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Menopause Status Moderates Sex Differences in Tau Burden: A Framingham PET Study
- Source :
- Annals of Neurology, 92(1), 11-22. Wiley
- Publication Year :
- 2022
-
Abstract
- OBJECTIVE: Women have a higher lifetime risk of AD than men. Among cognitively normal (CN) older adults, women exhibit elevated tau positron emission tomography (PET) signal compared with men. We explored whether menopause exacerbates sex differences in tau deposition in middle-aged adults.METHODS: 328 CN participants from the Framingham Study (mean age=57yrs(±10yrs), 161 women, of whom, 104 were post-menopausal) underwent tau and β-amyloid (Aβ)-PET neuroimaging. We examined global Aβ-PET, and tau-PET signal in five regions identified a priori as demonstrating significant sex differences in older adults (in temporal, inferior parietal, middle frontal, and lateral occipital regions). We examined sex and menopause status-related differences in each region-of-interest, using linear regressions, as well as interactions with Aβ and APOEε4 genotype.RESULTS: Women exhibited higher tau-PET signal (pINTERPRETATION: Clear divergence in tauopathy between the sexes are apparent approximately 20 years earlier than previously reported. Menopause status moderated sex differences in Aβ and tau-PET burden, with tau first appearing post-menopause. Sex and menopause differences consistently appeared in middle frontal and parieto-occipital regions but were not moderated by Aβ burden or APOEε4, suggesting that menopause-related tau vulnerability may be independent of AD-related pathways. This article is protected by copyright. All rights reserved.
- Subjects :
- RISK
Male
Sex Characteristics
Amyloid beta-Peptides
DEMENTIA
APOLIPOPROTEIN-E GENOTYPE
tau Proteins
ASSOCIATION
Middle Aged
COGNITIVE IMPAIRMENT
PREVALENCE
PATHOLOGY
AGE
Neurology
Alzheimer Disease
Positron-Emission Tomography
Humans
NATURAL MENOPAUSE
Cognitive Dysfunction
Female
Neurology (clinical)
Menopause
ALZHEIMER-DISEASE
Aged
Subjects
Details
- ISSN :
- 15318249 and 03645134
- Volume :
- 92
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Annals of neurology
- Accession number :
- edsair.doi.dedup.....114818bf83961d9be32675eb7fdd5017