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Menopause Status Moderates Sex Differences in Tau Burden: A Framingham PET Study

Authors :
Rachel F. Buckley
Adrienne O'Donnell
Emer R. McGrath
Heidi I.L. Jacobs
Cristina Lois
Claudia L. Satizabal
Saptaparni Ghosh
Zoe B. Rubinstein
Joanne M. Murabito
Reisa A. Sperling
Keith A. Johnson
Sudha Seshadri
Alexandra S. Beiser
RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience
Psychiatrie & Neuropsychologie
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.

Details

ISSN :
15318249 and 03645134
Volume :
92
Issue :
1
Database :
OpenAIRE
Journal :
Annals of neurology
Accession number :
edsair.doi.dedup.....114818bf83961d9be32675eb7fdd5017