No evidence for an association between variants at the γ-amino-n-butyric acid type A receptor β2 locus and schizophrenia

被引:5
作者
Abou Jamra, Rami
Becker, Tim
Klopp, Norman
Dahdouh, Faten
Schulze, Thomas G.
Gross, Magdalena
Deschner, Monika
Schmael, Christine
Illig, Thomas
Rietschel, Marcella
Propping, Peter
Cichon, Sven
Noethen, Markus M.
Schumacher, Johannes
机构
[1] Univ Bonn, Inst Human Genet, D-53111 Bonn, Germany
[2] Univ Bonn, Inst Med Biometry Informat & Epidemiol, D-53111 Bonn, Germany
[3] Univ Bonn, Dept Psychiat, D-53111 Bonn, Germany
[4] Univ Bonn, Genom Life & Brain Ctr, D-53111 Bonn, Germany
[5] GSF Natl Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
[6] Cent Inst Mental Hlth, Div Genet Epidemiol Psychiat, Mannheim, Germany
关键词
association analysis; gamma-amino-n-loutyric acid type A receptor; schizophrenia;
D O I
10.1097/YPG.0b013e32801118cd
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
The alpha(1)/beta(2)/gamma(2)-containing heteropentamer is the most abundant gamma-amino-n-butyric acid type A receptor subtype in mammalian brains and the corresponding genes, the GABRA1, GABRB2, and GABRG2 genes, are located in chromosomal region 5q34 that several genome wide scans have implicated as a susceptibility region for schizophrenia. Given this positional and functional evidence, Lo et al. (Mol Psychiatry 2004; 9: 603-608) performed systematic linkage disequilibrium mapping of the GABA(A)R gene cluster on 5q34 in 130 schizophrenic patients and 170 controls, all of Chinese Han origin. In the single locus and haplotype analyses, single nucleotide polymorphisms in the GABRB2 gene showed highly significant association. The estimated effect caused by GABRB2 varied between odds ratios of 2.27 and 5.12. In order to re-examine their findings, we analyzed the most significantly associated single nucleotide polymorphism in the GABRB2 gene in a sample of 367 patients with schizophrenia and 360 controls, all of German descent. Our sample had a sufficient power to detect the effects described. Neither single marker nor haplotype analysis revealed a significant association with the disease status. Thus, our results do not support the hypothesis that genetic variation at the GABRB2 locus plays a major role in schizophrenic patients of European descent and that such variation would explain the previously observed linkage findings at this chromosomal region.
引用
收藏
页码:43 / 45
页数:3
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