Dopamine transporter 3'UTR VNTR genotype is a marker of performance on executive function tasks in children with ADHD
Open Access
- 17 June 2008
- journal article
- research article
- Published by Springer Nature in BMC Psychiatry
- Vol. 8 (1) , 1-9
- https://doi.org/10.1186/1471-244x-8-45
Abstract
Background: Attention-Deficit/Hyperactivity Disorder (ADHD) is a heterogeneous disorder from both clinical and pathogenic viewpoints. Executive function deficits are considered among the most important pathogenic pathways leading to ADHD and may index part of the heterogeneity in this disorder. Methods: To investigate the relationship between the dopamine transporter gene (SLC6A3) 3'-UTR VNTR genotypes and executive function in children with ADHD, 196 children diagnosed with ADHD were sequentially recruited, genotyped, and tested using a battery of three neuropsychological tests aimed at assessing the different aspects of executive functioning. Results: Taking into account a correction for multiple comparisons, the main finding of this study is a significant genotype effect on performances on the Tower of London (F = 6.902, p = 0.009) and on the Wechsler Intelligence Scale for Children, Third Edition (WISC-III) Freedom From Distractibility Index (F = 7.125, p = 0.008), as well as strong trends on Self Ordered Pointing Task error scores (F = 4,996 p = 0.026) and WISC-III Digit Span performance (F = 6.28, p = 0.023). Children with the 9/10 genotype exhibited, on average, a poorer performance on all four measures compared to children with the 10/10 genotype. No effect of genotype on Wisconsin Card Sorting Test measures of performance was detected. Conclusion: Results are compatible with the view that SLC6A3 genotype may modulate components of executive function performance in children with ADHD.Keywords
This publication has 52 references indexed in Scilit:
- The reliability and validity of the self-ordered pointing taskArchives of Clinical Neuropsychology, 2007
- An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to adulthoodAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2006
- Additive Effects of Genetic Variation in Dopamine Regulating Genes on Working Memory Cortical Activity in Human BrainJournal of Neuroscience, 2006
- Striatal dopamine transporter density in drug naive patients with attention-deficit/hyperactivity disorderNuclear Medicine Communications, 2006
- Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sampleMolecular Psychiatry, 2005
- Executive dysfunction in Parkinson's disease is associated with altered pallidal–frontal processingNeuroImage, 2005
- Differential effects of DRD4 and DAT1 genotype on fronto-striatal gray matter volumes in a sample of subjects with attention deficit hyperactivity disorder, their unaffected siblings, and controlsMolecular Psychiatry, 2005
- Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samplesMolecular Psychiatry, 2001
- Perceived Family Functioning, Marital Status, and Depression in Parents of Boys with Attention Deficit DisorderJournal of Learning Disabilities, 1989
- Deficits on subject-ordered tasks after frontal- and temporal-lobe lesions in manNeuropsychologia, 1982