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Irish Child Health Database - Peer Reviewed Papers

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  • The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD

    Published in:

    Exp Brain Res, Vol: 163, Page: 352-60

    Publication Date:

    June 2005

    Aims & Objectives:

    The aim of this study was to examine the association of methionine allele of the COMT polymorphism which impairs prefrontal cognition in children and adolescents with attention-deficit hyperactivity disorder

    Abstract:

    ADHD is a highly heritable psychiatric disorder of childhood. A functional polymorphism (Val158Met) of the catechol-O-methyltransferase (COMT) gene has attracted interest as a candidate gene for ADHD. The high-activity valine variant of this polymorphism degrades prefrontal dopamine three to four times more quickly than the low-activity methionine variant and could therefore contribute to the proposed hypodopaminergic state in ADHD. Here we tested for association of this polymorphism with ADHD and examined its influence on prefrontal cognition in ADHD. We have previously reported no association of the Val158Met COMT gene polymorphism in 94 Irish ADHD families (Hawi et al. (2000) Am J Med Genet 96:282-284). Here we re-examined this finding with an extended sample of 179 ADHD cases using a family control design. We also examined the performance of children and adolescents with ADHD (n = 61) on a standardised test of sustained attention. Analysis confirmed the absence of an association between the Val158Met COMT gene polymorphism and the clinical phenotype of ADHD. COMT genotype, however, affected prefrontal cognition in ADHD: ADHD children who were homozygous for the valine variant had significantly better sustained attention than those ADHD children possessing at least one copy of the methionine variant. Children possessing the methionine variant performed significantly below age-related norms on tests of sustained attention. Contrary to expectations, the methionine variant of the Val158Met COMT gene polymorphism impaired prefrontally-mediated cognition in ADHD. This effect may be understood by positing a hyper-functioning of prefrontal dopaminergic systems. Against this background, the slower clearance of dopamine associated with the methionine variant of the COMT gene polymorphism may be disadvantageous to cognition in ADHD.

    Authors:

    M. A. Bellgrove; K. Domschke; Z. Hawi; A. Kirley; C. Mullins; I. H. Robertson; M. Gill

    Study Type:

    Study Papers » Case Study » Descriptive Studies - Without a comparision

    Categories:

    attention-deficit hyperactivity disorder

    International Classification:

    Mental and behavioural disorders - Behavioural and emotional disorders with onset usually occurring in childhood and adolescence - attention-deficit hyperactivity disorder

    Keywords:


    Geography:

    Republic of Ireland (Nationwide)