Sex Differences in COMT Polymorphism Effects on Prefrontal Inhibitory Control in Adolescence

  • Thomas P White
  • Eva Loth
  • Lydia Krabbendam
  • Katya Rubia
  • Robert Whelan
  • Tobias Banaschewski
  • Gareth J Barker
  • Arun Lw Bokde
  • Christian Büchel
  • Patricia Conrod
  • Herta Flor
  • Vincent Frouin
  • Andreas Heinz
  • Hugh Garavan
  • Penny Gowland
  • Bernd Ittermann
  • Claire Lawrence
  • Karl Mann
  • Marie-Laure Paillère
  • Frauke Nees
  • Tomas Paus
  • Zdenka Pausova
  • Marcella Rietschel
  • Trevor Robbins
  • Mira Fauth-Bühler
  • Michael N Smolka
  • Jürgen Gallinat
  • Sukhwinder S Shergill
  • Gunter Schumann

Related Research units

Abstract

Catecholamine-0-methyl-transferase (COMT) gene variation effects on prefrontal blood oxygenation-level dependent (BOLD) activation are robust; however, despite observations that COMT is oestrogenically catabolised, sex differences in its prefrontal repercussions remain unclear. Here, in a large sample of healthy adolescents stratified by sex and Val(158)Met genotype (n=1133) we examine BOLD responses during performance of the stop-signal task in right-hemispheric prefrontal regions fundamental to inhibitory control. A significant sex-by-genotype interaction was observed in pre-SMA during successful-inhibition trials and in both pre-SMA and inferior frontal cortex during failed-inhibition trials with Val-homozygotes displaying elevated activation compared to other genotypes in males but not in females. BOLD activation in the same regions significantly mediated the relationship between COMT genotype and inhibitory proficiency as indexed by stop-signal reaction time in males alone. These sexually-dimorphic effects of COMT on inhibitory brain activation have important implications for our understanding of the contrasting patterns of prefrontally-governed psychopathology observed in males and females.Neuropsychopharmacology accepted article preview online, 13 May 2014; doi:10.1038/npp.2014.107.

Bibliographical data

Original languageEnglish
ISSN0893-133X
DOIs
Publication statusPublished - 2014
PubMed 24820538