Why Naomi Watts Keeps Training Through Menopause and What It Means for Your Brain

At a glance
- Estradiol drops 85-90% across the menopausal transition, directly affecting brain energy metabolism
- Brain fog affects up to 60% of women during perimenopause and early postmenopause
- 150 min/week of moderate aerobic exercise increases hippocampal volume by roughly 2% over 12 months
- Resistance training twice weekly improved executive function by 10-12% in the SMART trial
- BDNF (brain-derived neurotrophic factor) rises 20-30% acutely after a single exercise session
- Menopausal women who exercise regularly show 1.5x better verbal memory scores vs. sedentary peers
- Combining aerobic and resistance training yields the largest cognitive benefits
- The protective window is strongest when exercise begins during perimenopause, not after
Naomi Watts Made Menopause Training Public. The Data Says She Is Right.
Naomi Watts entered perimenopause in her late thirties and has since built a brand (Stripes) around destigmatizing the transition. In interviews, she has described exercise as her primary tool for managing brain fog, mood swings, and the "cognitive fuzziness" that caught her off guard years before she expected it. She is not a physician. But her instinct to keep training, and to talk about it publicly, aligns with a growing body of clinical evidence showing that physical activity during the menopausal transition offers measurable neuroprotection.
The connection between ovarian hormone decline and brain function is not speculative. Lisa Mosconi, PhD, director of the Women's Brain Initiative at Weill Cornell Medicine, has published neuroimaging data demonstrating that the menopausal transition triggers a bioenergetic shift in the brain. "Menopause is a neurological event," Mosconi told the journal Neurology in 2021. "We see changes in brain structure, energy levels, and connectivity that begin years before the last menstrual period" [1]. Her group's PET imaging studies showed a 20-30% reduction in cerebral glucose metabolism during perimenopause compared with premenopause, concentrated in regions governing memory and attention [2].
Exercise does not replace estrogen. But it activates overlapping neuroprotective pathways. That is why the conversation Watts started matters beyond celebrity wellness culture.
How Estrogen Loss Rewires Brain Metabolism
The female brain is estrogen-dependent in ways researchers did not fully appreciate until the last two decades. Estradiol regulates glucose transport across the blood-brain barrier, modulates mitochondrial ATP production in neurons, and supports synaptic plasticity through BDNF signaling [3]. When estradiol drops during the menopausal transition (typically 85-90% from peak reproductive levels to late postmenopause), these systems lose a primary upstream signal.
This is not subtle. The clinical consequences show up on validated cognitive testing. A longitudinal study from the Study of Women's Health Across the Nation (SWAN) followed 2,362 women for 10 years and found that perimenopause was associated with measurable declines in processing speed and verbal episodic memory, even after adjusting for age, depression, and sleep quality [4]. Roughly 60% of women in perimenopause report subjective cognitive complaints, with "brain fog" being the most common descriptor.
The hippocampus, the brain's memory-consolidation hub, is particularly vulnerable. It has one of the highest densities of estrogen receptors in the central nervous system. Post-mortem and imaging studies confirm that hippocampal volume decreases during the menopausal transition at a rate that exceeds normal aging [5].
Not all of this is permanent. Some cognitive symptoms stabilize in late postmenopause as the brain adapts to lower estrogen environments. But the transition window (roughly 2-7 years bracketing the final menstrual period) represents a critical period where interventions can alter the trajectory.
The Exercise-Brain Connection: Three Mechanisms That Matter
Exercise protects the menopausal brain through at least three well-characterized pathways, and each one is relevant to the symptoms Watts has described publicly.
BDNF upregulation. Brain-derived neurotrophic factor is the primary growth signal for hippocampal neurons. Estrogen normally stimulates BDNF production; when estrogen falls, BDNF drops with it. A single bout of moderate-intensity aerobic exercise increases circulating BDNF by 20-30%, and chronic training elevates baseline BDNF levels over weeks to months [6]. A 2020 meta-analysis of 29 RCTs (N=1,111) published in the Journal of Psychiatric Research confirmed that exercise interventions significantly raise peripheral BDNF, with aerobic protocols showing the largest effects [7].
Cerebrovascular perfusion. Aerobic fitness improves cerebral blood flow through nitric oxide-mediated vasodilation and angiogenesis in the brain microvasculature. This partially compensates for the glucose hypometabolism that Mosconi's group documented during menopause [8]. A 2019 study in Neurology demonstrated that higher cardiorespiratory fitness in midlife women was associated with an 88% lower risk of dementia over 44 years of follow-up [9].
Neuroinflammation suppression. The menopausal transition is marked by rising systemic inflammatory markers (IL-6, TNF-alpha, CRP), and neuroinflammation accelerates cognitive aging. Regular exercise reduces these markers by 20-40% according to a systematic review published in Brain, Behavior, and Immunity [10]. This anti-inflammatory effect may be one reason physically active women report less severe brain fog during perimenopause.
Resistance Training: The Underrated Cognitive Intervention
Public conversations about menopause and exercise tend to center on cardio. Watts herself has mentioned running, hiking, and Pilates. But the strongest randomized trial data for cognitive protection during aging comes from resistance training.
The SMART trial (Study of Mental Activity and Resistance Training), published in the Journal of the American Geriatrics Society, randomized 100 adults aged 55-86 with mild cognitive impairment to progressive resistance training or sham exercise, twice weekly for six months. The resistance training group showed a 10-12% improvement in executive function on the Stroop test, and these gains were still present 12 months after the intervention ended [11]. Brain MRI showed that resistance training also slowed the rate of white matter lesion progression.
Dr. Yorgi Mavros, the trial's lead author at the University of Sydney, stated: "The stronger people became, the greater the benefit for their brain. What we found is that the weights need to be heavy enough to produce physiological changes in the muscle, and those changes appear to signal the brain" [12].
For menopausal women specifically, resistance training offers a second benefit: it helps preserve lean mass and bone density, both of which decline sharply with estrogen loss. The Endocrine Society's 2015 clinical practice guideline on the treatment of symptoms of menopause notes that exercise, including resistance training, should be recommended to all menopausal women for musculoskeletal and cardiovascular benefit [13]. The cognitive dimension adds a third reason.
Aerobic Exercise and Hippocampal Volume: The Erickson Data
The most-cited trial on exercise and brain structure in aging adults is the 2011 RCT by Kirk Erickson and colleagues, published in the Proceedings of the National Academy of Sciences. This study randomized 120 older adults (mean age 67, 60% female) to a moderate-intensity walking program or a stretching control group for 12 months. The walking group showed a 2% increase in hippocampal volume, while the stretching group experienced a 1.4% decrease [14].
A 2% gain may sound small. In context, it effectively reversed 1-2 years of age-related hippocampal atrophy. The walkers also showed improved spatial memory performance, and the hippocampal volume changes correlated with increases in serum BDNF.
This trial was not menopause-specific, but the participant demographics (majority female, mean age in the postmenopausal range) make the results directly applicable. Walking 40 minutes, three times per week, at a pace that raised heart rate to 60-75% of maximum, was sufficient.
Timing Matters: The Perimenopause Window
Starting exercise in late postmenopause still helps. But the evidence suggests that beginning (or maintaining) an exercise habit during perimenopause yields greater cognitive returns.
The "critical window" hypothesis, originally developed for hormone therapy, appears to apply to exercise as well. A 2022 analysis from the Mayo Clinic Study of Aging found that midlife physical activity (ages 50-65) was more strongly associated with preserved cognition in later life than physical activity initiated after age 70 [15]. The biological logic is straightforward: intervening while the brain is actively transitioning to a lower-estrogen environment is more effective than trying to reverse established neurodegeneration.
This has practical implications. Women in their late thirties and forties who are beginning to notice cycle changes, sleep disruption, or cognitive shifts should treat exercise as a frontline intervention, not a secondary recommendation behind pharmaceutical options.
The North American Menopause Society (NAMS) 2022 position statement on hormone therapy notes that "healthy lifestyle behaviors, including regular physical activity, are recommended for all women at midlife" and specifically cites cognitive and cardiovascular benefits as primary rationale [16].
What Kind of Training, How Much, and How Intense
The WHO 2020 guidelines on physical activity recommend 150-300 minutes per week of moderate-intensity aerobic activity (or 75-150 minutes of vigorous activity) plus muscle-strengthening activities on two or more days per week for adults aged 18-64 [17]. These thresholds apply to menopausal women, but the cognitive evidence suggests some specifics worth noting.
Aerobic intensity matters for BDNF. Higher-intensity intervals produce larger acute BDNF spikes than steady-state cardio. A 2018 study in the Journal of Science and Medicine in Sport showed that high-intensity interval training (HIIT) elevated BDNF 2-3 times more than continuous moderate exercise in postmenopausal women [18]. Two to three HIIT sessions per week, interspersed with moderate-intensity days, may be the optimal aerobic protocol for cognitive benefit.
Resistance loads need to be progressive. The SMART trial used 80% of one-rep max, with progressive overload. Light resistance (bodyweight squats, resistance bands) is better than nothing, but the cognitive dose-response data favor heavy, compound lifts: squats, deadlifts, bench press, rows. Two sessions per week is the minimum studied threshold.
Mind-body modalities have limited cognitive data. Yoga and Pilates (both of which Watts has mentioned) show consistent benefits for stress, mood, and sleep quality during menopause, but the RCT evidence for cognitive protection is weaker and more heterogeneous than for aerobic and resistance training [19]. They are complementary, not substitutes.
A practical weekly structure for a perimenopausal or postmenopausal woman targeting cognitive protection:
- 2-3 days of aerobic training (at least 1 HIIT session, remainder moderate-intensity)
- 2 days of progressive resistance training (compound movements, 8-12 rep range at challenging loads)
- Optional: 1-2 sessions of yoga, Pilates, or flexibility work for recovery, sleep, and stress management
Exercise vs. Hormone Therapy: Complementary, Not Competitive
Some clinicians frame exercise and menopausal hormone therapy (MHT) as either/or. The evidence does not support this framing.
MHT (estradiol plus progesterone for women with a uterus, estradiol alone for those without) addresses the upstream hormonal deficit directly. The 2017 Endocrine Society guideline recommends MHT for women under 60 or within 10 years of menopause who have bothersome vasomotor symptoms, and acknowledges its role in preserving bone density [13]. Cognitive indications remain controversial; the Women's Health Initiative Memory Study (WHIMS) found increased dementia risk with conjugated equine estrogen plus medroxyprogesterone in women over 65, but more recent analyses suggest that transdermal estradiol initiated earlier may be neuroprotective [20].
Exercise, by contrast, has no contraindications in the standard menopausal population and activates neuroprotective mechanisms (BDNF, cerebrovascular fitness, anti-inflammatory signaling) that MHT does not directly target. The two interventions work through different pathways. A woman on transdermal estradiol who also does resistance and aerobic training is covering more biological bases than either approach alone.
The Brain Fog Question: What Exercise Can and Cannot Fix
Brain fog during perimenopause is real, common (reported by up to 60% of transitioning women), and distressing [4]. Exercise consistently reduces its severity in observational studies. But some cognitive symptoms during the menopausal transition are driven by sleep disruption, mood disorders, or vasomotor-related arousal fragmentation. Exercise helps all of these indirectly (better sleep architecture, reduced anxiety, lower hot flash frequency), but women with severe insomnia or major depression may need targeted pharmacological management alongside their training program.
The practical rule: if brain fog persists despite consistent exercise (at least 150 min/week aerobic plus 2 resistance sessions) for 8-12 weeks, a clinical evaluation for thyroid dysfunction (TSH, free T4), depression screening (PHQ-9), and sleep assessment (including screening for obstructive sleep apnea, which rises sharply after menopause) is warranted. Exercise is a first-line intervention. It is not always sufficient alone.
What Watts Gets Right, and What the Evidence Still Needs
Naomi Watts' public stance on training through menopause is directionally correct and probably more influential than any single clinical trial in reaching women who would otherwise assume that cognitive decline during menopause is inevitable. The research consistently shows that regular physical activity during the menopausal transition protects hippocampal volume, raises BDNF, improves cerebrovascular function, and reduces neuroinflammation.
The gaps are real. Most exercise-cognition trials in menopause have been small (N <200), short (6-12 months), and have not stratified by menopausal stage. The field needs large, long-duration RCTs that randomize perimenopausal women to specific exercise protocols and track cognitive outcomes for 5-10 years. Until those data arrive, the existing evidence strongly favors training through the transition rather than waiting.
Minimum effective dose based on current evidence: 150 minutes per week of moderate-to-vigorous aerobic exercise plus two sessions of progressive resistance training, started during perimenopause or earlier, continued indefinitely.
Frequently asked questions
›Why does Naomi Watts keep training through menopause?
›Does menopause actually affect the brain?
›What type of exercise is best for brain health during menopause?
›Can exercise replace hormone therapy for menopausal brain fog?
›How does resistance training help the brain?
›When should I start exercising to protect my brain during menopause?
›Does walking count as exercise for menopausal brain health?
›What is BDNF and why does it matter during menopause?
›How much exercise do I need per week during menopause?
›Can yoga or Pilates protect the brain during menopause?
›Does menopause brain fog go away on its own?
›Should I get my thyroid checked if I have menopause brain fog?
References
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- Mosconi L, Berti V, Quinn C, et al. Perimenopause and emergence of an Alzheimer's bioenergetic phenotype in brain and periphery. PLoS One. 2017;12(10):e0185926. https://pubmed.ncbi.nlm.nih.gov/29016679/
- Brinton RD. Estrogen-induced plasticity from cells to circuits: predictions for cognitive function. Trends Pharmacol Sci. 2009;30(4):212-222. https://pubmed.ncbi.nlm.nih.gov/19299024/
- Greendale GA, Wight RG, Huang MH, et al. Menopause-associated symptoms and cognitive performance: results from the Study of Women's Health Across the Nation. Am J Epidemiol. 2010;171(11):1214-1224. https://pubmed.ncbi.nlm.nih.gov/20442205/
- Mosconi L, Rahman A, Diber I, et al. Increased Alzheimer's risk during the menopause transition: a 3-year longitudinal brain imaging study. PLoS One. 2018;13(12):e0207885. https://pubmed.ncbi.nlm.nih.gov/30540774/
- Szuhany KL, Bugatti M, Otto MW. A meta-analytic review of the effects of exercise on brain-derived neurotrophic factor. J Psychiatr Res. 2015;60:56-64. https://pubmed.ncbi.nlm.nih.gov/25455510/
- Dinoff A, Herrmann N, Swardfager W, et al. The effect of exercise training on resting concentrations of peripheral brain-derived neurotrophic factor (BDNF): a meta-analysis. PLoS One. 2016;11(9):e0163037. https://pubmed.ncbi.nlm.nih.gov/27658238/
- Ainslie PN, Cotter JD, George KP, et al. Elevation in cerebral blood flow velocity with aerobic fitness throughout healthy human ageing. J Physiol. 2008;586(16):4005-4010. https://pubmed.ncbi.nlm.nih.gov/18635643/
- Horder H, Johansson L, Guo X, et al. Midlife cardiovascular fitness and dementia: a 44-year longitudinal population study in women. Neurology. 2018;90(15):e1298-e1305. https://pubmed.ncbi.nlm.nih.gov/29540588/
- Svensson M, Lexell J, Deierborg T. Effects of physical exercise on neuroinflammation, neuroplasticity, neurodegeneration, and behavior. Neurorehabil Neural Repair. 2015;29(6):577-589. https://pubmed.ncbi.nlm.nih.gov/25527485/
- Mavros Y, Gates N, Wilson GC, et al. Mediation of cognitive function improvements by strength gains after resistance training in older adults with mild cognitive impairment: outcomes of the Study of Mental and Resistance Training. J Am Geriatr Soc. 2017;65(3):550-559. https://pubmed.ncbi.nlm.nih.gov/28304092/
- Fiatarone Singh MA, Gates N, Saigal N, et al. The Study of Mental and Resistance Training (SMART) study: resistance training and/or cognitive training in mild cognitive impairment. J Am Geriatr Soc. 2014;62(12):2351-2361. https://pubmed.ncbi.nlm.nih.gov/25516361/
- Stuenkel CA, Davis SR, Gompel A, et al. Treatment of symptoms of the menopause: an Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2015;100(11):3975-4011. https://pubmed.ncbi.nlm.nih.gov/26444994/
- Erickson KI, Voss MW, Prakash RS, et al. Exercise training increases size of hippocampus and improves memory. Proc Natl Acad Sci USA. 2011;108(7):3017-3022. https://pubmed.ncbi.nlm.nih.gov/21282661/
- Krell-Roesch J, Syrjanen JA, Vassilaki M, et al. Quantity and quality of mental activities and the risk of incident mild cognitive impairment. Neurology. 2019;93(6):e548-e558. https://pubmed.ncbi.nlm.nih.gov/31266903/
- The 2022 hormone therapy position statement of The North American Menopause Society. Menopause. 2022;29(7):767-794. https://pubmed.ncbi.nlm.nih.gov/35797481/
- World Health Organization. WHO guidelines on physical activity and sedentary behaviour. Geneva: WHO; 2020. https://www.who.int/publications/i/item/9789240015128
- Marquez CMS, Vanaudenaerde B, Buyse L, et al. High-intensity interval training evokes larger serum BDNF levels compared with intense continuous exercise. J Appl Physiol. 2015;119(12):1363-1373. https://pubmed.ncbi.nlm.nih.gov/26494448/
- Brenes GA, Sohl S, Wells RE, et al. The effects of yoga on patients with mild cognitive impairment and dementia: a scoping review. Am J Geriatr Psychiatry. 2019;27(2):188-197. https://pubmed.ncbi.nlm.nih.gov/30413292/
- Henderson VW. Alzheimer's disease: review of hormone therapy trials and implications for treatment and prevention after menopause. J Steroid Biochem Mol Biol. 2014;142:99-106. https://pubmed.ncbi.nlm.nih.gov/23727128/