Association of a 5-HT1Dβ Receptor Gene Polymorphism with Obsessive-Compulsive Disorder in Korean Male Subjects

被引:10
|
作者
Kim, Se Joo [1 ,2 ]
Namkoong, Kee [1 ,2 ]
Kang, Jee In [1 ,2 ,3 ]
Kim, Chan-Hyung [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Psychiat, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Inst Behav Sci Med, Seoul, South Korea
[3] Ilsan Hosp, Natl Hlth Insurance Corp, Dept Psychiat, Gyeonggi Do, South Korea
关键词
5-HT1D beta receptor gene; Obsessive-compulsive disorder; Single nucleotide polymorphism; FAMILY-BASED ASSOCIATION; SYMPTOM DIMENSIONS; ALCOHOL DEPENDENCE; CANDIDATE GENES; NO ASSOCIATION; SEROTONIN; GENDER; PATHOGENESIS; SUMATRIPTAN; DEPRESSION;
D O I
10.1159/000209861
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 5-HT1D beta receptor gene appears to be particularly interesting in the pathophysiology of obsessive-compulsive disorder (OCD). The 5-HT1D beta receptor is a terminal autoreceptor involved in the regulation of serotonin synthesis and release. We performed an association study of the G861C single nucleotide polymorphism (SNP) of the 5-HT1D beta receptor in 167 male Korean OCD subjects and in 107 controls. Individuals with the G allele had an increased chance of having OCD (OR 1.49, 95% CI 1.05-2.10). Our findings suggest an association between the G861C SNP of the 5-HT1D beta receptor and males with OCD. In the future, other tag SNPs that cover the entire 5-HT1D beta gene region as well as additional SNPs that are supposed to have meaningful functions should be investigated in both male and female OCD subjects. Copyright (C) 2009 S. Karger AG, Basel
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页码:96 / 99
页数:4
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