Cited by 65Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on BehaviorSchizophrenia research and treatment

The −1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD

Kieling, Christian, Genro, Júlia P., Hutz, Mara H., Rohde, Luis Augusto·2008·American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Abstract

Catecholaminergic imbalance has increasingly been implicated in the pathophysiology of attention‐deficit/hyperactivity disorder (ADHD). The enzyme dopamine‐β‐hydroxylase (DβH)—critical to catecholaminergic regulation—is under strong genetic control, with the −1021 C/T polymorphism accounting for up to 50% of the enzymatic activity. This work aimed to investigate association between this functional polymorphism and the performance of children and adolescents with ADHD in neuropsychological measures of executive function (EF). Sixty‐four drug‐naïve patients with ADHD undertook a Continuous Performance Test and the Wisconsin Card Sorting Test. By means of a factorial analysis, a composite measure of EF was extracted. Performance according to genotypic group was analyzed, including age as a confounder. In addition, a family‐based association test was conducted as a confirmatory analysis. Principal components analysis of neuropsychological measures loaded two factors that explained 83.8% of total variance. Cognitive performance, as measured by the composite score, showed significant difference between genotypic groups after adjustment for age (P = 0.002). The CC homozygosity was associated with a diminished global EF performance, a result that was corroborated by the intra‐familial analysis. The present study demonstrated an association between the neuropsychological performance of children with ADHD and a functional polymorphism in the promoter region of the DBH gene. The refinement of the ADHD phenotype by means of composite measures of EF can contribute to uncover the molecular underpinnings of ADHD. © 2007 Wiley‐Liss, Inc.

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Crossref · 10.1002/ajmg.b.30636

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References 60 · Cited by 65

Authors
Kieling, C., Genro, J. P., Hutz, M. H., & Rohde, L. A.
Affiliations
Universidade Federal do Rio Grande do Sul (BR)
Venue
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Publisher
Wiley
Published
2008-05-20
Volume
147B
Issue
4
Pages
485-490
ISSN
  • 1552-4841 (ISSN-L)
  • 1552-485X
OpenAlex
W2144432427
Cited by
65
References
60
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 3 · 2021: 3 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 3 · 2015: 2 · 2014: 2 · 2013: 3 · 2012: 10
FWCI
3.03
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Medical Genetics Part B Neuropsychiatric Genetics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico
  • Hospital de Clínicas de Porto Alegre
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Keywords
attention deficit hyperactivity disorder, dopamine beta-hydroxylase, promoter, executive function, neuropsychological performance, children and adolescents, family-based association, continuous performance test, Wisconsin Card Sorting Test, genetic association
MeSH terms
Adolescent, Attention Deficit Disorder with Hyperactivity, Child, Cognition, Dopamine beta-Hydroxylase, Genotype, Humans, Neuropsychological Tests, Nuclear Family, Promoter Regions, Genetic, Polymorphism, Single Nucleotide

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