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

Transl Psychiatry. 2018 Sep 4;8(1):178. doi: 10.1038/s41398-018-0236-1.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Attention Deficit Disorder with Hyperactivity / epidemiology
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Biological Specimen Banks
  • Bipolar Disorder / epidemiology
  • Bipolar Disorder / genetics*
  • Calcium-Binding Proteins / genetics
  • Female
  • Gene Expression
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study*
  • Humans
  • Hydrolases
  • Magnetic Resonance Imaging
  • Male
  • Microtubule-Associated Proteins
  • Middle Aged
  • Multifactorial Inheritance
  • Nerve Tissue Proteins / genetics
  • Polymorphism, Single Nucleotide
  • Risk-Taking*
  • Schizophrenia / epidemiology
  • Schizophrenia / genetics*
  • Self Report
  • United Kingdom / epidemiology
  • White Matter / diagnostic imaging

Substances

  • CGREF1 protein, human
  • Calcium-Binding Proteins
  • Microtubule-Associated Proteins
  • Nerve Tissue Proteins
  • DPYSL5 protein, human
  • Hydrolases