Association between a novel polymorphism in the promoter region of the neuropeptide Y gene and schizophrenia in humans

被引:67
作者
Itokawa, M
Arai, M
Kato, S
Ogata, Y
Furukawa, A
Haga, S
Ujike, H
Sora, I
Ikeda, K
Yoshikawa, T
机构
[1] Tokyo Inst Psychiat, Dept Schizophrenia Res, Tokyo 1568585, Japan
[2] Tokyo Metropolitan Matsuzawa Hosp, Dept Psychiat, Tokyo 1560057, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept NeuroPsycho Dynam, Okayama 7008530, Japan
[4] Tohoku Univ, Grad Sch Med, Div Psychobiol, Dept Neurosci, Sendai, Miyagi 9808574, Japan
基金
日本学术振兴会;
关键词
case-control study; -485C > T polymorphism; luciferase activity; IMR-32; cell; 1128T > C (Leu7Pro) polymorphism; Japanese;
D O I
10.1016/S0304-3940(03)00718-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hypoactivity of neuropeptide Y (NPY) is thought to be involved in the pathophysiology of schizophrenia, because post-mortem brain studies revealed a decrease of the NPY in schizophrenia, and antipsychotic treatments increase the NPY in animal brains and in cerebrospinal fluid of patients. We performed genetic analysis of the NPY gene in schizophrenia. Mutation screening of the gene detected nine single nucleotide polymorphisms, of which we typed a -485C > T variation from potential functional relevance. The -485T allele was overly represented in the disease group (P = 0.0043). An in vitro promoter assay revealed that a C to T change at nt -485 significantly reduced transcriptional activity. These results suggest that the -485T allele in NPY may confer susceptibility to schizophrenia by decreasing the neuropeptide in brains. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:202 / 204
页数:3
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