3.8 Article

GABA-A receptor β3 and α5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder:: A genetic association study

期刊

AMERICAN JOURNAL OF MEDICAL GENETICS
卷 105, 期 4, 页码 317-320

出版社

WILEY-LISS
DOI: 10.1002/ajmg.1354

关键词

association study; gamma-aminobutyric acid (GABA); GABA-A receptor beta 3 subunit gene (GABRB3); chromosome 15; bipolar affective disorder

向作者/读者索取更多资源

There is accumulated evidence that the genes coding for the receptor of gamma aminobutyric acid (GABA), the most important inhibitory neurotransmitter in the CNS, may be involved in the pathogenesis of affective disorders. In a previous study, we have found a genetic association between the GABA-A receptor alpha5 subunit gene locus (GABRA5) on chromosome 15q11-q13 and bipolar affective disorder, The aim of the present study was to examine the same subjects to see if there exists a genetic association between bipolar affective disorder and the GABA receptor beta3 subunit gene (GABRB3), which is located within 100 kb from GABRA5, The sample consisted of 48 bipolar patients compared to 44 controls (blood donors), All subjects were Greek, unrelated, and personally interviewed, Diagnosis was based on DSM-IV and ICD-IO criteria, The marker used was a dinucleotide (CA) repeat polymorphism with 12 alleles 179 to 201 bp long; genotyping was successful in all patients and 43 controls. The distribution of GABRB3 genotypes among the controls did not deviate significantly from the Hardy-Weinberg equilibrium, No differences in allelic frequencies between bipolar patients and controls were found for GABRB3, while this locus and GABRA5 did not seem to be in significant linkage disequilibrium, In conclusion, the GABRB3 CA-repeat polymorphism we investigated does not present the observed association between bipolar affective illness and GABRA5. This could be due to higher mutation rate in the GABRB3 CA-repeat polymorphism, but it might also signify that GABRA5 is the gene actually associated with the disease. (C) 2001 Wiley-Liss, Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据