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January 14, 2026Biomedicine & Pharmacotherapy0 citationsOpen Access

Neuroendocrine signaling as a pathological seed for the female bias of Alzheimer’s disease and the concept of estrobolome

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DRDeepthi RapakaASArthur SaniotisMTMonkgogi Thatayaone

Key Points

  • To investigate the role of neuroendocrine factors and the gut microbiome in the female bias of Alzheimer's disease.
  • Review of existing literature on Alzheimer's disease prevalence and sex differences.
  • Analysis of the gut-estrogen-brain axis and its implications for neuroendocrine signaling.
  • Speculation on anatomical and neuroendocrinological factors affecting women's risk for Alzheimer's.
  • Estrogens and gut microbiota differences may influence Alzheimer's disease risk in women.
  • Oophorectomy before menopause is linked to an increased risk of Alzheimer's-related dementia.
  • Neuroendocrine signaling could act as a contributing factor in the pathophysiology of Alzheimer's.

Abstract

The prevalence of Alzheimer's disease (AD) is anticipated to escalate with the global increase in life expectancy. Although sex-based differences in AD have been previously documented, doubts persist regarding the relationship between sex and pathophysiological pathways. Sex hormones may contribute to these disparities, with a heightened risk of AD-related dementia associated with oophorectomy before menopause. We cannot ascertain if estrogens alone are solely accountable for this accelerated pathological progression of the disease. Estrogens are regulated by the gut microbiota. Thus, the gut-estrogen-brain axis appears to be implicated as a potential new influencer in the pathophysiology of AD, as the female microbiome differs from the male gut microbiome. This suggests it could be a risk factor for the higher prevalence of AD in women. This review speculates on the possible mechanisms for AD prevalence in women, including both anatomical and neuroendocrinological perspectives.

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Cite This Study

Rapaka et al. (2026) studied this question.

synapsesocial.com/papers/696719a60042a3ed5427d615https://doi.org/10.1016/j.biopha.2026.118999
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