학술논문

Polygenic resilience scores capture protective genetic effects for Alzheimer’s disease
Document Type
article
Source
Translational Psychiatry. 12(1)
Subject
Genetics
Alzheimer's Disease
Brain Disorders
Human Genome
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Genetic Testing
Neurodegenerative
Prevention
Dementia
Aging
Acquired Cognitive Impairment
Aetiology
2.1 Biological and endogenous factors
Alzheimer Disease
Apolipoprotein E4
Apolipoproteins E
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Multifactorial Inheritance
Risk Factors
Alzheimer’s Disease Neuroimaging Initiative
Clinical Sciences
Public Health and Health Services
Psychology
Language
Abstract
Polygenic risk scores (PRSs) can boost risk prediction in late-onset Alzheimer's disease (LOAD) beyond apolipoprotein E (APOE) but have not been leveraged to identify genetic resilience factors. Here, we sought to identify resilience-conferring common genetic variants in (1) unaffected individuals having high PRSs for LOAD, and (2) unaffected APOE-ε4 carriers also having high PRSs for LOAD. We used genome-wide association study (GWAS) to contrast "resilient" unaffected individuals at the highest genetic risk for LOAD with LOAD cases at comparable risk. From GWAS results, we constructed polygenic resilience scores to aggregate the addictive contributions of risk-orthogonal common variants that promote resilience to LOAD. Replication of resilience scores was undertaken in eight independent studies. We successfully replicated two polygenic resilience scores that reduce genetic risk penetrance for LOAD. We also showed that polygenic resilience scores positively correlate with polygenic risk scores in unaffected individuals, perhaps aiding in staving off disease. Our findings align with the hypothesis that a combination of risk-independent common variants mediates resilience to LOAD by moderating genetic disease risk.