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GWAS Study

Identification of genetic heterogeneity of Alzheimer's disease across age.

Lo MT, Kauppi K, Fan CC et al.

30979435 PubMed ID
GWAS Study Type
6559 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Lo MT
KK
Kauppi K
FC
Fan CC
SN
Sanyal N
RE
Reas ET
SV
Sundar VS
LW
Lee WC
DR
Desikan RS
ML
McEvoy LK
CC
Chen CH
Chapter II

Abstract

Summary of the research findings

The risk of APOE for Alzheimer's disease (AD) is modified by age. Beyond APOE, the polygenic architecture may also be heterogeneous across age. We aim to investigate age-related genetic heterogeneity of AD and identify genomic loci with differential effects across age. Stratified gene-based genome-wide association studies and polygenic variation analyses were performed in the younger (60-79 years, N = 14,895) and older (≥80 years, N = 6559) age-at-onset groups using Alzheimer's Disease Genetics Consortium data. We showed a moderate genetic correlation (rg = 0.64) between the two age groups, supporting genetic heterogeneity. Heritability explained by variants on chromosome 19 (harboring APOE) was significantly larger in younger than in older onset group (p < 0.05). APOE region, BIN1, OR2S2, MS4A4E, and PICALM were identified at the gene-based genome-wide significance (p < 2.73 × 10-6) with larger effects at younger age (except MS4A4E). For the novel gene OR2S2, we further performed leave-one-out analyses, which showed consistent effects across subsamples. Our results suggest using genetically more homogeneous individuals may help detect additional susceptible loci.

2,399 European ancestry cases, 4,160 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6559
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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