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Neurology· 2026Q1

Reproductive Lifespan and Hormonal Therapy in Relation to Later-Life Neurovascular Health in Community-Dwelling Older Women

Giulia Lorenzon, Gemma García‐Lluch, Gillian Coughlan, Shireen Sindi et al.

Short summary

Longer reproductive lifespan (OR=0.90) and menopausal hormone therapy (MHT) use (OR=0.43) were associated with lower cerebral small vessel disease (SVD) burden in 70-year-old women. Oral contraceptives (OC) and MHT use were linked to greater white matter integrity, with combined use showing the highest fractional anisotropy (OR=0.45).

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Key points

  • Longer reproductive span (menarche to menopause) was associated with 10% lower odds of SVD burden (OR=0.90).
  • Menopausal hormone therapy (MHT) use was linked to 57% lower odds of SVD burden (OR=0.43).
  • Combined oral contraceptive (OC) and MHT use was associated with the highest white matter integrity (fractional anisotropy, OR=0.45).
  • MHT use was associated with greater cortical thickness in AD-vulnerable areas among APOE-ε4 carriers (β=0.38).

AI-generated from the title and abstract; the full text is not read.

Abstract

ABSTRACT Background Women face greater vulnerability to dementia and Alzheimer’s disease (AD), potentially due to estrogen fluctuations across the lifespan. However, its role in vascular brain health is unclear. We investigated associations between lifelong estrogen exposure—endogenous (reproductive span) and exogenous (oral contraceptives [OC], menopausal hormone therapy [MHT])—and late-life vascular brain injury, AD-related atrophy, and APOE -ε4 modification. Methods and findings We included 352 cognitively unimpaired 70-years-old women from the Gothenburg H70-1944 Birth Cohort with brain MRI and 5-year follow-up. Reproductive lifespan was calculated as age at menopause or oophorectomy minus age at menarche. OC and MHT use were self-reported. Outcomes included cerebral small vessel disease (SVD), AD-related cortical thickness, and white-matter integrity (fractional anisotropy). Linear and multinomial regression and mixed-effects models were adjusted for confounders and stratified by APOE -ε4. Longer reproductive span (OR=0.90 [95%CI 0.83–0.98]) and MHT use (OR=0.43 [95% CI 0.20–0.92]) were linked to lower SVD burden, particularly fewer perivascular spaces and microbleeds. OC and MHT were associated with greater white matter integrity, with additive use throughout life showing the highest fractional anisotropy (OR=0.45 [95% CI 0.12–0.78]). MHT use was associated with greater thickness in areas often affected in AD among APOE -ε4 carriers (β=0.38 [95% CI 0.01–0.76]) but not in non-carriers. Longer estrogen exposure was linked to stable cortical thickness and WMH trajectories over time. Conclusions Extended estrogen exposure throughout life—both endogenous and exogenous—appear to support late-life cerebrovascular health in women, with potential genotype-specific neuroprotective effects. Given the current absence of sex-specific prevention guidelines for cognitive disorders, future research should clarify estrogen’s long-term impact on brain health and cognition to inform personalized medicine.

The authors' abstract, as published at the source. Neurology, 2026 · DOI ↗

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Field: Endocrinology, Diabetes and Metabolism

Endocrinology, Diabetes and MetabolismMedicine