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III 型代谢型谷氨酸受体基因 GRM4 和 GRM7 多态性与精神分裂症的关联研究。

Association study of polymorphisms in the group III metabotropic glutamate receptor genes, GRM4 and GRM7, with schizophrenia.

作者信息

Shibata Hiroki, Tani Ayako, Chikuhara Tomoyuki, Kikuta Rumiko, Sakai Mayumi, Ninomiya Hideaki, Tashiro Nobutada, Iwata Nakao, Ozaki Norio, Fukumaki Yasuyuki

机构信息

Division of Human Molecular Genetics, Research Center for Genetic Information, Medical Institute of Bioregulation, Kyushu University, and Fukuoka Prefectural Dazaifu Hospital Psychiatric Center, Fukuoka, Japan.

出版信息

Psychiatry Res. 2009 May 15;167(1-2):88-96. doi: 10.1016/j.psychres.2007.12.002. Epub 2009 Apr 7.

Abstract

Based on the hypothesis that a glutamatergic dysfunction is involved in the pathophysiology of schizophrenia, we have been conducting systematic studies on the association between glutamate receptor genes and schizophrenia. Here we report association studies of schizophrenia with polymorphisms in group III metabotropic glutamate receptor genes, GRM4 and GRM7. We selected 8 and 43 common SNPs distributed in the entire gene regions of GRM4 (>111 kb) and GRM7 (>900 kb), respectively. We scanned significant associations with schizophrenia using 100 case-control pairs of Japanese. We identified two neighboring SNPs (rs12491620 and rs1450099) in GRM7 showing highly significant haplotype association with schizophrenia surviving the FDR correction. We then performed additional typing of the two SNPs using the expanded sample set (404 cases and 420 controls) and confirmed the significant association with the disease. We conclude that at least one susceptibility locus for schizophrenia is located within or nearby GRM7, whereas GRM4 is unlikely to be a major susceptibility gene for schizophrenia in the Japanese population.

摘要

基于谷氨酸能功能障碍参与精神分裂症病理生理学的假说,我们一直在对谷氨酸受体基因与精神分裂症之间的关联进行系统研究。在此,我们报告精神分裂症与Ⅲ型代谢型谷氨酸受体基因GRM4和GRM7多态性的关联研究。我们分别选择了分布在GRM4(>111 kb)和GRM7(>900 kb)整个基因区域的8个和43个常见单核苷酸多态性(SNP)。我们使用100对日本病例对照对扫描了与精神分裂症的显著关联。我们在GRM7中鉴定出两个相邻的SNP(rs12491620和rs1450099),它们显示出与经FDR校正后仍与精神分裂症高度显著的单倍型关联。然后,我们使用扩大的样本集(404例病例和420例对照)对这两个SNP进行了额外分型,并证实了与该疾病的显著关联。我们得出结论,精神分裂症的至少一个易感位点位于GRM7内或其附近,而在日本人群中,GRM4不太可能是精神分裂症的主要易感基因。

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