Ontology highlight
ABSTRACT: Background
Aging and sex are major risk factors for developing late-onset Alzheimer's disease. Compared to men, women experience worse neuropathological burden and cognitive decline despite living longer with the disease. Similarly, male 3xTg-AD mice, developed to model Alzheimer's disease, no longer consistently exhibit standard Alzheimer's neuropathology yet experience higher rates of mortality - providing a unique opportunity to further elucidate this dichotomy. We hypothesized that sex differences in the biological aging process yield distinct pathological and molecular Alzheimer's disease signatures in males and females, which could be harnessed for therapeutic and biomarker development.Methods
We aged male and female, 3xTg-AD and B6129 control mice across their respec
SUBMITTER: Barber AJ
PROVIDER: S-EPMC11193202 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature