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在一项针对汉族人群的复制研究中,MPC2 变体与精神分裂症之间缺乏关联。

Lack of association between MPC2 variants and schizophrenia in a replication study of Han Chinese.

机构信息

Wuxi Mental Health Center, Wuxi 214151, Jiangsu Province, China.

出版信息

Neurosci Lett. 2013 Sep 27;552:120-3. doi: 10.1016/j.neulet.2013.07.051. Epub 2013 Aug 8.

DOI:10.1016/j.neulet.2013.07.051
PMID:23933155
Abstract

Schizophrenia (SCZ) is a common, complex and severe psychiatric disorder associated with many different risk factors, both genetic and environmental. A recent genome-wide association study (GWAS) of Han Chinese identified a single-nucleotide polymorphism (SNP, rs10489202) in the mitochondrial pyruvate carrier 2 gene (MPC2, also known as BRP44) as a possible susceptibility locus for schizophrenia. Hoping to validate this finding, we conducted a case-control study of Han Chinese with 1093 schizophrenia cases and 1022 healthy controls, using the LDR-PCR method to genotype polymorphisms (rs10489202 and a TagSNP rs203861) in the MPC2 gene. However, we found no significant difference (P>0.05) in either allele or genotype frequency in the SNPs between patients and controls. These results did not support the previous finding suggesting the further study by using a large-scale association analysis in the future should be warranted in Han Chinese populations.

摘要

精神分裂症(SCZ)是一种常见的、复杂的和严重的精神疾病,与许多不同的遗传和环境风险因素有关。最近一项针对汉族人的全基因组关联研究(GWAS)发现,线粒体丙酮酸载体 2 基因(MPC2,也称为 BRP44)中的单核苷酸多态性(SNP,rs10489202)可能是精神分裂症的易感基因座。为了验证这一发现,我们对 1093 例精神分裂症患者和 1022 例健康对照进行了一项汉族人的病例对照研究,采用 LDR-PCR 方法对 MPC2 基因中的多态性(rs10489202 和 TagSNP rs203861)进行基因分型。然而,我们在患者和对照组之间的 SNPs 中未发现等位基因或基因型频率有显著差异(P>0.05)。这些结果不支持先前的发现,提示未来在汉族人群中应进行大规模关联分析以进一步研究。

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Common variants on 17q25 and gene-gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain.
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