No association of complexin1 and complexin2 genes with schizophrenia in a Japanese population

被引:9
|
作者
Kishi, T
Ikeda, M
Suzuki, T
Kitajima, T
Yamanouchi, Y
Kinoshita, Y
Ozaki, N
Iwata, N [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Psychiat, Toyoake, Aichi 4701192, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Psychiat, Nagoya, Aichi 4668850, Japan
关键词
schizophrenia; complexin; linkage disequilibrium; haplotype-tagging SNP;
D O I
10.1016/j.schres.2005.12.842
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Several investigations suggest that complexin may be a schizophrenia-SUsceptibility factor. We conducted a genetic association analysis between complexin genes (CPLX1 and CPLX2) and schizophrenia in Japanese patients (377 cases and 341 controls). Tell and eleven haplotype-tagging (ht)SNPs in CPLX1 and CPLX2, respectively, were selected. Only one htSNP (rs930047 in CPLX2) in allele-wise analysis showed significance, and even this disappeared with an increased sample size (563 cases and 519 controls: P=.757). Haplotype-wise analysis showed a weak association with a combination of htSNPs in CPLX2 (P=.0424), but this may be a result of type I error due to multiple testing. Our results suggest that complexin genes do not play a major role in sell izophrenia in Japanese patients. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 189
页数:5
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