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PMID: 18553640 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD.

Zhou K, Chen W, Buitelaar J, Banaschewski T, Oades RD, Franke B, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Lasky-Su J, Taylor E, Brookes KJ, Xu X, Neale BM, Rijsdijk F, Thompson M, Asherson P, Faraone SV

Abstract

Previous studies have found heterogeneous association between DAT1-3'-UTR-VNTR and attention deficit hyperactivity disorder (ADHD). Various proportions of conduct disorder (CD) comorbidity in their ADHD samples may partially explain the observational discrepancies. Evidence for this comes from family and twin studies which found ADHD probands with CD (ADHD + CD) are genetically different from those without CD (ADHD - CD). Genotypes of 20 DAT1 markers were analyzed in 576 trios, consisting of 141 ADHD + CD and 435 ADHD - CD. In addition to the classical TDT test, a specific genetic heterogeneity test was performed to identify variants that have different transmission patterns in the two phenotypic subgroups. After multiple-test correction, rs40184 and rs2652511 were significant in TDT tests. Further heterogeneity test found the two SNPs had a significant transmission pattern difference between ADHD + CD and ADHD - CD children, indicating that DAT1 has a significantly greater genetic influence on ADHD without CD. Although the result needs further replications, it does highlight the importance of selecting genetically homogeneous samples for molecular genetic analyses of ADHD.

MeSH Terms
Alleles Attention Deficit Disorder with Hyperactivity/diagnosis,genetics Chi-Square Distribution Child Comorbidity Conduct Disorder/epidemiology,genetics Dopamine Plasma Membrane Transport Proteins/genetics Europe/epidemiology Female Gene Frequency Genetic Heterogeneity Genetic Markers Genotype Haplotypes Humans Incidence Linkage Disequilibrium Male Polymorphism, Single Nucleotide
Chemicals
Dopamine Plasma Membrane Transport Proteins Genetic Markers SLC6A3 protein, human
Authors & Affiliations
26 authors, click to expand affiliations / ORCID
Zhou Kaixin
MRC Social Genetic Developmental and Psychiatry Centre, Institute of Psychiatry, London, United Kingdom.
Chen Wai
Buitelaar Jan
Banaschewski Tobias
Oades Robert D
Franke Barbara
Sonuga-Barke Edmund
Ebstein Richard
Eisenberg Jacques
Gill Michael
Manor Iris
Miranda Ana
Mulas Fernando
Roeyers Herbert
Rothenberger Aribert
Sergeant Joseph
Steinhausen Hans-Christoph
Lasky-Su Jessica
Taylor Eric
Brookes Keeley J
Xu Xiaohui
Neale Benjamin M
Rijsdijk Fruhling
Thompson Margaret
Asherson Philip
Faraone Stephen V
Article Info
Journal
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Abbr.
Am J Med Genet B Neuropsychiatr Genet
ISSN
1552-485X
Published
2008-12-05
Pages
1481-7
Language
English
Region
United States
NLM ID
101235742
Subset
IM
Grants
NIMH NIH HHS · R01 MH062873 · United States
NIMH NIH HHS · R01 MH081803 · United States
NIMH NIH HHS · R01MH62873 · United States
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