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

TitleSex Differences in in vivo Alzheimer's Disease Neuropathology in Late Middle-Aged Hispanics.
Publication TypeJournal Article
Year of Publication2020
AuthorsLuchsinger JA, Palta P, Rippon B, Soto L, Ceballos F, Pardo M, Laing K, Igwe K, Johnson A, Tomljanovic Z, He H, Reitz C, Kreisl W, Razlighi Q, Teresi J, Moreno H, Brickman AM
JournalJ Alzheimers Dis
Volume74
Issue4
Pagination1243-1252
Date Published2020
ISSN1875-8908
KeywordsAlzheimer Disease, Amyloidogenic Proteins, Biomarkers, Brain, Cross-Sectional Studies, Female, Hispanic or Latino, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuroimaging, Positron-Emission Tomography, Sex Factors, tau Proteins
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.

DOI10.3233/JAD-191183
Alternate JournalJ Alzheimers Dis
PubMed ID32250303
PubMed Central IDPMC7656318
Grant ListR01 AG050440 / AG / NIA NIH HHS / United States
P50 AG008702 / AG / NIA NIH HHS / United States
P30 AG059303 / AG / NIA NIH HHS / United States
P30 AG066462 / AG / NIA NIH HHS / United States
RF1 AG051556 / AG / NIA NIH HHS / United States
UL1 TR001873 / TR / NCATS NIH HHS / United States
K24 AG045334 / AG / NIA NIH HHS / United States
R00 AG052830 / AG / NIA NIH HHS / United States
Related Institute: 
Brain Health Imaging Institute (BHII)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065