Abstract

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.

Highlights

  • Introduction The Research DomainCriteria approach proposes studying traits existing in the general population to better understand psychopathology

  • For single nucleotide polymorphism (SNP) showing significant eQTLs in the Lieber Institute for Brain Development (LIBD) dataset, we looked for replication in the CommonMind Consortium (CMC) dorsolateral prefrontal cortex (DLPFC) RNA-Seq data (n = 547)[27], using the LIBD eQTL

  • Examining the biology of risk-taking behaviour has the potential to improve our understanding of the pathophysiology of psychiatric disorders such as attention-deficit hyperactivity disorder (ADHD), SCZ and bipolar disorder (BD), as well as problem behaviours such as drug and alcohol misuse

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Summary

Introduction

Criteria approach proposes studying traits existing in the general population (rather than categorical diagnoses) to better understand psychopathology. One such trait is risk-taking behaviour, a key component of psychiatric disorders such as attention-. Risk taking is observed in schizophrenia (SCZ), cognitive difficulties[4,5] may confound this relationship. Problem behaviours such as smoking and drug and alcohol misuse[6,7] frequently co-occur with psychiatric disorders and might be considered a consequence of risk-taking behaviour. It is likely that genetic predisposition to risk-taking behaviour impacts on brain structure and function

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