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GWAS Study

Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.

Timmers PR, Mounier N, Lall K et al.

30642433 PubMed ID
GWAS Study Type
500193 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TP
Timmers PR
MN
Mounier N
LK
Lall K
FK
Fischer K
NZ
Ning Z
FX
Feng X
BA
Bretherick AD
CD
Clark DW
SX
Shen X
ET
Esko T
KZ
Kutalik Z
WJ
Wilson JF
JP
Joshi PK
Chapter II

Abstract

Summary of the research findings

We use a genome-wide association of 1 million parental lifespans of genotyped subjects and data on mortality risk factors to validate previously unreplicated findings near CDKN2B-AS1, ATXN2/BRAP, FURIN/FES, ZW10, PSORS1C3, and 13q21.31, and identify and replicate novel findings near ABO, ZC3HC1, and IGF2R. We also validate previous findings near 5q33.3/EBF1 and FOXO3, whilst finding contradictory evidence at other loci. Gene set and cell-specific analyses show that expression in foetal brain cells and adult dorsolateral prefrontal cortex is enriched for lifespan variation, as are gene pathways involving lipid proteins and homeostasis, vesicle-mediated transport, and synaptic function. Individual genetic variants that increase dementia, cardiovascular disease, and lung cancer - but not other cancers - explain the most variance. Resulting polygenic scores show a mean lifespan difference of around five years of life across the deciles.

at least 500,193 European ancestry offspring

Chapter III

Study Statistics

Key metrics and study information

500193
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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