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精神分裂症与睫状神经营养因子基因缺失突变

Schizophrenic psychoses and the CNTF null mutation.

作者信息

Tanaka Y, Ujike H, Fujiwara Y, Takeda T, Takehisa Y, Kodama M, Otsuki S, Kuroda S

机构信息

Department of Neuropsychiatry, Okayama University Medical School, Japan.

出版信息

Neuroreport. 1998 Apr 20;9(6):981-3. doi: 10.1097/00001756-199804200-00005.

Abstract

Genetic susceptibility plays an important role in the development of schizophrenic psychoses, and the neural maldevelopment hypothesis is suggested by neuropathological and neuroimaging findings. We investigated the association between a null mutation in the ciliary neurotrophic factor (CNTF) gene and functional psychoses including schizophrenia and schizoaffective disorder. The frequency of mutant allele was significantly increased in patients with schizoaffective disorder, but not in those with schizophrenia in comparison with controls. The CNTF null mutation resulting in CNTF deficiency may confer potential susceptibility to schizoaffective disorder.

摘要

遗传易感性在精神分裂症性精神病的发生发展中起重要作用,神经病理学和神经影像学研究结果提示了神经发育异常假说。我们研究了睫状神经营养因子(CNTF)基因的无效突变与包括精神分裂症和分裂情感性障碍在内的功能性精神病之间的关联。与对照组相比,分裂情感性障碍患者中突变等位基因的频率显著增加,但精神分裂症患者中未增加。导致CNTF缺乏的CNTF无效突变可能使个体对分裂情感性障碍具有潜在易感性。

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