The Dr Louise Newson Podcast - 217 - Menopause and the brain: why we need to bridge the gender gap in research
Episode Date: August 15, 2023Regular listeners will know there is much more to the menopause than hot flushes – but how do hormone changes affect your memory, mood and cognition? This week Dr Louise is joined by Dr Dan Reisel, ...Specialist Registrar in gynaecology at University College London and Newson Health Clinical Research Lead, to take a closer look at the relationship between hormones and brain health. Dr Dan says awareness is improving, but researchers must up their game when it comes to studying the female brain. While mood and memory symptoms are common in menopause, too often, studies focus on male brains as they don’t want to deal with the complexity of female sex hormones, he adds. Dr Dan’s three take home tips: 1. If you’re going through the perimenopause or menopause and struggling with symptoms, don’t just accept how you feel. Seek out options for treatment such as HRT that can improve your symptoms. 2. Become an advocate for better care for women going through the menopause – speak to your friends, healthcare professionals and colleagues about your experiences. 3. If you are offered the chance to take part in research seize that opportunity to make your voice heard and improve the experience for women in the future. You can follow Dr Dan on Twitter at @danreisel
Transcript
Discussion (0)
Hello, I'm Dr Louise Newsom.
I'm a GP and menopause specialist
and I'm also the founder of the Newsom Health Menopause and wellbeing centre
here in Stratford-Pon-Avon.
I'm also the founder of the free Balance app.
Each week on my podcast, join me and my special guests
where we discuss all things perimenopause and menopause.
We talk about the latest research,
bust myths on menopause symptoms and treatments
and often share moving and always inspirational personal stories.
This podcast is brought to you by the Newsome Health Group,
which has clinics across the UK dedicated to providing individualised perimenopause
and menopause care for all women.
Today on the podcast I'm really excited to introduce to you,
someone I've known for a little while,
but really respect his brain, his knowledge and his experience.
So Dan Riesel is with me today.
who is an academic, but also a senior registrar in gynecology, but didn't actually train in gynaecology initially.
So we're going to hear a bit about his background and a bit about what he knows about the menopause.
So welcome to the podcast, Dan.
Thanks for having me.
So tell me a bit about your background, because you didn't actually start your first degree, wasn't medicine, was it?
No, that's right. I started life as a neuroscientist, actually.
I like to say that when I was a kid, which is true, I wanted to be a magician.
and instead of pulling rabbits out of hats, I pull habits out of rats.
So I spent quite a few years doing basic research in neuroscience with a masters and a PhD at Oxford in a really exciting lab
looking at the building blocks of working memory in animal models.
And that was work that was part of understanding the brain basis for dementia,
but also for cognition, because working memory is that ability,
to engage in complex tasks and manage different things at the same time.
So it taxes the sort of bandwidth of the brain.
We looked at the particular neurotransmetric glutamate,
but the thing about the brain is that it is an intersection of so many different systems
and so many different neuromodulators and neurotransmitters.
And so what we do in one area impacts in a very significant way,
so many other parts and in so many different ways.
But it was really exciting time doing that.
work and going to conferences and being part of the academic community. But then in the final year of
my PhD, I had a bit of a sort of career think and really felt that although the science and the
academic research was really exciting, it would be even more exciting if I could do that work
in a clinical role, whereas part of a clinical role. And so I went back to school essentially as a
graduate entry medical student at UCLA at 10th age of 28th.
And it was one of the hardest things I've ever done because really then you have to go from not really advanced conversations about the function of, you know, various brain systems to learning basic physiology.
But it was a really good thing for me to go through, I think, because I think it humbled me.
So you're with people that were 10 years younger than you, essentially.
Yeah, it was a group of graduates, but it was a humbling experience.
But I think, you know, coming through it on the other side now, I graduated at UCLA Medical School over 10 years.
ago, it's really shaped me and it's caused me to really feel the impact that when you have
patient exposure, when you really have the ability and the opportunity, the privilege to listen to
people's stories, then really that makes a big difference because it informs how you think
about basic physiology and pathology and about your research priorities.
It's very interesting, isn't it? I, as you know, did some research in a very small scale
compared to you, but I did a BSC in pathology, and I was looking at skin of women who had something
called systemic sclerosis, which is probably a condition you know about, and I was looking at type
four collagen in the skin, in the basement membrane, which is so minute, and I was doing the
technique called in situ hybridisation, where we used radioactivity labels until you know what it is
to mark the different types of collagen. And I got very excited when there was a signal, you wait
two weeks for a result. The first time I did it, I forgot to put.
the right chemical and the right thing. And then two weeks later, there was no results. And I
realised that I would just, because I am a bit cuck-handed. And it made me realise how frustrating
research was. But then also, I got a paper, I got a publication. I was really pleased. I was
working with laboratory people. But then towards the end of my year, I thought, you know what,
I've never seen a patient with systemic sclerosis. I got no idea what they're like. And I'd read about
the disease. Of course I had. So I went up to North Manchester where there was a clinic. And then I
realize these poor women, the skin gets very, very tight, as you know. So the women I saw in the clinic
couldn't open their mouth. They couldn't actually pick up cutlery to eat because they had such
bad scarring and sort of retraction of their digits. And I thought, goodness me, I'm excited because
I found one thing, that's never going to make a difference to their life. How are they ever going
to pick up their children? How are they going to be able to speak? Well, it's quite a progressive
disease. All sorts of things. And I just thought, oh, Louise, what are you doing? Actually, what I really
want to do is sit down and talk to them and work out what it is like and how they can adapt
their life and how. And it's, it is like that with sometimes with research, isn't it, Dan, that
you forget the context of what you're doing it for. I think that's right. I think life in general,
but also clinical medicine is humility school where you really learn from those encounters with
people who are experts on their symptoms and their symptomatology and their condition. And so
one of the things that I love about
gynecology, which is where I'm
worked clinically at the moment, is
the fact that we can
make a difference to women often because
it's a sort of hands-on specialty,
whether it's surgical or medical.
And that is clearly the only way
to make a difference is to really
work on understanding where people come
from. And so I was recently
asked actually, I teach a bit at the
UCL Medical School now.
We were asked to summarize, in
five words, advice to
qualifying doctors. My suggestion was tune into your patient. I don't know if that's five words,
but it is essentially, I think, what I think is the most important thing. You have to tune in
to where they're at, and it's sometimes really hard. It's hard for me as a man to sometimes understand
the impact that gynaecondological disease and pathology and even life stages have on women,
having not experienced it, let alone birth. But that's where really we have to work hard,
I think. It's so important, isn't it? And, you know, when I was younger about 10 years ago,
I was teaching graduate entry.
I was a get course, a graduate entry course in Birmingham University,
and I was teaching medical students then.
And the attitude is very different compared to undergraduates
who had just come straight from school.
And what I realized more when I taught them was this life skill that they have,
which is just, it just takes time, doesn't it, and experience?
And I think having the ability to talk to patients
and understand where they're coming from is the most important thing.
I think it's, well, I know it's such a privilege being a medic and the stories that I've heard,
the way people will tell you things that they've never even told their partner or their best friend
or a member of their family. And they have utmost confidence in you. But it's also having that
confidence that we can share every decision and make sure they're comfortable with it and the art of
communication, but also changing your communication according to the patient is really powerful.
And I know when I changed and pivoted into general practice, my trainer said, Louise, you're going to be a terrible GP because physicians in hospital are too robotic.
they'll never talk to patients properly.
I said, what do you mean, John?
I've always done really well.
He said, no, you're going to fail this exam.
You're going to be really bad.
And obviously when someone says you'll do bad, you do better,
which worked, of course.
But it's that ability of being able to ask the patient,
what's worrying you, which it seems really silly when at medical school,
of course, all you want to get is the diagnosis
and you want to make the best diagnosis at the quickest
compared to your peers.
But actually, the patients often aren't so bothered as the diagnosis.
it's more about how it's going to affect them and what does it mean.
And that's something that takes quite a long time, doesn't it, to realise, I think.
No, I think that's right.
And sometimes the diagnosis can be a gift.
We worry sometimes that patients will be really disappointed if you give them a name for their condition.
But in some ways it can be liberating because then a whole host of things might happen.
There might be a treatment option.
There might be information that they can access.
Yeah.
And it is interesting when I was in Manchester, and as you know, I wanted to do on
oncology, we had some amazing training with someone called Peter McGuire, who was a psychiatrist
who worked at the Christie Hospital. And this was many, many years ago. So it's quite unusual,
actually, where people didn't really talk about cancer then. And there was a lot of collusion going on.
And certainly when my dad had cancer in the 1970s, no one told him at all he had cancer, and it
just wasn't the done thing, which is, I know now, so wrong. So we had a lot of training about
breaking bad news and giving someone a cancer diagnosis. And I thought this is going to be awful.
so terrible but actually when you get it right people are so relieved actually if you say it in the
right way and prepare them in the right way and like you say then oh well that's why i've been
feeling this this is and then they can move on to the next step to try and decide where to go
what to do but it does take quite a lot of skill that's for sure we're all still learning
absolutely so you did all your neuroscience and you did your medicine and you've done gynecology
how much until we met did you know about the metaphors?
I'm putting you on the spot here, Dan.
Well, the truth is I've always been interested in hormones
and previous to now spending every waking hour
thinking about ways in which we can study the impact of hormones on lifelong health.
I spent 10 years at UCL working at the Institute for Women's Health there,
part of a team, really pioneering team,
looking at the impact of hormones on cancer.
So women's cancer, specifically womb cancer, but also ovarian cancer, breast cancer.
And one of the big learning points from that was that hormones are ungovernable.
They go everywhere.
They impact every body system.
They go to places where other chemicals and bioactive substances in the body don't go.
They cross the blood-brain barrier.
I don't think there's a body system that isn't impacted by hormones.
And so one of the interesting paradoxes, there are lots of paradoxes in this area.
One of the paradoxes is if you give contraception to women who are at risk of breast and ovarian cancer,
women, for example, with a BRCA mutation, fracobutation, you decrease their risk.
And we don't quite know why that is, but we think it might have something to do with avoiding the peaks and troughs of the menstrual cycle.
And that was really interesting to me.
Why is it that hormones sometimes are the bad guys and sometimes are the good guys?
Why is it that, for example, progesterone is considered a risk factor for breast cancer,
depends on quantity, depends on how it is given, but it's protective for womb cancer.
Those two cancers are hormone-driven, but there are contradictory effects of hormones.
So we give a small amount of progesterone, two women to protect their endometrium, the lining of the womb.
we don't want to give too much progesterone because then it can have an impact on the breast.
So women are much more complex than men in that regard.
And hormones are interesting, aren't they?
So they're just chemical messengers, really, aren't they, that just go in the bloodstream
and go to all our organs.
And we've got many, many different hormones in our bodies.
A lot of you will have heard of obviously insulin, thyroxin,
and then the ones that we always talk about are estrogen, progesterone, and testosterone as well,
actually, which mainly get produced from our ovaries when they're working when we're younger.
And, you know, our hormones, sex hormones, it's very interesting when you look back in time,
when the hormones were discovered, you know, when insulin was discovered, then it was associated
with the disease, diabetes.
When thyroxin was discovered, it was associated with a condition, hypothyroidism.
When estrogen was discovered, it was associated with symptoms, phasemotor symptoms and hot flushes.
which was such a shame actually, because if it had been associated with a condition,
we would be in a very different stage now.
And obviously they defined it as menopause, so stopping the menstrual cycle.
So the menopause has always been associated with periods, with fertility, with hot plushes.
And we, you know, you've been to conferences, I've been to many conferences,
and a lot of that conversation is about menstruation and razor motor symptoms.
Yet we know that our hormones go all over our body.
We know they affect everywhere.
But they also, like you say, they go through the blood-brain barrier.
So when you were learning and doing your amazing research,
looking at cognition and memory,
did you do anything about hormones then?
Well, the truth is neuroscientists, at least in my experience,
they always try to make things, the systems that they use to understand disease,
the models, as simple as possible.
and often they avoid actually using female rats and mice, for example, in experiments
because things that you can become a lot more complicated once you have an Easter cycle
and changes that are hormone-dependent.
So they sort of cut out all of that by just studying disease in male animals.
There are also ways in which you can manipulate cycles in experimental animals,
and certainly most experimental animals are not kept alive long enough to have a natural menopause,
and that's not a thing.
So I would say it's worse than not being on their radar.
They sort of actively cut out some of that variance
and some of that complexity
because they want to keep their confounding factors
as low as possible.
That's in some ways good in order to progress research.
It has the quite significant side effect
that our understanding is actually quite male-based
in certain areas in certain ways.
And also that we don't really study female-specific
physiology. And that's true for clinical medicine as well. Trials, for example, are commonly not
conducted with pregnant people in mind. That was a big problem in the COVID vaccination.
They just didn't know what to do with these people, kept having babies. And so this is a big
problem in how do you conduct and carry out research. So it wasn't really on the radar at all,
no, to answer your question. Well, it's been a problem for many decades, lack of research in women,
but lack of research in menopause as well. And certainly when you're
look at a lot of the studies, they look focusing on symptoms. And as many people listening,
know, I, of course, I'm interested in symptoms, but I'm more interested in the immune
modulating effects of our hormones and also the disease preventative effects of our hormones as
well, which has been neglected largely for many years. But the more work I do and the more
papers that I read, you know, I'm so interested in the brain. And I'm also interested
because I know how I felt when I didn't have hormones,
and it's the most crippling feeling ever to always, you know,
my brain is always active, I'm always thinking, I'm always trying to read,
I'm always, you know, I get up and I think, I'm in the shower and I think,
I use my brain a lot, and I felt like some zombie, you know,
this whole thing that people talk about the brain fog or the thinking through treacle,
and very hard to describe, you know, when people say my zest for life has got,
on and I'm just existing, I'm not living. And I don't know how you measure that in studies.
I just went with someone that just, you know, my 18-year-olds sometimes keeps texting me,
CBA can't be asked. And it's, you know, it is that sort of feeling where you just really,
everything is an effort. You know, I used to look at the pile of washing and think, that's probably
two loads of washing. I don't even want to put one load on. Now, actually, it takes a second.
I'm very lucky I have a washing machine. I can put it in and press the button and it doesn't
take long, but everything was overwhelming. And my memory was bad. My temper was awful. But all this
is brain. You know, obviously I was frustrated because I physically wasn't feeling as well,
especially having migraines and joint pains when I was perimenopausal. But it's,
without your brain, you're nothing. It's really difficult. And I see it and hear it time and time
again in the clinic of these poor women who say, I think I've got dementia. I can't remember the
words for that yellow thing that I'm eating that I see in the fruit bowl. And you say banana,
yes, of course it is. And it can be amusing, but it's really scary. But you talked at the
beginning about neurotransmitters. Just to explain what a neurotransmitter is, if you don't mind.
No, I'm happy to, but I wonder if it's worth taking a sort of a bit of a zoom out for a second
and just reflect on language before we go into neurotransmitters. Because you mentioned brain fog,
which I think is a bit of a, well, it's a term that we sort of hear a lot,
and it's often something that patients describe,
but in a way patients also describe,
we're given a sort of terminology often,
and we use it, and it's interesting to look at different cultures,
describe menopause transitions in different ways,
so spoken to people on the Indian subcontinent,
and often they go to their local doctors and talk about all of the body pain,
and that's a sort of cardinal feature.
if you look up to Benopause on the internet,
often hot flushes come up as a sort of a top thing.
But there was a study that came out before Christmas
by the Fawcett Society,
and it listed the most common symptoms in women,
and it was a large group of women,
4,000 people, I think,
4,000 women,
and it was a representative sample
with due concern to different ethnicities and, et cetera,
and it was called a panel survey.
So a really good study,
and what they found was that in the top 10,
in fact, the top five of,
symptoms were all brain-based. And that's really interesting to me because I think it's possible
that one of the reasons why this field is underfunded and under-researched and under-prioritized
and has been for so long is that it sort of happens in the corners. It is, you know, the gonadal bit,
the gonadal bit of the hypotivitory, hypothypithelamic pituitary gonadal axis. And so it happens sort of
down there in the ovaries, I guess, in the adrenals for testosterone. And actually to reconceive the
menopause as a cognitive disorder would answer both the kind of symptom portrait that patients
come with, they often talk about, describe, and sometimes the terminology we use isn't precise enough.
So people say brain, well, you know, why do we talk about brain fog in the menopause and why isn't
their proper nomenclature, a set of terms to be used?
You know, there's no reason why psychiatrists and general practitioners and gynecologists can't get
together and decide, well, this is a kind of hypoactive working memory state or actually begin
to describe it in scientific terms. Because once you name something, then you can study it,
then you can apply for funding for it. Then you see it everywhere. So I think that's one of the
myths that the menopause really happens down there in terms of hot flushes. Of course,
that's part of it. Sometimes symptoms that relate to genital urinary tract symptoms are very, very common
too, but the brain cognitive mood side of the menopause, I think, is not prioritized enough
and studied enough. And that's also one of the kind of exciting areas, and coming on to your
question about neurotransmitters. So I guess one way to attack that question, because it's a big
question, and I want to go into some detail, but I'm going to keep focused on the relevant
parts of neurophysiology. And I guess the thing to say is that there are, broadly speaking,
three or four or five neuromodulator systems.
So you've got your cholinergic.
So that's a lot of these symptoms happen all across the brain,
but especially maybe brain stem and basal part of the brain,
coninergic activity.
You've got your serotonergic, serotonin,
which is a predominant neurotransmitter in the amygdala,
and what we usually call the limbic system.
Again, also has brainwide effects.
Then you have the dopaminergic.
Dopamine is one of the major classes of families of neurotransmitters,
and that's obviously a big part of haphotlamic working memory reward,
also arousal and anticipation of reward.
It features predominantly in terms of dopamine,
and then Nordrenlin, which is, again, one of those big workhorses of the central nervous system.
And then there are others, glutamate, which I spent a lot of time working on in my research.
But all of these neurotransmitter systems operate across several different
huge highways of information across different brain areas.
But what's completely off the beaten path is the impact on all of those systems of estrogen and
testosterone.
And that's really, I think, one of the white patches on these maps, completely unexplored
territories.
And really, there is not just that it's not, you know, we can't find many papers,
there aren't many groups working on it.
If you speak to neuroscientists, they're sort of vaguely aware that estrogen
and androgens have neuromodulated effect on activation and metabolism and gray method density
and all these things, but they don't spend a lot of time studying it.
And I think one of the reasons, sadly, is because it happens in women, certainly estrogen.
And it's just, you know, at least traditionally, the community of brain researchers have been men.
So we can only hope that that will change by engaging with people, patients, coming together
and advocating and people like you putting the word out.
I think it is changing because as women we're realising more.
And, you know, sometimes it's not until you treat something, you see the response because,
as you know, with the perimenopause and menopause, there's no biochemical test.
And there's lots of reasons why our memory might not be as good as it was before.
And I know when I was struggling, my husband used to say, yeah, but Louise, you've just
got too much going on, you're working too hard.
You need to slow down and then your memory will be better.
And I said, but I just can't remember anything.
I really can't.
I'm really struggling.
And I'm so tired and what's going on.
And it was just because I remember once I was writing for the website that I launched,
and it was obviously menopause website.
Clearly didn't know I was perimenopausal.
And I remember my mum came into the study and she said, Louise,
will you stop working so hard?
And I said, but I'm really trying.
It's just taking me twice as long to do anything.
And it wasn't only when I replaced my hormones by being prescribed HR,
that then I thought, wow, that must be the effect.
And there's obviously a lot of talk are hormones, placebos.
Well, I don't think they are because we know that we've got receptors for cells in our brains that respond to estrogen and testosterone.
There's a reason that they're responding to hormones when we have them.
But like you say, it's so crucial that we can move this conversation forward with proper research, isn't it?
Yeah, I think it's a really exciting time, actually, because we've had sort of,
two decades now since the major studies came out and people got very afraid of hormones.
And that didn't only have the impact on prescription. So worldwide prescriptions dropped precipitously
in the mid to late 90s in many countries, certainly in the West, you know, 20, 30% of women
who needed it were on hormone replacement therapy and it dropped to zero in many places.
And we're sort of coming out of that two decades have lost time now.
But the other thing that we don't talk enough about is that that actually caused also a massive drop in funding for research.
And there's two decades of research that we need to catch up on too.
One of the exciting and fascinating areas that I don't think we talk enough about that are around the preventive effects of hormone therapy.
And so clearly many women are helped by hormone replacement when they're perimenopausal, postmenopausal.
but there's also significant effects on long-term cognition and preventive effects
in terms of avoiding or minimizing the effects of dementia in women who don't go through
and have years and years of low hormones in their 50s and 60s.
I did a small study on my local hospital recently of women who have had a new phorectomy,
so women who's had surgical removal of their ovaries,
if they were under the age of 45, did they have a conversation or any documentation
or any prescription of hormones and it was less than 10%.
And that's, you know, in many cases, you know, you go overnight essentially from having
your hormones to not having them.
So it's a sort of overnight menopause.
It will have huge symptomatic effects in those women in terms of mood and cognition
and a host of other things.
But the bigger worry for me, looking at that, is what is the effect of that?
long term in terms of the risk of Alzheimer's disease, Parkinson's disease.
And we know those risks are at least doubled.
And so that's an area where research and clinical practice really need to work together to find better answers.
Absolutely. And for those of you that haven't listened to the podcast I did with Walter Rocker talking about this,
with women who, especially when they're young, have their ovaries removed, how important is tears to consider hormones to reduce the risk of diseases.
It's worth having a listen. So there's a lot of work we need to do.
a lot of research. I'm very grateful for your time today, Dan, and I hope you'll be able to
come back and tell us some of the studies that you've been involved in going forward because
everyone, I'm sure, listening will agree that the need for proper research in perimenopause
and menopause and disease preventative effects, especially in the brain, is really overdue
and really needed. So before I finish, I'm not going to let you off the hook. There's three
take-home tips. So three reasons.
why the menopause should be thought of as more than just affecting our ovaries.
So what are the three things that you would, if you were talking to a stranger and telling them
about the menopause, what are the three things that you would say?
Well, I think the first thing I would say if I was a woman who either is contemplating
going through the perimenopause, menopause, woman in the midst of the perimenopoles,
which, by the way, it stretches out to seven years on average,
or if you're a woman who's menopause or having gone through to the other side,
I think don't accept the status quo of that how you're feeling is how it has to be.
I think what we need are women and men to advocate for choice,
for the ability to have the treatment not to accept that this is how it's going to be now.
my cognition is just reduced or my ability to function in my workplace is reduced.
And we have to guard against that sort of fatalistic mindset as a number one.
And number two that flows from that is speak to your doctor or your girlfriend or your
group of friends or your workplace to really become an advocate as a patient
because we need that external pressure, both as clinicians and as researchers.
And the third again flowing from that is if you are in a position to participate,
in research and to contribute.
We can't design studies or write up papers without the input from the women who are
facing this or have been helped by this.
And that voice is really important.
So, you know, this is a partnership and alliance, really, between doctors and researchers
and patients.
And that's 100% necessary in order to make progress in this area.
And progress we're definitely going to make.
Thank you ever so much for your time today, Dan.
I really appreciate it.
Pleasure.
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