Midlife brain vulnerability: Sex differences in functional magnetic resonance imaging and Alzheimer's disease risk

Midlife marks a critical period for detecting Alzheimer's disease (AD) risk because biological and lifestyle factors exceedingly influence brain aging. Konishi et al. used functional magnetic resonance imaging to examine sex differences and risk factors (apolipoprotein E <i>(APOE)</i> ε4, hypertension, type 2 diabetes, depression) on memory-related brain activity starting in midlife. High-risk women showed greater hippocampal hyperactivity, amyloid-β accumulation, and memory deficits than other groups. However, limited sample diversity, lack of tau imaging, unmeasured hormonal levels, and vascular influences constrain interpretations. These findings emphasize the need for sex-informed, mechanistically precise approaches in AD research targeting preclinical stages of disease progression.

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Publication Details

Journal
Journal of Alzheimer s Disease
Published
2025-11-05
DOI
https://doi.org/10.1177/13872877251392238
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
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article

Midlife brain vulnerability: Sex differences in functional magnetic resonance imaging and Alzheimer's disease risk

Ian M. McDonough, Alin Alshaheri Durazo
Journal of Alzheimer s Disease
Dementia and Cognitive Impairment Research
article

Midlife brain vulnerability: Sex differences in functional magnetic resonance imaging and Alzheimer's disease risk

Ian M. McDonough, Alin Alshaheri Durazo
article en

Abstract

Midlife marks a critical period for detecting Alzheimer's disease (AD) risk because biological and lifestyle factors exceedingly influence brain aging. Konishi et al. used functional magnetic resonance imaging to examine sex differences and risk factors (apolipoprotein E <i>(APOE)</i> ε4, hypertension, type 2 diabetes, depression) on memory-related brain activity starting in midlife. High-risk women showed greater hippocampal hyperactivity, amyloid-β accumulation, and memory deficits than other groups. However, limited sample diversity, lack of tau imaging, unmeasured hormonal levels, and vascular influences constrain interpretations. These findings emphasize the need for sex-informed, mechanistically precise approaches in AD research targeting preclinical stages of disease progression.

Journal of Alzheimer s DiseaseVol. 109(1)
Binghamton University (US)
Openalex Percentile: Top 61%
Dementia and Cognitive Impairment Research
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