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突触结合蛋白III基因多态性与精神分裂症

Synapsin III gene polymorphisms and schizophrenia.

作者信息

Ohmori O, Shinkai T, Hori H, Kojima H, Nakamura J

机构信息

Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Neurosci Lett. 2000 Jan 28;279(2):125-7. doi: 10.1016/s0304-3940(99)00970-2.

Abstract

Synapsins are synaptic vesicle-associated phosphoproteins and are thought to play crucial roles in synaptogenesis and neurotransmitter release. Synaptic abnormalities have been reported in the pathophysiology of schizophrenia. In addition, the synapsin III gene, a member of the synapsin gene family, has been located at 22q12-13, which has been suggested as a potential susceptibility locus for schizophrenia. We investigated a genetic association between schizophrenia and the synapsin III gene polymorphisms (-631C/G and -196G/A) in 160 schizophrenic patients and 153 controls. No significant positive association between either polymorphism and schizophrenia was observed. Furthermore, no significant association was observed between either polymorphism and the diagnostic subtypes. Our results suggested that the synapsin III gene polymorphisms do not confer increased susceptibility to schizophrenia.

摘要

突触结合蛋白是与突触小泡相关的磷蛋白,被认为在突触形成和神经递质释放中起关键作用。在精神分裂症的病理生理学中已报道存在突触异常。此外,突触结合蛋白III基因是突触结合蛋白基因家族的成员,定位于22q12 - 13,这一区域被认为是精神分裂症的一个潜在易感位点。我们在160例精神分裂症患者和153例对照中研究了精神分裂症与突触结合蛋白III基因多态性(-631C/G和-196G/A)之间的遗传关联。未观察到任何一种多态性与精神分裂症之间存在显著的正相关。此外,也未观察到任何一种多态性与诊断亚型之间存在显著关联。我们的结果表明,突触结合蛋白III基因多态性不会增加患精神分裂症的易感性。

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