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Selective role for the COMT polymorphism in a trans-diagnostic compulsivity phenotype.

Accepted version
Peer-reviewed

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Type

Article

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Authors

Chamberlain, Samuel R 
Grant, Jon E 

Abstract

BACKGROUND: Impulsivity and compulsivity are central to understanding a range of psychiatric disorders but also to understanding the spectrum of normative human behavior. It was recently shown that separable latent phenotypes of impulsivity and compulsivity could be fractionated. The possible genetic contributions to these latent phenotypes have yet to be elicited. The catechol-o-methyl transferase (COMT) Val158Met polymorphism (rs4680) regulates cortical dopamine degradation and is a key area of interest in this context. METHODS: COMT Val158Met polymorphism status was obtained from a random subset (n = 258) of young adults from an established cohort, for whom latent phenotype scores were previously reported. Differences in latent phenotype scores were explored between COMT groups using analysis of variance (ANOVA) and post-hoc t tests. RESULTS: The Val-Val subgroup exhibited significantly elevated compulsivity scores compared to both other groups. Impulsivity scores did not differ significantly as a function of COMT Val158Met polymorphism status. CONCLUSIONS: These results suggest that the COMT polymorphism, and by implication cortical dopamine degradation, influences the expression of a trans-diagnostic compulsivity phenotype, even accounting for possible confounding effects of impulsivity.

Description

Keywords

Adult, Catechol O-Methyltransferase, Cohort Studies, Compulsive Behavior, Humans, Impulsive Behavior, Young Adult

Journal Title

Psychol Med

Conference Name

Journal ISSN

0033-2917
1469-8978

Volume Title

48

Publisher

Cambridge University Press (CUP)
Sponsorship
Wellcome Trust (110049/Z/15/Z)
Wellcome Trust