Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults

Author:

Deng Wei Q.12ORCID,Belisario Kyla12,Gray Joshua C.3,Levitt Emily E.12,Mohammadi‐Shemirani Pedrum4,Singh Desmond15,Pare Guillaume46ORCID,MacKillop James12ORCID

Affiliation:

1. Peter Boris Centre for Addictions Research St. Joseph's Healthcare Hamilton Hamilton Ontario Canada

2. Department of Psychiatry and Behavioural Neurosciences McMaster University Hamilton Canada

3. Department of Medical and Clinical Psychology Uniformed Services University Bethesda Maryland USA

4. Department of Pathology and Molecular Medicine McMaster University Hamilton Canada

5. Department of Biology University of Waterloo Wterloo Canada

6. Department of Health Research Methods, Evidence, and Impact McMaster University Hamilton Canada

Abstract

AbstractImpulsivity refers to a number of conceptually related phenotypes reflecting self‐regulatory capacity that are considered promising endophenotypes for mental and physical health. Measures of impulsivity can be broadly grouped into three domains, namely, impulsive choice, impulsive action, and impulsive personality traits. In a community‐based sample of ancestral Europeans (n = 1534), we conducted genome‐wide association studies (GWASs) of impulsive choice (delay discounting), impulsive action (behavioral inhibition), and impulsive personality traits (UPPS‐P), and evaluated 11 polygenic risk scores (PRSs) of phenotypes previously linked to self‐regulation. Although there were no individual genome‐wide significant hits, the neuroticism PRS was positively associated with negative urgency (adjusted R2 = 1.61%, p = 3.6 × 10−7) and the educational attainment PRS was inversely associated with delay discounting (adjusted R2 = 1.68%, p = 2.2 × 10−7). There was also evidence implicating PRSs of attention‐deficit/hyperactivity disorder, externalizing, risk‐taking, smoking cessation, smoking initiation, and body mass index with one or more impulsivity phenotypes (adjusted R2s: 0.35%–1.07%; FDR adjusted ps = 0.05–0.0006). These significant associations between PRSs and impulsivity phenotypes are consistent with established genetic correlations. The combined PRS explained 0.91%–2.46% of the phenotypic variance for individual impulsivity measures, corresponding to 8.7%–32.5% of their reported single‐nucleotide polymorphism (SNP)‐based heritability, suggesting a non‐negligible portion of the SNP‐based heritability can be recovered by PRSs. These results support the predictive validity and utility of PRSs, even derived from related phenotypes, to inform the genetics of impulsivity phenotypes.

Publisher

Wiley

Subject

Behavioral Neuroscience,Neurology,Genetics

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