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GWAS Study

A genome-wide association study of aging.

Walter S, Atzmon G, Demerath EW et al.

21782286 PubMed ID
GWAS Study Type
35418 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WS
Walter S
AG
Atzmon G
DE
Demerath EW
GM
Garcia ME
KR
Kaplan RC
KM
Kumari M
LK
Lunetta KL
MY
Milaneschi Y
TT
Tanaka T
TG
Tranah GJ
VU
Völker U
YL
Yu L
AA
Arnold A
BE
Benjamin EJ
BR
Biffar R
BA
Buchman AS
BE
Boerwinkle E
CD
Couper D
DJ
De Jager PL
ED
Evans DA
HT
Harris TB
HW
Hoffmann W
HA
Hofman A
KD
Karasik D
KD
Kiel DP
KT
Kocher T
KM
Kuningas M
LL
Launer LJ
LK
Lohman KK
LP
Lutsey PL
MJ
Mackenbach J
MK
Marciante K
PB
Psaty BM
RE
Reiman EM
RJ
Rotter JI
SS
Seshadri S
SM
Shardell MD
SA
Smith AV
VD
van Duijn C
WJ
Walston J
ZM
Zillikens MC
BS
Bandinelli S
BS
Baumeister SE
BD
Bennett DA
FL
Ferrucci L
GV
Gudnason V
KM
Kivimaki M
LY
Liu Y
MJ
Murabito JM
NA
Newman AB
TH
Tiemeier H
FN
Franceschini N
Chapter II

Abstract

Summary of the research findings

Human longevity and healthy aging show moderate heritability (20%-50%). We conducted a meta-analysis of genome-wide association studies from 9 studies from the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium for 2 outcomes: (1) all-cause mortality, and (2) survival free of major disease or death. No single nucleotide polymorphism (SNP) was a genome-wide significant predictor of either outcome (p < 5 × 10(-8)). We found 14 independent SNPs that predicted risk of death, and 8 SNPs that predicted event-free survival (p < 10(-5)). These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease. In addition to considerable overlap between the traits, pathway and network analysis corroborated these findings. These findings indicate that variation in genes involved in neurological processes may be an important factor in regulating aging free of major disease and achieving longevity.

25,007 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

35418
Total Participants
GWAS
Study Type
Yes
Replicated
10,411 European ancestry individuals
Replication Participants
European
Ancestry
U.S., U.K., Italy, Netherlands, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.