Genetic Prοpensity for Different Aspects of Dementia Pathology and Cognitive Decline in a Community Elderly Population
Stefanos N. Sampatakakis, Niki Mourtzi, Alex Hatzimanolis, Georgios Koutsis, Sokratis Charisis, Iliana Gkelmpesi, Eirini Mamalaki, Eva Ntanasi, Alfredo Ramirez, Mary Yannakoulia, Mary H. Kosmidis, Efthimios Dardiotis, Georgios Hadjigeorgiou, Paraskevi Sakka, Nikolaos Scarmeas

TL;DR
This study explores how genetic factors linked to dementia pathology are associated with cognitive decline in older adults.
Contribution
The study reveals that genetic predisposition to amyloid-beta and white matter hyperintensities affects global and memory-specific cognitive decline differently across subgroups.
Findings
Higher PRS for Aβ42 and WMH were associated with faster global cognitive decline.
The effect of PRS on memory decline varied by age, sex, and education level.
Genetic associations with global decline were consistent across subgroups.
Abstract
In the present study, we investigated the association of genetic predisposition with specific dimensions of dementia pathophysiology for global and domain-specific cognitive decline in older adults. The sample was drawn from the Hellenic Longitudinal Investigation of Aging and Diet (HELIAD) study, comprising 512 cognitively normal individuals over 64 years of age, with a mean follow-up of 2.9 years. Cognitive function was evaluated through a neuropsychological test battery, while genetic predisposition was assessed based on two distinct Polygenic Risk Scores (PRS) for amyloid-beta 42 (Aβ42) and white matter hyperintensities (WMH). The association of each PRS with the cognitive decline rate was examined using generalized estimating equation models. In the whole sample, higher PRSs Aβ42 (β = −0.042) and WMH (β =−0.029) were associated with a higher rate of global cognitive decline per…
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Taxonomy
TopicsDementia and Cognitive Impairment Research · Folate and B Vitamins Research · Alzheimer's disease research and treatments
