Association study of the dysbindin (DTNBP1) gene in schizophrenia from the Japanese population

作者：Tochigi Mamoru; Zhang Xuan; Ohashi Jun; Hibino Hiroyuki; Otowa Takeshi; Rogers Mark; Kato Tadafumi; Okazaki Yuji; Kato Nobumasa; Tokunaga Katsushi; Sasaki Tsukasa^*

来源：Neuroscience Research, 2006, 56(2): 154-158.

DOI：10.1016/j.neures.2006.06.009

• dystrobrevin binding protein 1 (DTNBP1)
• schizophrenia
• single nucleotide polymorphism (SNP)
• haplotype
• case-control study
• chromosome 6

Dysbindin (DTNBP1: dystrobrevin binding protein 1), located on 6p22.3, is a candidate susceptibility gene for schizophrenia. Several studies, mostly in Caucasians, have provided evidence for an association between schizophrenia and the gene, although no common polymorphism or haploytpe has been established. In Asian populations, two studies investigated a limited number of single nucleotide polymorphisms (SNPs) of dysbindin and observed support for the association. In the present study, we investigated 12 SNPs of dysbindin, including those examined in previous Asian studies, and the corresponding haplotypes in a Japanese people with schizophrenia. As a result, no significant difference was observed between patients and controls in allelic frequencies or genotypic distributions of the 12 SNPs. Permutation test however showed significant differences in frequencies of the estimated 10-marker haplotypes between patients and controls (global p = 0.006). The present study may provide further support for an association between dysbindin and schizophrenia in Asian populations. The results might be similar to a previous Asian study, but specific haplotypes suggested for the association differed between the studies. Studies with more markers and subjects may be required before firm conclusions can be reached.

• 出版日期2006-10
• 单位吉林大学