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PMID: 16941663 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects.

Li J, Wang Y, Zhou R, Zhang H, Yang L, Wang B, Faraone SV

Abstract

Prior work has shown reduced serotonin transmission to be associated with impulsivity and behavioral problems. The current study assessed the association between ADHD and two variants of the serotonin transporter gene: the 44-bp deletion/insertion polymorphism (5-HTTLPR) and the 17 bp-repeat polymorphism in intron 2 (STin2.VNTR). We hypothesized that ADHD phenotypes associated with impulsivity would show an association with these variants. Two-hundred and ninety-three ADHD trios were genotyped and analyzed using transmission disequilibrium test (TDT) analysis and haplotype analysis. We found no association between the STin2.VNTR and ADHD, but did find preferential transmission of the S allele of the 5-HTTLPR polymorphism (chi(2) = 5.751, P = 0.016) to probands with ADHD. Haplotype analysis found the L/10 haplotype was over-transmitted (chi(2) = 6.172, P = 0.013), while L/12 was under-transmitted to probands with ADHD (chi(2) = 4.866, P = 0.027).

MeSH Terms
Alleles Asians/genetics Attention Deficit Disorder with Hyperactivity/classification,genetics,metabolism Base Sequence Child China DNA/genetics Female Gene Frequency Genotype Haplotypes Humans Introns Male Minisatellite Repeats Phenotype Polymorphism, Genetic Receptors, Serotonin/genetics
Chemicals
Receptors, Serotonin DNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Li Jun
Institute of Mental Health, Peking University, Peking University Sixth Hospital, Beijing, PR China.
Wang Yufeng
Zhou Rulun
Zhang Haobo
Yang Li
Wang Bing
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
1552-4841
Published
2007-01-05
Pages
14-9
Language
English
Region
United States
NLM ID
101235742
Subset
IM
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