
Yes.
But when it becomes super physiological or hyper elevated, I could imagine all sorts of
social conditions that would create that.
So in males and females, but here we're talking about PCOS and females in particular.
So I'd love for you to speculate, should we run the study?
We should totally run the study because I don't know the answer.
I suspect that you're onto something.
It may not explain all of the women with PCOS because as I mentioned, there's a lot of
different phenotypes, but I think it could explain a significant portion.
And you know, you're almost, you're seeing if we look at the gene environment interface,
this environmental influence of having been someone who's got power over you, if PCOS
was a response to that, the way that we treat it would be completely different.
So on the one hand, I want to be careful not to dismiss the suffering and experience of
women with PCOS.
I've got a lot of women with PCOS in my family.
And it is, there's so much pain and suffering, you know, especially if you want to have a
baby and you try for years and you just can't ovulate.
On the other hand, I read a paper recently and maybe we could cite this that compares
the phenotype of a woman with PCOS to a man who is hypo antigenic. And I think that's a really interesting way to look at this,
because the thread we haven't talked about with PCOS
is the role of insulin and glucose.
So for some of the phenotypes of PCOS,
the problem is hyper insulin,
emia, high insulin in the blood,
is driving those thiccoselles
in the ovaries to overproduce testosterone.
These women are insulin insensitive, so more insulin is being cranked out, and these cells
in the ovary are therefore making more androgen.
You don't like to say insulin resistant?
Oh, I can, I don't have a problem saying insulin resistant.
Okay, I just, I like the way that you do it.
And just, I'm just a little bit outside the lane lines of my expertise.
So I was trying to use it.
What is the correct nomenclature so that we can make sure?
Well, what I like about insulin insensitive, the way that she just said it, is that I think
that offers people a way in.
And I love to do that in terms of messaging.
Insulin resistance starts to lose people because they don't really get what that means at a receptor level.
I think I say insulin insensitive because when people hear insulin sensitive, it almost
sounds like a bad thing, but that's actually what you want.
So I think that's how I defaulted to insulin insulin.
What's your insulin?
I don't know.
What?
I'm due for a blood test.
Yes, you are.
I'm due for a blood test.
I had blood work done in the eight months.
Sure.
That'd be great.
I'm always experimenting with different supplements and different behavioral regimens,
and I've kept charts since I was 19.
Oh, you're like my patient.
I've been sort of obsessed by this, and I would say everybody, if you can afford it,
and at the time, actually, I had to save up insurance when cover it, get some basic blood
work done so that you have a reference point.
Do it as soon as possible possible because even, you know,
the, we've been talking about these women over the life cycle.
I wish I knew what my insulin was when I was a teenager.
I wish I knew what my fascinating insulin was.
I really wish I knew my post-prandial insulin,
like in my teenage years, in my 20s, in my 30s.
Well, I knew it at my 30s starting at 35.
Are you a fan of continuous glucose monitors?
The you just most gigantic fan of CGMs.
I've never seen any tool that I've ever used in medicine change behavior
the way that CGMs do.
Wow. Why do you think they are so effective at changing behavior?
I've tried one and I really liked it.
I learned that in the sauna, my insulin, my blood glucose goes up probably by a bit of dehydration.
I learned what kind of foods work for me, which don't.
I thought it was fascinating.
However, behavior you could possibly imagine
is that your imagination impacts blood glucose.
Totally fascinating to me, including how
two wake up during the middle of the night versus one,
versus none impacted blood glucose the next morning, fascinating for a dataie like me is like I was in heaven. Why do you think they are so effective
in changing behaviors? Is it because of that that people can see that real-time control like
scan in and like oh that's the that's the sandwich. I think it's I think it's many things I think it's
generally the enchantment of learning about your own chemistry. I love that. And I think it's generally the enchantment of learning about your own chemistry.
I love that.
I love that.
And I think for me, what I've seen, I feel like doctors are basically marketers, like
the sacred marketing, like our job as a physician is to convince people to do something that we
think is good for them based on the best science.
But we can't just say, here I want to fill this prescription for a CGM.
You have to market it. You have to say, I think this completely changes the way that you approach your prediabetes.
I think this could dramatically affect your risk of Alzheimer's disease.
It's just so worried about the term other has.
So our job as physicians is to be that sacred marketer.
So CGMs are one of my tools that I think are so crucial.
So enchantment number two, yeah, it's the real time effect.
So if you go get your glucose and insulin measured, or maybe you do like a two hour glucose
challenge test, where you look at glucose and insulin at the fasting point one hour later, two hours later or more frequently,
that does not have the same kind of behavior effect as having continuous data where you can say, okay, I drove to see you Andrew from my place in Berkeley and
it was stressful, it was trenchily, and I know my glucose was elevated.
Like I think really understanding what the meat eaters are of your glucose control is essential.
Now that said, it's also kind of a later effect.
I mean, I'd rather know your insulin.
And we know from the Whitehead White Hall study that insulin, especially post-prandial insulin,
Vastuinsulin 2, can change years and years before you get a change in glucose.
So that's more for predivities and diabetes.
So I think those are the main reasons why I think it's such an important tool.
Third thing is it democratizes data, which you do too.
I mean, incredible how you do that with your podcast.
But I think one of the most hopeful and exciting things that I'm seeing right now in the
health space is that we're going from this patriarchal relationship where doctors hold the power and are the gatekeepers of data to
patients and clients having much more access to that enchantment about their own chemistry
and their own biology.
So to me that is so exciting.
Like for me to be able to, I've got, you know, probably 100 patients that are in a data stream with me where we're
looking at their glucose.
And I can, I mean, I'm on spatical, so I'm not doing this so much anymore, but I can call
a patient be like, why is your glucose so high?
Like, what did you do?
Oh, it was my birthday.
I had a piece of birthday cake.
Like that kind of collaboration that also is teaching the patient to be their own clinician. To me, that is a
loop of benevolence and integrity that I think is essential to creating health. We've got a
disease care system. We need the democratization of data to become a health-based system.
Amen to that. A million times over. We share that sentiment at the
contel at a deep level. I think the pandemic actually assisted in, well, it harmed
many things, but it assisted in people's understanding that no magic fairy nor the government nor any,
anyone was going to arrive at their door with a kit of things to make them healthy, that provide sunlight, movement, sleep, and all the various aspects
of nutrition.
No, nothing.
Nothing that everyone has to have access to first and foremost, and then implement those
things as best they can.
Speaking of which, and kind of circling back to this idea of people in their late teens,
20s, 30s, and onward, if you had a magic wand and you could give two or three don'ts, or to make it personal
if you could go back in time and erase certain behaviors, what would the don'ts category
be?
You couldn't tell us more than two or three, but if the goal is to maximize vitality and longevity.
And those are not always parallel to one another.
It's certainly not the same thing, sometimes orthogonal,
but let's just say fertility being a proxy
for vitality and longevity.
I think people will sometimes forget this,
that fertility isn't just about people
who want to conceive children,
it's also, it can serve as a proxy for vitality and longevity.
So what would you like to see patients?
Let's focus first on female patients, but if it extends to male patients as well, what
would you like to see them not do or do far less of?
I really like that.
So I would say a few things.
I'll just headline them and then we can go into detail. Number one, sleep. I do want to diverge from you a little bit on some things,
but sleep is probably not one of them. No, well, feel free. I mean, you're the one
that worked 100, you know, on the work to 100, 120 hours a week, you know. I can't imagine
unless you lived in a different reality than I do. And there are times in my
career where I was pulling all nighters and sleep depravars.
Just, I don't recommend it, but I did it.
Yeah, I hope you don't do that anymore.
No longer if I can avoid it,
but there were years, many years where it was like,
all right, here we go.
And I'm quite adept at it for one cycle.
Yeah.
But two nights I kind of start to fall apart.
Totally.
So I would say sleep, alcohol, high perceived stress.
And I'd love to talk about maybe the data
and telomeres and what we know.
So you'd like to see people get enough sleep.
So don't just.
Yeah, not all of these are concordant.
So not enough sleep, too much alcohol, too much perceived stress, eating the wrong foods,
toxic relationships,
and isolation.
And then number six, not moving enough,
or not moving and exercising in a way that really fits with your body.
So we start with that one actually, just because it's such a moving enough or not moving and exercising in a way that really fits with your body.
So we start with that one actually. Sure.
Because it's such a, and then work backwards.
That's interesting.
I, I, I think nowadays people appreciate the need for quote unquote cardio.
I know that the exercise physiology is cringe and, and dissolve into a puddle of tears when I say that,
but getting the heart rate up over some period of time
longer than 10 minutes in order to generate cardiovascular health circulation. So and resistance training of some kind, maybe flexibility. What do you mean by body phenotype or
and exercise? I'll speak from personal experience. So what I did through, I mean, I gave up my 20s to medicine. And during that time, I occasionally got to the gym,
you know, at UCSF, I'm pronouncing, so you could go to the gym, and then as soon as your
beeper went off, you're back into Bosville. But I didn't exercise much. I had, um, do you
remember Nordic tracks? I had a Nordic track in my house, and that was, that was like it. What I believe, because for me, the primary
outcome that I'm interested in is cardiometabolic health. So when it comes to exercise, what
I really feel if we're going to be at a population level, I feel that about a third cardio, two
thirds resistance training is based on my synthesis of the literature, the best
combination.
And I think there's, you know, as you described with your sign study, I think there's a minimal
effective dose, which for a population is about 150 minutes.
I think most of us need a lot more than that per week per week, but I think you know for me
because I have a phenotype
that
produces a lot of insulin kind of depending on
how I'm on my game. I have a lot of glucose, so I have to exercise a lot more to dispose that glucose.
So I think you then have to move from
medicine for the population or to dispose that glucose. So I think you then have to move from medicine
for the population or prescriptions
for the population to what works for the individual.
I think that recommendation is fantastic.
I think resistance training, well, let me put this way.
I'm neither a trainer nor a physician,
but I've seen in family members that we're doing.
I wouldn't say a lot of cardio,
but just cardio, when they add resistance training, everything
in terms, including their biomarkers, have improved dramatically, in particular for female
members of my family.
Well, one of the mediators that I think is important, especially for people who do what I call
chronic cardio, which is what I did, is cortisol.
So we know that runners, especially marathon runners, people who do a lot of cardio and
don't do much resistance training, they tend to have much high cortisol levels.
And you can buffer that with vitamin C, vitamin C can decrease the effect, but chronic
cardio doesn't always serve people.
So quick personal example.
When I first started measuring hormone panels in myself, I went to my physician and I said,
I'm 35, I've had one kid, I want to have another kid, I've never been so exhausted in my life.
I just feel like I'm pushing a rock up the hill.
I've got this belly fat that I don't like.
And I don't want to have sex with my husband.
So what do you think?
What could we do about this?
And he offered a birth control pill and an antidepressant.
And a goodness.
So I left him and I went to the lab and I ran a hormone panel.
And my cortisol was three times what it should have been.
My insulin was in the 20s, I was fasting.
My glucose was 105.
My thyroid was mildly abnormal.
My progesterone was low.
And that set me on this course of realizing that
what I was doing as a physician,
taking care especially of women, was not
getting to some of these root causes that are so essential.
And I would say I had to start first with cortisol.
At that time I was running four miles three times a week, four times a week.
That was just racing my cortisol further.
So that was not the right exercise for me.
I needed more adaptive exercise.
I started doing Pilates, more yoga.
That helped to lower my cortisol.
I mean, it started me on, you know, changing the way I was managing perceived stress
and it also changed my supplement, Richmond.
Can we talk about that?
With the moment you said, a lowering cortisol thought of the two supplements that come to mind are
ashwagandha, which I think can potently reduce cortisol, but I've heard some recommendations
about cycling it. And I've always wondered about time of day for
ashwaganda and take because it's sort of quote unquote want.
Cortisol elevated in the early part of the day. Yes. And we know
this. We know you do not want cortisol peaking later in the day.
No, you do not.
interferes with sleep.
interferes with sleep. Interferers with sleep.
And then the other supplement is rodeo rosacea.
Do I have in my pronounce in that correctly?
Yeah, so rodeo is very effective.
It's been shown in multiple randomized trials
to lower cortisol, so that could be very effective.
What sort of dose?
I've started taking it recently, by the way,
and I made a huge mistake.
I like to make the mistakes first,
so then my audiences don't make them.
As I was taking it, I heard it was in adapted genes,
so I thought, oh, I'll take it before resistance training,
but of course, you want the cortisol peaked
during resistance training, because that's gonna set
in motion the adaptive response.
So I started taking it later in the day,
and it's really improved.
I would say my late day, second half of the day cognition,
this is subjective, to be fair.
I just feel like a minute more even playing of attention in the second half of the day cognition, this is subjective, to be fair. I just feel like a minute more even playing of attention in the second half of the day.
So you're describing an end of one experiment, right?
Anachdata.
Well, it is not anachdotal.
So I was taught at our medical school that the hierarchy of evidence starts at the lowest
with expert opinion, you know, case studies, then you've got cohort studies, then you've
got observational data that's prospective, then you have randomized trial. But the highest quality
evidence of all is the end of one experiment, where you serve as your own control. So what you're
describing with Rodeola, I would frame that as an end of one experiment, where you have a wash-out
period and you compare before and after, and I'd like to measure some other metrics
to see if there's an effect, including your cortisol.
So, rodeo has been shown in multiple randomized trials
to reduce cortisol.
The other thing that I think is super effective
is phosphatidal serine, PS for short.
Fisual also more modestly reduces cortisol.
Ashwagandha is interesting.
So in my first book, The Hormone Cure,
which I read by the way.
You did.
I was hoping that was the one you read.
I did, I read it and it's spectacular.
And I thought going into it,
I had this like, you know, let's just call it what it was.
It's kind of male bias.
Like is there gonna be anything in here for me?
Because I don't have ovaries and you know, let's just call it what it was, it's kind of male bias, like, is there gonna be anything in here for me? Because I don't have ovaries and, you know,
is this gonna be, and it was immensely informative.
So thank you.
Yeah, I have very fun recollections
of the walks I took listening to it,
and then I own the print version too.
So I like to switch back and forth.
So thank you for that.
It's just a superb book for anyone to read.
Thank you.
I so appreciate that.
So in chapter four, you may or may not
remember that Ashwaganda, at least the time that I wrote that book, Ashwagana's data is not great,
but lack of proof is not perfect against. So with Ashwaganda, most of the data comes from thousands
of years of using it in diabetic medicine, and it's considered, again, not my science hat. It's considered
a double adaptogen so that it's potentially helpful when you are a high cortisol phenotype
like I was, like I sometimes still am, or low cortisol. I haven't found that in my patients,
although I'll give you one exception. So Ashwagana is mostly based on animal studies. There is not as much human data, but it is used a
ton in integrative medicine. There's one supplement that I found to be
incredibly helpful for people who tend to have high cortisol at night, and
that's called a cortisol manager. It's by integrative therapeutics. I don't have a second
supplement manufacturer that makes something similar. It's their number one selling supplement because
it's so effective. Is it a cocktail of several things? It's a combination of phosphatidyl
serine and ashwaganda. Tell me more about phosphatidyl serine. I am familiar with it for, it's been mentioned
by some guests that were on the Tim Ferriss podcast long ago for other
reasons. I think related to sleep. Yes. And maybe that's another reason why you like it.
But before we move on from rodeo lab, is there a dosage of rodeo lab?
So I would refer people to my book because the randomized trials and the doses that were used
are in there. So I can't remember with rodeoola, although I took it this morning to prepare to be with you.
We can look it up and put a show note caption
to be completely clear.
I can remember the dose with phosphatiles here
because I take that regularly.
So 400 to 800 milligrams is the typical dose for PS.
And what's interesting is that in the randomized trials
that were done, 400 milligrams was more effective
than 800 milligrams. Interesting. I've found that for several supplements that the 400 milligrams was more effective than 800 milligrams.
Interesting. I've found that for several supplements that the lower dose was more effective.
Yes.
Yeah, I won't, it doesn't matter what those were. And so when you say, if PSU were referring
to, by the way, folks, not PCOS, just because scientists and clinicians are familiar
with, and military, very familiar with acronyms, phosphatidal serine, PSA, 400-800 milligrams,
400 being more effective,
taken later in the day, or early day, does it matter?
It depends on when your cortisol is high.
So for me, I tend to, you know, what's the pattern for cortisol?
Typically, it rises to its peak 30 to 60 minutes after you get up.
Then it has this gradual, kind of asymptotic decline until you go to bed.
So if you're someone like me who peaks like way crazy high, I don't do that anymore,
but that's what I used to do. I need a phosphatideous hearing in the morning.
For people who are high at night, who have what's known as a flat cortisol pattern or an inverted pattern,
you wanna take it at night.
And the flat pattern, just quick sidebar,
is that that's associated with a number of conditions
that most mainstream physicians don't know about.
So a flat pattern where it's low in the morning
and it's high at night is associated with anxiety, depression,
decreased survival from breast cancer that was studied at Stanford by David Speagle.
He was my close, even collaborator, even on the breathwork study that we do.
Oh, interesting.
Yeah, he's our associate chair of psychiatry now.
So a wonderful human being has been a guest on this podcast and I'm now fantasizing about a conversation that includes a panel of incredible minds like you and David from the clinical side.
So in any case, yeah, the late shifted cortisol not good. Not good. And it seems to
have the worst immune downstream issues of any of the cortisol patterns.
So that's really important to know about because it then maps to things like it's related to PTSD.
So that's the pattern we see like in vets who've got PTSD as well as others.
It maps to autoimmunity. It maps to fibromyalgia. I was told that one in 12 people
have our heterozygous, so one mutant copy,
or hypomorphic for some mutation in adrenal related genes.
So congenital adrenal hyperplasia, is that true?
And if so, that means that one in 12 people walking around are
cranking out far too much cortisol or not enough cortisol or the cortisol system
is already skewed in a direction that makes life more challenging at the
levels we're talking about. Did I hear that correctly? Because that one in
12 is not a small number. It's not a small number. It fits with what I see
clinically. I mean, I want to see that data just to see,
what does that mean?
And could you modulate it with environmental influences?
But it certainly fits with what I see.
I was taught once again in mainstream medicine
that in terms of adrenal function, it's very binary,
how most clinicians think about it.
You either have Addison's disease and you don't make enough cortisol or you've got cushions
or cushing wood pattern and you make too much cortisol and anything in the middle is normal.
And my experience is that, hell no, like there are those of us like me who make a lot of
cortisol, I don't have cushions.
Maybe I've got one of these. I wouldn't call
it a mutant gene. I would call it more of a vulnerable gene. So maybe I have one of those.
Maybe that's part of the reason why I make two to three times what I should be.
I'm aware of certain groups of individuals from within the military sector that have, there's a more frequent occurrence of some mutation in CAH,
can you general adrenal hyperperpegian?
Not necessarily two copies,
which if people look that out, they're gonna go,
oh wow, there's all these phenotypes.
And but, sort of hypermorphic type things,
so you don't less than, or too much cortisol,
and they are very good at staying up multiple days per night.
Right.
Multiple nights in the series. So they can pull all nighters very easily.
Yeah.
They can push harder when most people would quit.
And everyone thinks, well, that's a great phenotype to have, but guess what?
It's because they hyperproduced cortisol.
Yeah.
And so that's interesting.
And I think if we were to panel medical students and graduate students and you were to look
at, you know, who's pulling excessively long hours, who's stressed out a lot, even outside
of academia and medicine and pushing, pushing, pushing really hard, I think the ability to
push and not crash.
We think of it as adaptive, but in some sense it's maladaptive over a series of years,
which is for what you described earlier.
Yeah, it's such a good point because, you know, you, in some ways, you want to
select for that in certain professions like in the military, like in medicine.
But I would wonder for those folks about the downstream consequences of producing
so much cortisol.
No, it's got to be detrimental for their health. It's got to be detrimental for their health in the long run.
And you see that.
But even the data shows that if you're someone like me who makes a lot of cortisol,
higher rates of depression, like 50% of people with major depression have high cortisol levels,
higher rates of suicide, much more metabolic dysfunction.
We know that trauma as an example maps to an increased risk of glucose,
metabolism issues, and certainly high cortisol does that because it's one of the jobs of cortisol is
to manage glucose. And it's, it kind of sets you up for this one number five, which is toxic
relationships.
Someone who hyperproduces cortisol,
it's hard to live with someone like that.
It's also, I would say people that have this,
let's just call it biological resilience.
It's not always adaptive
because you can stay in bad circumstances longer.
The ability to crash,
provided it's not suicide or life destroyingdestroying or long arc of pause and the
requirement to take two years off from work or school or something. The ability to keep
pressing on is a double-edged sword. Let's put it that way. I want to make sure and
insting within this conversation, because you mentioned Fossil D'Ailles-Siri and we talked
about Rodiola, Rosacea, we talked a bit about ashwagandha, you've also talked about omega-3s and fischoil
in particular.
I'd love to know your favorite sources of these.
I think nowadays there's more general acceptance that getting these essential fatty acids
is important.
Do you have a threshold level of sort of grams?
I've encouraged podcast listeners to consider, depending on what they're eating, to try and
get a gram of EPA or more per day.
Does that seem excessive?
And what are the real data on EPA's?
Because then the cardiovascular experts always hit back and say, oh no, you know, it's not
good for cardiovascular health and then you know, well, it's better than antidepressants
and other studies and they go, no, so I feel like if you really want
to make your life difficult, you want to raise your cortisol, you go on Twitter and you say
something positive about omega three's a big show.
And you learn a lot.
What are your thoughts on omega three's?
I take a lot of them.
I've always been a big fan.
Yeah.
So this is where I personalize.
I think some people need more than others.
And what I do is I measure your level. So this gets back to nutritional testing. So for
you, I would suggest an omega-quant or one of my favorite Cardi metabolic panels is to
do a Cleveland heart lab. So I think they give me the most reliable information, not just for lipids and subclasses and,
you know, NMR fractionation, but it also gives me an insulin resistance score. It gives me
levels of omega-3s. Great. We'll provide links to these different sites so that people
will know. But one quick thing about that, the whole story is not omega-3s in taking fish oil.
The whole story is not omega-3s in taking fish oil. So the work of Charlie Sirhan at the Brigham is showing that the way that we resolve inflammation,
our understanding of it is really, I think, in the learning to crawl stage.
And so if you look at the Omega-36 pathway in the body,
fish oils can help kind of push the reactions in a particular direction.
But typically they're not enough for the resolution of inflammation.
Now what most people do, including my MBA players, is they pop an ibuprofen
or something like that when they've got inflammation, that's got lots
of other side effects that are not so good for you.
And we know in terms of the resolution of inflammation that taking something like ibuprofen reduces
the amplitude of inflammation by about 50 percent, but then it potentially blocks the
complete resolution of inflammation.
So there's these new supplements that you may have
heard of called specialized pro-resolving mediators. There's a lot of different supplement companies
that make them. And that combined with fish oil seems to be the best combination. And what I do
for athletes who've got, you know, kind of the normal aches and pains of the training load they have is all combine a little aspirin, small dose,
just like 81 milligrams or two of those baby aspirin, together with fissioil plus specialize
per resolving mediators, and there's some that are NSF, they're certified for sports. But the
the dose, I would say with my patients some of them only need
1,000 milligrams your gram that you mentioned for the population some of them need
six grams together with SPM's so I think it has to be personalized
how young
Is it okay for
People to start taking omega-3s
for instance young women in their teens, when they're 20s and they're 30s,
young guys in their 20s and 30s,
should they take fish oil?
If just as a, assuming they're not gonna get anything tested,
I'm thinking about the college student
who is really into biomarkers
and that sort of thing will go do some of this.
But many people won't, but they wanna do the right thing.
So they'll try and drink a little less, hopefully, hopefully they won't smoke or vape. Please don't smoke or vape. The idea that vaping is, okay, it's like we had it all that was so bad.
So bad for everything we're talking about.
Like it's like exactly. So just, you know, hopefully they'll try and avoid those things. Hopefully they'll avoid hard drugs. Hopefully they'll avoid getting any STIs if they do that will resolve them quickly, hopefully.
Yes.
So, but they might say, oh well, okay,
I'm willing to take some magnesium
or take some phosphodilous hearing,
buffer my cortisol, eat some vegetables.
Should they consider taking fissual
as a kind of across the board, inoculatory thing?
So I'd like to rank order these.
I would say fissual, yes. I think a thousand milligrams
as general recommendation is good, but I also have a food first philosophy. So my preference
would be that they're having salmon or some kind of smashed fish, and they're getting
that as the primary source of their omega-3s, and then the days that they don't have fish
I recommend it probably twice a week that they take fish oil. Then I would put magnesium
next since so many people are deficient. Then I'd probably put vitamin D. What how many
IU of vitamin D per day? Well, you keep asking me this like for the population. Well, for the
let me put this way for the lazy for the lazy person or and this is an or not an end or the person
who just doesn't have the finances to go get
measured, levels measured, because in our audience is a huge range.
We've got people who can have tons of disposable income that listen to this, but we have to
be able to notice disposable income.
So, with thousands of two thousand international units, but what I do is I do to a serum
level that's between about 50 and 90. Great.
And so I have a vitamin D receptor SNP, and so I need to take about 5,000 a day to get
to what I need.
A lot of people don't need that.
And you know, there's some supplements that I don't know if they need.
So you mentioned phosphatidyl serine for someone who's a college student and their cortisol
is completely normal
They're wasting their money on P.S. They don't need it. They might need it later
But they don't need it now. I'd like to make sure that we circle back to birth control in particular
oral contraceptive birth control
And we should touch on IUDs perhaps a little bit more but
What are your thoughts on sort on pure estrogen birth control?
This is what I learned when I was in colleges.
That birth control is basically tonic estrogen, so constantly taking estrogen, estrogen women
are taking estrogen, so that they don't get the estrogen priming of progesterone.
You're not getting any ovulation.
And I've known women that have been taking oral contraception
as like estrogen pills basically for five, 10, 15 years.
Are there long-term consequences of this
as it relates to pregnancy, PCOS, menopause,
if so, what are some of those consequences?
What are your concerns? What do you like about oral contraceptives?
What do you dislike about them?
I like how balanced you ask that question.
So, women who take oral contraceptives as long as you're describing, like, 10 years or longer,
we call those Olympic oral contraceptive users.
In terms of benefit, I think that especially when they
first came out and even now, it gives women reproductive choice and that's
essential. As you may know, a reproductive choice has been declining recently.
So I'm a big fan in that regard and we've got a lot of data to show both the
risks and also the benefits of it. So I'll speak first into the benefits
because I'm gonna get on a soapbox a little bit
about the risks.
So we know that it reduces the risk of a varying cancer.
So there's something about this idea
of incessant ovulation that is not good for the female body.
So if you look at, for instance, women who are nuns, who don't take oral contraceptives,
and they have a period every single month of their reproductive lives, they have a greater
risk of a varying cancer.
So if you look then at women who have several babies, and they've got a period of time when they're pregnant that
they're not ovulating and then they breastfeed for some period of time. They have a lower
risk of a varying cancer. So oral contraceptives help with reducing ovulation and reducing risk.
We know that if you take the oral contraceptive for about five years, reduce your risk of a varying cancer by 50%.
And that's significant because we're so poor
at diagnosing a varying cancer early.
There's really no method that's really effective.
We use CA 125 and ultrasound screening,
especially in women who are at greater genetic risk.
But even that, often we diagnose it in a later stage.
Maybe just because that statement is going to highlight for a number of people the question
of what are some of the earliest symptoms that people can recognize without a blood test.
So is ovarian cancer?
Is it going to be pain?
So the problem is the symptoms are so vague and they're so non-specific.
One of the most common symptoms is bloating.
And we've already talked about constipation.
We've talked about how women have this longer track,
GI track, and so bloating is a really common experience
for most women.
You get a bulk symptoms, feeling like your lower belly
is kind of pressed out.
So the way that we inform women in terms of watching for this is to get regular gynecologic
exams for women who are at high risk or they have, for instance, an ultrasound for some
reason and it shows a mass that we're concerned about.
There's a way to triage that in terms of what kind of evaluation that they need and that's
the situation where you might get a blood test called the CA129.
CA125.
Yeah, the problem is the symptoms are so vague.
It could be, it depends on how big the tumor is,
how much bulk you have, what it's pressing on.
So if taking estrogen and thereby reducing
the frequency of ovulation lowers the risk of
ovarian cancer, should women that are, even women who are not sexually active, so they're
not actively trying to get pregnant or avoid getting pregnant, but if they're not sexually
active, then the probability of conceiving unless they go through some IUI or some other
route is very low, as far as I know.
So I was taught in high school anyway.
Would they be wise to suppress ovulation for periodically using hormone-based contraception
just so that they can offset the risk of ovarian cancer? That's a very rational question,
and I would say that's what mainstream medicine has had at its back to recommend oral contraceptives,
not just for women who are seeking contraception, but for acne, for painful periods,
for really kind of the drop of a hat, they're prescribing oral contraceptives. That's what I was talking to.
But there are so many consequences. And I think the issue here is more about consent because
in OBGYN and I started out as a board certified OBGYN and I now mostly see men but I
was taught as OBGYN to
convince women to go on the oral contraceptive and I think a lot of that is pharmaceutical influence
so
Maybe we could talk about the risks
and why the answer is no to your question.
As we do that, could I just ask,
is the so-called ring,
the new, it used to be called the new for ring,
maybe that's a brand name,
but when I was in college,
it was always a discussion about the ring, right,
by both men and women, for reasons that don't belong
on the podcast.
Use your imagination, folks.
So the ring, obviously, it's not oral hormone contraception,
but it's hormone-based, right?
The ring is releasing estrogen locally
as opposed to taking it orally,
but would you slot it under what you're about to tell us
in terms of the concerns?
So we have less data about the ring.
So the oral contraceptive is two hormones.
It's ethanol esteridile and it's a progestin.
So it's not the normal progesterone that your body makes,
the trovers make, and your adrenals make.
It is a synthetic form of progesterone.
And it is the same progestin, similar, same class that was
shown to be dangerous, some provocative in the Women's Health Initiative. So I'm
not a fan of progestins. I do not recommend them for any woman unless the
consequence of not taking them is surgery or some other, you know, unless it
gives them some freedom in some way.
So I don't like progestines.
The new verine is estrogen plus progestin, but it's released transdermally through the
vagina. So given the way that it's delivered to the vagina, the
doses are lower than what's taken orally. But in terms of some of the risks that I'm
about to talk about, we don't know about much of the data. We think that it's similar.
There's probably a spectrum of risk and the new varying is a little more towards the middle
than, you know, what I'm talking about with
world contraceptives. Are you ready for that? Yeah, I'm ready for the risks. Okay, so like with almost any
pharmaceutical, the oral contraceptive depletes certain micro nutrients. So magnesium, there's certain vitamin Bs that are depleted.
It also affects the microbiome.
That data is not as strong, but there seems to be some effect,
and there's also an increased risk of inflammatory bowel disease in autoimmune condition.
It increases inflammatory tone.
So the studies that I've seen increase one of the markers of inflammatory tone
high-sense to BCRP by about 2 to 3x. It seems to make the hypothalamic pituitary
adrenal axis more rigid so that you can't kind of roll with the punches and
wax and wane in terms of cortisol production the way that you can't off the birth control pill. It can affect thyroid function.
I'm thinking of the slide that I have that has like 10 problems associated with
oral contraceptive, but that's what I can remember right now.
That's very helpful, and it makes me wonder whether or not,
if on the one hand, oral contraceptives are protective in women,
it's a varying cancer, but then they have these other issues.
Yeah, there's one other I want to mention.
Please.
Anytime you take oral estrogen, it raises sex hormone binding
globulin.
And you've talked to other podcast guests about this, Kyle, I think,
sex hormone binding globulin, I think of as a sponge that
soaks up free estrogen and free testosterone.
So when you go on the birth control bill,
you raise your sex hormone binding clobulin.
It's soaks up especially free testosterone.
And for some women, it's not a big deal.
They don't notice much of a difference.
But then there's a phenotype,
maybe related to CAG repeats on the Androgen receptor
who are exquisitely sensitive to that decline
in free testosterone.
So this then opens the portal of talking a little bit
about testosterone and women.
So we've mentioned already that it's the most abundant,
biologically the most abundant hormone in the female system,
even though men make almost 10 times as much,
or even more than 10 times, it is so important for women.
It is essential to use so many things, not just sex drive and muscle mass and seeing a
response to resistance training, but also confidence and agency.
And so those women who are so sensitive to their testosterone level, they've got this
high sex hormone binding globululin, their testosterone declines.
What they describe is vaginal dryness,
maybe a decline in sex drive.
But there's also this bigger issue related to confidence
in agency, even risk-taking from studies
that we've done with MBA students,
that I think is a serious problem.
Maybe the most important out of all of these things
is that I can shrink the clitoris by up to 20%, 20%.
And that includes a regression of the nerves
that the clitoris, is that, I mean,
that's a very good question as a neuroscientist.
Yeah, I would think,
used to teach the neural side of reproductive health.
We need to do a series on sexual health.
Maybe you would co-host that with me.
We could certainly use your expertise.
I think, yeah, that's a traumatic number.
It's traumatic.
Yeah, but then let's go back to the sacred marketing.
If I've got a woman that I think should not be on the birth control pill, maybe she's
just taking it for acne or she's taking it because her periods were a little painful.
What I'm going to do is say, let's leverage these other ways of making your period less
painful.
Let's take the message of your painful periods and figure out, okay, it's your inflammatory
tone and we give you some visual and SPMs, maybe a little aspirin when you've got your period.
Like let's find some other ways to deal with it.
Then to take the oral contraceptive which you have not received informed consent about, because it
can trick your clip by up to 20%. Now that usually convinces most people to
come up with it. The elevation in sex hormone binding
globulin does not seem to go away when you come off the birth control pill. To me,
that is the biggest problem with prescribing oral contraceptives.
Now, the data that we have is limited.
There's one woman who, Claudia, something, something,
who looked at sex hormone binding globulin,
a year out from stopping the birth control pill,
and it was still elevated.
It wasn't as high as it was when they were on the pill,
but it was still elevated. It wasn't as high as it was when they were on the pill, but it was still elevated.
So your question about reversibility,
I don't know if we know the answer to that.
Wow, okay.
That's a significant statement
and something that for consideration related to this,
although this might seem not related, it is.
How early do you recommend that women go get their
follicle number assessed in other words to get a size a sense of the size of the ovarian reserve and their AMH
levels measured
I'm gonna I'm an amateur outsider as I say this but we we have an episode on fertility where I just described the
ovulatory menstrual cycle. Yeah. And I'm not the best person to answer that. Yeah, well, we can
too far out from it. Okay, well, I suppose then from taking the perspective of somebody who
thinks about fertility in terms of at least congruent with vitality and longevity,
given that it's fairly non-invasive,
it's an ultrasound or a blood draw for AMH, or both.
Is there any reason why a woman would not
want to get her follicle number assessed
or her AMH levels assessed?
Is there any reason why?
Because I was shocked to learn that most women don't do this
until they're hitting their late 30s or early 40s
and they either haven't conceived
or they suddenly decide that they wanna conceive
and I thought why doesn't every doctor
insist that their female patients have their AMH level
addressed so that if they need to-
It's cost, it's cost.
It's cost.
Yeah, so I think if you've got the disposable income
to do it, go for it.
It's not included in a standard blood panel.
No. No.
Wow.
The only women in my practice who've had AMH has done
and have looked at their follicle count are women who
want to freeze their eggs or in that requires disposable income.
Or they are having trouble getting pregnant.
So they are in the reproductive endocrinology system
and they're getting an evaluation.
And then they're also the women
who have symptoms of early menopause.
So premature ovarian insufficiency,
which is before age 40,
those are the women that I see getting attested.
And I think you're right,
that it should be offered
more broadly.
It speaks to the democratization of data again.
And I think most women don't know that.
So you're doing a huge service, I think, to be speaking into this.
One other point related to that is that what I see in conventional medicine
is that when a woman asks for a hormone panel
and she's not trying to get pregnant,
she usually gets told that hormones vary too much.
It's a waste of money.
You don't need it.
Or if you're feeling hormonal,
when are you going to birth control bill?
Unless she's trying to get pregnant.
If she's trying to get pregnant, suddenly those same tests are very reliable.
And they get their testosterone, their free testosterone, their thyroid panel, they get
their estrogen and progesterone, maybe they get their cortisol, they get their amage.
So there's a double standard between those who want
to get pregnant and those who don't,
and that needs to end.
Yeah, I totally agree.
As I've learned more about
the ovulatory cycle and AMH
and the antropopulation of follicles,
it's fascinating, it just seems to me,
wow, relatively straightforward test.
One definitely invasive ultrasound, but.
I don't consider that.
Yeah, not terribly invasive, but invasive,
at least, but the other one just pure blood test.
Just seems like why wouldn't I would this be offered
a covered by insurance or, you know,
that anyone that wanted it?
But now, now I understand why.
You mentioned menopause.
Huge topic, enormous topic.
We had a guest on the podcast who's not a clinician
who said something in passing, so I want to, I'd likely to get this wrong. But what they
said was that the results of the large scale trials on hormone replacement therapy for women
for menopause said something to the effect of if the hormone therapy was started early enough,
it was very beneficial for vitality and health outcomes,
whereas if women went through menopause
and then initiated the hormone therapy,
hormone replacement therapy,
that it could be detrimental to their health.
So first of all, do I recall that statement correctly?
And then second of all, what sorts of hormones
are being replaced?
Is it just estrogen?
And how is that done?
Is it done through birth control,
oral contraceptives, new vorings?
What are your thoughts on menopause?
When should people start thinking about it?
And what is the palette of things available
so that we can do an entire episode with you on this topic
in the future.
But just to, you know, I get a lot of questions about this. And I'm guessing based on everything
you've told me today that there are women in their 30s that while they may be 20 years out from
menopause, probably should be doing things now in the anticipation of that. Yes. So we haven't
talked about the 30s something, but I totally agree with you. The more you know about your phenotype, your hormonal phenotype when you're in your 30s,
you're set up in terms of what to do in the future, especially things like your thyroid,
your estrogen and progesterone levels, because you can replace to a state of youth thyroid,
whatever that is for you.
You can replace, I don't usually go exactly
back to where the estrogen and progesterone levels were, but we can get pretty close.
So in your 30s having a base case, I think is really essential.
So you spoke to the Women's Health Initiative, which was published in 2002, and we went
from a huge number of women taking hormone therapy to a very small percentage,
like in the range of 5%.
And that means we've got millions, millions of women who are suffering needlessly with
things like insomnia, difficulty with their mood, difficulty with sex drive, feeling
like they are closing the store in terms of sex because they're not on
hormone therapy. I would agree with the statement that you made that hormone
therapy particular forms that are similar to which your body always made when
it's given judiciously at the right time typically within five to ten years of
menopause which is 51 to 52. that is incredibly safe. So it's a complicated
study, the Women's Health Initiative, but it was the wrong study in the wrong
patients with the wrong medications and with some of the wrong outcomes. So it
was powered to look at cardiovascular outcomes. It was not powered to look at
breast cancer. It was stopped because of breast cardiovascular outcomes. It was not powered to look at breast cancer.
It was stopped because of breast cancer risk.
But what happened in the control arm of the study
was that they had an incredibly low rate of breast cancer.
And so as a result, they ended up having
this increased risk of breast cancer at five years
and they stopped the study.
Now, the study was done with synthetics. It was done with conjugated equine
estrogen known as Premarine and Madroxia progesterone acetate. Those were the so-called
estrogen and progesterone. Those are synthetic hormones. We think, especially
the progesterone is associated with the greater risk of breast cancer, although the subsequent
re-evaluations of the data now 18 years out have shown that this problem with the control
group and no increased risk of breast cancer.
And for the women who got estrogen only, those who had an hysterectomy, the premerin, they actually had a decreased breast cancer risk and decreased breast cancer mortality.
So there's a lot to be said about this. I'm trying to keep it really brief, but if you look at the women 50 to 60, so within 10 years of menopause, they're the ones who seem to have the greatest benefit.
So they had decreased subclinical atherosclerosis, so less cardiovascular disease.
They had an improvement in terms of bone health, less progression to diabetes, and then
over the age of 60, they started to have greater risk of certain outcomes,
such as cardiovascular disease, myocardial infarction, and so on. You asked about,
what do I do? And to me, this problem is not just menopause. What's more interesting is to talk about parry menopause.
So parry menopause is the period of time before your final menstrual cycle.
And for most women, depending on how it's tuned to your art of the symptoms, it can last
for 10 years.
So I'm still in parry menopause.
It's been like 20 years because I've been tracking it so carefully.
It usually gets kicked off by having your cycle get closer together.
So that could happen in your 30s or your 40s. You go from 20 days to 25 days. That sort of thing.
You may notice that you start sleeping more poorly because progesterone is so important. You talked about that with Kyle.
You may notice it as more anxiety, difficulty sleeping, and that
probably is related to the estrogen receptor. So, your alpha is estrogen receptor alpha is angioseo,
it increases anxiety. ER beta is associated with an angiolitic activity, and then there's a total of about six estrogen receptors now.
There's the G-protein coupled estrogen receptors
and those are mixed, angiolidic, angiogenic.
So there's this whole period of perimenopausal
and what's most fascinating to me,
and we've got to talk about this either today or another time,
is that there is this massive, massive change that happens
in the female brain that people are not talking about enough.
And so looking at the work of Lisa Moscone at Cornell from starting around age 40, there
is this massive change in cerebral metabolism.
So you can do FDG PET scans. You can look at glucose uptake.
And there's about, on average, a 20% decline
from premenopause, up to age 35, to perimenopause,
to postmenopause.
The women who are having the most symptoms in perimenopause
in menopause, the hot flashes, the night sweats,
the difficulty of sleeping, those are the ones who have the most significant cerebral perimenopause, the hot flashes, the night sweats, the difficulty of sleeping.
Those are the ones who have the most significant
cerebral hypometabolism.
So it's almost like a,
I don't wanna scare people with this language,
but it's a low level, or let's call it pseudo-dimenshoffs,
or it seems to be a phenotype that you can then map to Alzheimer's disease because that's
Lisa Moscone's work.
She's looking at, okay, Alzheimer's disease is not a disease of old age.
It is disease of middle age.
What are some of the biomarkers that we can define that can tell you what your risk is?
I've got a mother and a grandmother with Alzheimer's disease.
You can believe I am all over this data.
An insulin resistance.
Huge part of it.
Huge part of it.
As we talked about before, seems to be somewhere in there, which I think when that first,
when that idea for a surface to a few people like really, but then of course, right?
I mean, the brain is this incredibly metabolicly demanding organ.
You deprive neurons of fuel sources,
they, where you make them less sensitive to fuel sources,
they start dying, they certainly start firing less.
It makes perfect sense.
And I think now it's, thanks to Lisa's work,
work that you've done and talked about.
Quite a lot is in your books and elsewhere,
I think it's really, you know, highlighted for people
that metabolism and metabolism
is going to be as important as genes and genomics
when it comes to dementia.
Perhaps especially in women, is it safe to say that?
I think so because we believe that the system
is regulated by estrogen.
So the decline in estrogen starting
around age 40, 43 is kind of the average, seems to be the driver behind cerebral
hypometabolism. The way I describe it to my patients is it's like slow brain
energy. So you walk into a room, you can't remember why, like you just notice that
you can't manage all the tasks the way that you once could.
Things are just a little slower. I say that to women and they're like, I have that. Help
me. This is then circling back to WHOI, where women are scared to death of taking hormone
therapy. We've got all of these women that are marching toward potentially a greater
risk of Alzheimer's disease.
And they have this opportunity in their 40s and their 50s to take hormone therapy.
And they may not be offered it because the typical conventional approach based on WHI is to say,
unless you're having hot flashes and night sweats that are severe, or I'm not going to give you hormone therapy.
And I just want to call that out. I would say no, that is not the way to approach it.
Further, the concept right now in conventional medicine is that hot flashes and
nights sweats are these nuisance symptoms that we will take care of temporarily, maybe
with a little bit of estrogen and progesterone or birth control bill, because it's given
a lot.
Or that they pass.
Or this idea.
Or this idea.
You just suck it up.
Suck it up.
Doesn't matter that you're not sleeping anymore.
Turn down the temperature in your room.
And that's not right, because half-lush is a night sweats.
Or a biomarker of cardiometabolic disease.
They are a biomarker of increased bone loss. They are a biomarker
of changes in the brain. So many of these symptoms that occur in paramedicopause are not driven
by the ovaries. They are driven by the brain. Yeah, it's the bi-directional crosstalk between
the body and the brain keeps, you know, I think is the resounding theme. We had Chris Palmer on
here, a psychiatrist who's talking about ketogenic diet for a mental health. I know
We could have a whole other discussion of and we will I hope if you'll agree to it about nutrition and
As it relates to hormones of specific diets and so forth
But the and that's a question to whether this
problem of cerebral hypometabolism,
could we solve it with estrogen and or increased metabolic flexibility?
So I just wanted to put that in. Sorry to interrupt you.
No, please, please interrupt. I know you're, as long as we're there, I know you are a fan in some
instances of intermittent fasting, time restricted feeding,
and or ketogenic diet to get cells sensitive to insulin, which is not to say, if I understand
correctly, which is not to say that women need to stay on the ketogenic diet for long periods
of time, or intermittent fast for only time restricted feeding for eight hours or six hours
a day, but that by increasing, you said metabolic flexibility, excuse me, but by increasing cells,
sensitivity to insulin and then maybe returning to a more typical eating pattern and periodically
switching back and forth, that might actually be beneficial.
Do I have that right?
Yeah, I love the pulse.
So I feel like it's much more physiologic than, say, going on a ketogenic diet and staying
there for years.
All of the data that we have on the ketogenic diet, it's pretty limited in term inspiration.
You know, the longest players that we have in terms of the data are the folks with epilepsy.
And that's just a different phenotype.
So I think in terms of microbiome effects, diversity,
dysbiosis, some of those issues,
we really don't know in terms of long-term effects.
So I prefer with a ketogenic diet
that it's used as an end-of-one experiment
and that to do it for four weeks.
Maybe you measure biomarkers before and afterwards,
maybe you look at your stool before and afterwards,
and we still haven't talked about stool tests yet.
But you could measure your fasting insulin and your glucose. for an afterwards, maybe look at your stool before an afterwards, and we still haven't talked about stool tests yet.
But you could measure your fasting insulin
and your glucose.
You could just start there, do four weeks of keto,
clean keto, including vegetables.
It doesn't have to be 57 a day.
And then measure it again afterwards.
Since you mentioned stool testing.
Yes.
What is your recommendation about stool testing?
My recommendation, this is again in the field of if you have the disposable income. I usually
start with Genova because they've got a good copay system with insurance. That's what I typically
use. I usually do their one-day stool test where you have to go digging through your stool and set it off to this lab that's in North Carolina.
I usually do the one day unless I'm concerned about parasites. In that case, I tend to do three days. I do that for people who travel a fair amount and go to places where there's greater risk or they just have gut symptoms.
Another test that I do a lot is because I I was like to mention two labs, is a test
by Wingemony. And this is much more of a data-wank type of test because it's powered by AI.
It was designed by a guy who's got inflammatory bowel disease and he is a, he's a PhD deep phenotyping bioinformatics
guy who wanted to make this really easy. So the test is is under the umbrella of
Thorn and these call it gut bio they might have another name for it and they
just improved it so that it's a wipe instead of digging through your stool. And so my athletes will do it now. They were not so
into digging through their stool before. Is anybody really no one is? I don't want
the answer. I know the answer I prefer to that. But that's a super interesting
test because it's you get much more dense data. The issue is with apologies to my friends at Thorn.
The issue is that their recommendations end up
being Thorn supplements.
So that can be very easy for people who want to connect the dots.
That's not always the way that I like to do it.
First of all, three things.
You've shared with us an immense amount of knowledge
and in that first statement,
I also want to apologize
because I threw it you the entire lifespan
of female lifespan, reproductive health,
contraception, diet, microbiome, so many things.
But I first, I just want to say, you've taught me a tremendous amount.
Including, I think something that most people, including myself, have not thought about enough, which is the psychosocial impact on things that we're all familiar with, constipation, bowel movements, what we eat,
what we avoid, I have to say really a huge thank you
for that because it's not something
that's been discussed on this podcast before.
Sort of know that brain communicates with body,
psychology and biology are linked,
but I think this is the first time that anyone's ever
directly linked,
circumstances and biology and psychology in such a concrete
way.
So that's the first thing.
And I know I speak for many people on that.
Second of all, we barely scratch the surface of your knowledge, which is both frustrating
for me because I always want to learn more and I know many other people do as well, but
also very, very exciting because hopefully without much persuasion we can have you back on to talk
about things.
No, for sure at all.
Like men.
I know you're working with men now, men's health, some particulars around, I think there's
more for us to explore in terms of PCOS, menopause, contraception, and all of the above.
But then something that you and I were talking about off camera before we started, which I
think is a really important factor that ties back to this issue of trauma and stress and
the bidirectional relationship between biology and psychology.
Hopefully someday we won't even separate those two.
Which is the use of specific medicines, including plant medicines.
And how that can influence
overall health, which no doubt will include hormone health.
So I say all of that for two reasons.
First of all, to queue up, we won't even call it a part two, but a sequel to this, which
I'm gratified to hear that you'll join us for that.
And then also to just really extend a huge thank you, the amount of knowledge that you've shared is immense and is going to be very, very useful and actionable for men in terms
of their thinking and their actions and for women in particular, today's discussion,
in particular for women, in terms of how to think about their health and biology, how
to think about their psychology and the environment that all of that is embedded in. I just want to say an enormous thank you.
Thank you, Andrew. I so appreciate that. I so appreciate what you offer to the world in terms
of a way and a way to understand physiology and how to craft a architect a better life.
Can I just add one last thing? Because I didn't talk about it since we didn't
get to the 40s and the 50s in those lists of biomarkers. So I feel like if people, if women
went away with one thing today, it would be to do a coronary artery calcium score by age 45
and sooner if you've got premature heart disease. How is that taken? So it's a CT scan of the chest.
You can self-order it.
Like I think it's stamped for hospital.
You can self-order it.
Last time a patient checked it was $250.
So again, disposable income.
But it tells you it almost gives you this fork in the road in terms of how much you need
to pay attention to cardiovascular health as a woman.
And it's 45 for men too.
So if you haven't had one, have you had one? No.
No. in terms of how much you need to pay attention to cardiovascular health as a woman. And it's 45 for men too. So if you haven't had one, have you had one?
No.
You need one.
It's fun, cortisol, CAC.
Great.
So I'll run all that by you.
It's really essential.
And it's, yeah, it's so fascinating because there's some women who have a zero, so my score is zero.
And that's great. So often you can just keep doing what you're doing. But if you're 45 and you're
starting to be elevated or maybe you've got PCOS or you've got some other biomarkers
tending you in this direction toward the number one killer, really eight to nine out of the top 10 killers in the US,
that allows you to really start to make changes.
And I think it's essential to know that data.
It's not, it's probably not going to be offered by your doctor.
Certainly Peter Tia is going to offer it, but most conventional doctors are not going
to do it.
And then the last thing I want to say before you mention it.
So if I were to go to my doctor and I just say I want to a cardiac calcium score.
That's what people are doing.
Coronary artery calcium score.
CAC.
Okay.
So everyone here that and know that if you're 40 or older and maybe if you're 45 or older
get it.
So the last thing is, and this is for men and women, is your ACE score?
So adverse childhood experiences.
Knowing your ACE score is so essential in terms of a baseline for how much trauma your system,
your pine system endured when you were a kid.
And we know that childhood trauma, whether it's abuse or neglect or having an alcoholic
parent, that maps to disease and middle age.
And it can give you so much insight. I'll give you an example. I've got a patient who had
an elevated coronary artery calcium score who does everything right with her food.
I think it was her trauma that elevated her CAC when she was 45. So I think an A-score, knowing your A-score,
starting as a teenager, like knowing it,
and knowing how to work with that is really essential.
There are certain people, they are exceedingly rare,
but you are one such person that when they speak knowledge,
just comes out of them and it's incredibly useful
and helpful knowledge.
So thank you, I'm gonna get both of those things.
Good.
And I highly recommend that everyone else
pursue ways that they can get those
or if they can't get them that they, you know,
you're marked those as things to get at the point
where they can obtain sufficient disposable income.
It sounds like the health,
the detriment to health that those can offset
would be well worth the cost.
Totally.
Thank you.
Thank you for joining me for today's discussion all about female hormone health, vitality,
and longevity with Dr. Sarah Gottfried.
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