Source:http://linkedlifedata.com/resource/pubmed/id/21344643
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2011-4-26
|
pubmed:abstractText |
Several studies suggested a genetic component in the etiology of obsessive-compulsive disorder (OCD). COMT involves in the degradation of dopamine and norepinephrin. As another functional SNP locus, COMT -287A/G polymorphism showed an effect on enzyme activity, suggesting that it may influence brain dopamine levels. To identify association of COMT -287A/G polymorphism with susceptibility to OCD in Chinese Han population. We evaluate the genetic contribution of the COMT -287A/G polymorphism in 200 OCD patients and 403 OCD-free control of Chinese Han population by PCR-RFLP. In addition, we investigate whether COMT -287A/G polymorphism is associated with one or more of these symptom dimensions or other characteristics such as sex, age of onset, and tic-relatedness and evaluate the association of the factorial structure of OCD symptoms from the Y-BOCS checklist with the COMT -287A/G polymorphism. A statistical difference was found in the genotypic frequencies of COMT -287A/G between the OCD and control groups (?(2) ?=?13.99, DF?=?2, P?=?0.00091) and in the genotypic frequencies of GG genotype versus AA and AG genotypes of COMT -287 (?(2) ?=?13.49, DF?=?1, P?=?0.00024, OR?=?3.43, 95% CI?=?1.78-6.62). There was a trend for an association in the genotypic distributions of COMT -287A/G polymorphism of males (?(2) ?=?27.81; DF?=?2; P?<?0.001) and females (?(2) ?=?7.31; DF?=?2; P?=?0.026) between the OCD patients and the controls. Using principal component analysis, we derived 5 factors from 12 main contents of OCD symptoms from the Y-BOCS checklist and found no association with COMT -287A/G polymorphism. Our study supports the involvement of the COMT -287A/G polymorphism in the genetic susceptibility to OCD in Chinese Han population.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1552-485X
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Wiley-Liss, Inc.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
156B
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
393-400
|
pubmed:meshHeading |
pubmed-meshheading:21344643-Asian Continental Ancestry Group,
pubmed-meshheading:21344643-Case-Control Studies,
pubmed-meshheading:21344643-Catechol O-Methyltransferase,
pubmed-meshheading:21344643-China,
pubmed-meshheading:21344643-Dopamine,
pubmed-meshheading:21344643-Female,
pubmed-meshheading:21344643-Genetic Predisposition to Disease,
pubmed-meshheading:21344643-Genotype,
pubmed-meshheading:21344643-Humans,
pubmed-meshheading:21344643-Male,
pubmed-meshheading:21344643-Obsessive-Compulsive Disorder,
pubmed-meshheading:21344643-Polymorphism, Single Nucleotide,
pubmed-meshheading:21344643-Principal Component Analysis,
pubmed-meshheading:21344643-Risk Factors,
pubmed-meshheading:21344643-Sex Factors
|
pubmed:year |
2011
|
pubmed:articleTitle |
Association of catechol-O-methyl transferase (COMT) gene -287A/G polymorphism with susceptibility to obsessive-compulsive disorder in Chinese Han population.
|
pubmed:affiliation |
Shandong Provincial Key Laboratory of Metabolic Disease, The Affiliated Hospital of Medical College, Qingdao University, China.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|