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GWAS Study

Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression.

Strawbridge RJ, Ward J, Lyall LM et al.

30181555 PubMed ID
GWAS Study Type
400687 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SR
Strawbridge RJ
WJ
Ward J
LL
Lyall LM
TE
Tunbridge EM
CB
Cullen B
GN
Graham N
FA
Ferguson A
JK
Johnston KJA
LD
Lyall DM
MD
Mackay D
CJ
Cavanagh J
HD
Howard DM
AM
Adams MJ
DI
Deary I
EV
Escott-Price V
OM
O'Donovan M
MA
McIntosh AM
BM
Bailey MES
PJ
Pell JP
HP
Harrison PJ
SD
Smith DJ
Chapter II

Abstract

Summary of the research findings

Risk-taking behaviour is an important component of several psychiatric disorders, including attention-deficit hyperactivity disorder, schizophrenia and bipolar disorder. Previously, two genetic loci have been associated with self-reported risk taking and significant genetic overlap with psychiatric disorders was identified within a subsample of UK Biobank. Using the white British participants of the full UK Biobank cohort (n = 83,677 risk takers versus 244,662 controls) for our primary analysis, we conducted a genome-wide association study of self-reported risk-taking behaviour. In secondary analyses, we assessed sex-specific effects, trans-ethnic heterogeneity and genetic overlap with psychiatric traits. We also investigated the impact of risk-taking-associated SNPs on both gene expression and structural brain imaging. We identified 10 independent loci for risk-taking behaviour, of which eight were novel and two replicated previous findings. In addition, we found two further sex-specific risk-taking loci. There were strong positive genetic correlations between risk-taking and attention-deficit hyperactivity disorder, bipolar disorder and schizophrenia. Index genetic variants demonstrated effects generally consistent with the discovery analysis in individuals of non-British White, South Asian, African-Caribbean or mixed ethnicity. Polygenic risk scores comprising alleles associated with increased risk taking were associated with lower white matter integrity. Genotype-specific expression pattern analyses highlighted DPYSL5, CGREF1 and C15orf59 as plausible candidate genes. Overall, our findings substantially advance our understanding of the biology of risk-taking behaviour, including the possibility of sex-specific contributions, and reveal consistency across ethnicities. We further highlight several putative novel candidate genes, which may mediate these genetic effects.

83,677 British ancestry cases, 244,662 British ancestry controls

Chapter III

Study Statistics

Key metrics and study information

400687
Total Participants
GWAS
Study Type
Yes
Replicated
2,764 South Asian ancestry cases, 3,139 African Caribbean ancestry cases, 16,169 European ancestry cases, 3,866 mixed ancestry cases, 4,267 South Asian ancestry controls, 4,341 African Caribbean ancestry controls, 31,814 European ancestry controls, 5,988 mixed ancestry controls
Replication Participants
African American or Afro-Caribbean, European, South Asian
Ancestry
Chapter IV

AI-Generated Summary

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