Effect of dopamine transporter genotype on caudate volume in childhood ADHD and controls
Open accessAbstract
Polymorphism of the dopamine transporter genotype (DAT1) confers a small but significant susceptibility to attention deficit hyperactivity disorder (ADHD). We examined whether the volume of the head of caudate, a striatal structure with high DAT expression that is important for inhibitory function, differs by DAT1 in children diagnosed with the disorder relative to age and IQ matched controls. Volume of the head of caudate was delineated in the right and left hemisphere and compared between 7‐ and 13‐year‐old children with and without ADHD (combined type) who were carriers of two (10/10) or one (9/10) copy of the 10‐repeat DAT1 allele. Caudate volumes were overall smaller in 10/10 than 9/10 children, particularly in the left than right hemisphere. While DAT1 effects did not vary by ADHD diagnosis, overall caudate volumes were smaller in ADHD relative to control children. Altered caudate development associated with 10‐repeat homozygosity of DAT1 may contribute susceptibility to ADHD. © 2010 Wiley‐Liss, Inc.
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The caudate nucleus is a core region of the dopamine reward-circuit, implicated in ADHD-control differences, and genetic variation in DAT1 is reported to affect its function and structure.
“The caudate nucleus is a core region of the dopamine reward-circuit,42 implicated in ADHD-control differences,4 and genetic variation in DAT1 is reported to affect its function and structure 26,43”
From Striatal sensitivity during reward processing in attention-deficit/hyperactivity disorder (2012) · cites this paper as [43]
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Changes in the Development of Striatum Are Involved in Repetitive Behavior in Autism
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- Authors
- Shook, D., Brady, C., Lee, P. S., Kenealy, L., Murphy, E. R., Gaillard, W. D., VanMeter, J. W., Cook, E. H., Stein, M., & Vaidya, C. J.
- Affiliations
- Georgetown University (US)
- Children's National (US)
- Georgetown University Medical Center (US)
- University of Illinois Chicago (US)
- Corresponding author
- Vaidya, Chandan J.
- ORCID
- Venue
- American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Publisher
- Wiley
- Published
- 2010-10-18
- Volume
- 156
- Issue
- 1
- Pages
- 28-35
- ISSN
- 1552-4841 (ISSN-L)
- 1552-485X
- PMC
- PMC3010298
- OpenAlex
- W2111341053
- Cited by
- 31
- References
- 53
- Citations by year
- 2023: 1 · 2022: 3 · 2021: 2 · 2018: 1 · 2017: 3 · 2016: 7 · 2015: 2 · 2014: 2 · 2013: 4 · 2012: 4
- FWCI
- 2.40
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Georgetown University
- National Institute of Mental Health (MH 065395, MH70564, R01MH065395, R01MH070564)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- attention deficit hyperactivity disorder, dopamine transporter, DAT1 polymorphism, caudate volume, striatum, brain structure, genetic susceptibility, combined type ADHD, children, hemispheric lateralization, inhibitory function
- MeSH terms
- Adolescent, Attention Deficit Disorder with Hyperactivity, Brain Mapping, Caudate Nucleus, Child, Demography, Female, Genotype, Humans, Male, Organ Size, Case-Control Studies, Dopamine Plasma Membrane Transport Proteins
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