首页> 外文期刊>American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics >Replication study and meta-analysis of the genetic association of GRM3 gene polymorphisms with schizophrenia in a large Japanese case-control population.
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Replication study and meta-analysis of the genetic association of GRM3 gene polymorphisms with schizophrenia in a large Japanese case-control population.

机译:在日本大量病例对照人群中,GRM3基因多态性与精神分裂症的遗传关联的复制研究和荟萃分析。

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摘要

The GRM3 gene, which encodes a metabotropic glutamate receptor, is an important candidate gene for susceptibility to schizophrenia. Two single nucleotide polymorphisms (SNPs), rs1468412 and rs2299225 in intron 3, were reported to be associated with schizophrenia in Japanese and Chinese populations, respectively. Haplotypes with these SNPs were also reported to be associated with schizophrenia. In the present study, we attempted to replicate these single marker and haplotype associations in a case-control study of 1,916 Japanese patients with schizophrenia and 1,915 Japanese control subjects. In addition to these two SNPs, we genotyped rs274622 in the promoter region of GRM3. In the present study, none of these polymorphisms were associated with schizophrenia (rs274622, allelic P = 0.68; rs1468412, allelic P = 0.74; rs2299225, allelic P = 0.20). Haplotypes constructed with these SNPs also were not associated with schizophrenia (P = 0.18-0.84). Meta-analysis of five case-control studies of more than 3,000 patients with schizophrenia and more than 3,000 control subjects did not support the associations of rs1468412 and rs2299225 with schizophrenia. Our data indicate that SNPs previously reported to be associated with schizophrenia do not contribute to genetic susceptibility to schizophrenia.
机译:编码代谢型谷氨酸受体的GRM3基因是对精神分裂症易感性的重要候选基因。内含子3中的两个单核苷酸多态性(SNP)rs1468412和rs2299225据报道分别与日本人和中国人的精神分裂症有关。据报道,具有这些SNP的单倍型与精神分裂症有关。在本研究中,我们试图在对1,916名日本精神分裂症患者和1,915名日本对照受试者的病例对照研究中复制这些单一标记和单倍型关联。除了这两个SNP,我们在GRM3的启动子区域对rs274622进行了基因分型。在本研究中,这些多态性均与精神分裂症无关(rs274622,等位基因P = 0.68; rs1468412,等位基因P = 0.74; rs2299225,等位基因P = 0.20)。用这些SNP构建的单倍型也与精神分裂症无关(P = 0.18-0.84)。对超过3,000名精神分裂症患者和超过3,000名对照受试者的五项病例对照研究的荟萃分析不支持rs1468412和rs2299225与精神分裂症的关联。我们的数据表明,以前报道与精神分裂症有关的SNP不会导致精神分裂症的遗传易感性。

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