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GWAS Study

Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease.

Wang H, Yang J, Schneider JA et al.

32450446 PubMed ID
GWAS Study Type
1316 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WH
Wang H
YJ
Yang J
SJ
Schneider JA
DJ
De Jager PL
BD
Bennett DA
ZH
Zhang HY
Chapter II

Abstract

Summary of the research findings

Genome-wide association studies have identified many loci associated with Alzheimer's dementia. However, these variants only explain part of the heritability of Alzheimer's disease (AD). As genetic epistasis can be a major contributor to the "missing heritability" of AD, we conducted genome-wide epistasis screening for AD pathologies in 2 independent cohorts. First, we performed a genome-wide epistasis study of AD-related brain pathologies (Nmax = 1318) in ROS/MAP. Candidate interactions were validated using cerebrospinal fluid biomarkers of AD in ADNI (Nmax = 1128). Further functional analysis tested the association of candidate interactions with neuroimaging phenotypes. For tau and amyloid-β pathology, we identified 2803 and 464 candidate SNP-SNP interactions, respectively. Associations of candidate SNP-SNP interactions with brain volume and white matter changes from neuroimages provides additional insights into their molecular functions. Transcriptional analysis supported possible gene-gene interactions identified by statistical screening through their co-expression in the brain. In summary, we outlined an exhaustive epistasis analysis to identify novel genetic interactions with potential roles in AD pathologies. We further delved into the functional relevance of candidate interactions by association with neuroimaging phenotypes and analysis of co-expression between corresponding gene pairs.

1,316 individuals

Chapter III

Study Statistics

Key metrics and study information

1316
Total Participants
GWAS
Study Type
No
Replicated
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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