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. 2020;74(4):1243-1252.
doi: 10.3233/JAD-191183.

Sex Differences in in vivo Alzheimer's Disease Neuropathology in Late Middle-Aged Hispanics

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Free PMC article

Sex Differences in in vivo Alzheimer's Disease Neuropathology in Late Middle-Aged Hispanics

José A Luchsinger et al. J Alzheimers Dis. 2020.
Free PMC article

Abstract

Background: Females may have a higher risk of dementia than males. It is not clear if sex differences in Alzheimer's disease (AD) neuropathology explain the higher risk of dementia in females. Sex differences in AD neuropathology might begin in middle age, decades before the sex differences in dementia are apparent.

Objective: To examine sex differences in in vivo AD neuropathology in late middle age.

Methods: We conducted a cross-sectional comparison of AD biomarkers among 266 Hispanic males and females (mean age: 64.0; 71.8% females) without dementia. Amyloid burden was measured as global standardized uptake value ratio (SUVR) with18F-Florbetaben positron emission tomography (PET). Neurodegeneration was ascertained as cortical thickness in AD signature areas using brain magnetic resonance imaging. Tau burden was measured as tau SUVR in the middle/inferior temporal gyri and medial temporal cortex with 18F-MK-6240 in 75 of the 266 participants.

Results: Females had higher amyloid SUVR and tau SUVR in the middle/inferior temporal gyri than males. However, females had higher cortical thickness than males and performed better in a test of verbal memory despite having higher AD neuropathology burden.

Conclusion: Higher amyloid and tau in females compared to males in late middle-age may explain the reported higher dementia risk in elderly females compared to males. Longitudinal follow-up is necessary to examine whether higher amyloid and tau burden in late middle age is followed by increased neurodegeneration and cognitive decline in females as compared with males.

Keywords: Amyloid; Hispanics; cognition; neurodegeneration; sex differences; tau.

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Conflict of interest statement

CONFLICT OF INTEREST/DISCLOSURES STATEMENT. JA Luchsinger receives a stipend from Wolters Kluwer, N.V. as Editor in Chief of the journal Alzheimer’s Disease and Associated Disorders, and has served as a paid consultant to vTv therapeutics, Inc. and Recruitment Partners. The other authors have no interests to declare.

Figures

Figure 1.
Figure 1.
Histograms showing the distribution of global brain amyloid standardized uptake volume ratio (SUVR). The top two histograms show the distribution for the entire sample with a dashed line (top-left) representing a normal density function with the mean and standard deviation of the full-sample amyloid SUVR. The solid line (top-right) represents a non-parametric kernel estimation. The bottom histograms stratify the sample by males (n = 75) and Females (n = 191) with separate normal (bottom-left) and kernel (bottom-right) for each sex.

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