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GWAS Study

Rare genetic associations with human lifespan in UK Biobank are enriched for oncogenic genes.

Park J, Peña-Tauber A, Talozzi L et al.

40021682 PubMed ID
GWAS Study Type
393833 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PJ
Park J
PA
Peña-Tauber A
TL
Talozzi L
GM
Greicius MD
LG
Le Guen Y
Chapter II

Abstract

Summary of the research findings

Human lifespan is shaped by genetic and environmental factors. To enable precision health, understanding how genetic variants influence mortality is essential. We conducted a survival analysis in European ancestry participants of the UK Biobank, using age-at-death (N=35,551) and last-known-age (N=358,282). The associations identified were predominantly driven by cancer. We found lifespan-associated loci (APOE, ZSCAN23) for common variants and six genes where burden of loss-of-function variants were linked to reduced lifespan (TET2, ATM, BRCA2, CKMT1B, BRCA1, ASXL1). Additionally, eight genes with pathogenic missense variants were associated with reduced lifespan (DNMT3A, SF3B1, TET2, PTEN, SOX21, TP53, SRSF2, RLIM). Many of these genes are involved in oncogenic pathways and clonal hematopoiesis. Our findings highlight the importance of understanding genetic factors driving the most prevalent causes of mortality at a population level, highlighting the potential of early genetic testing to identify germline and somatic variants increasing one's susceptibility to cancer and/or early death.

393,833 British ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

393833
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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