The −1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD
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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In humans, lower activity of dopamine β-hydroxylase is associated with poor sustained attention, poor executive function, and impulsiveness.
“In humans, lower activity of dopamine β-hydroxylase, the enzyme that synthesizes NE, is associated with poor sustained attention (Greene et al., 2009), poor executive function (Kieling et al., 2008), and impulsiveness (Hess et al., 2009)”
From Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders (2011) · cites this paper as Kieling et al., 2008
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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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