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谷胱甘肽过氧化物酶1(GPX1)Pro198Leu多态性和谷胱甘肽S-转移酶P1(GSTP1)Ile105Val多态性与中国汉族人群精神分裂症风险无关。

GPX1 Pro198Leu polymorphism and GSTP1 Ile105Val polymorphisms are not associated with the risk of schizophrenia in the Chinese Han population.

作者信息

Gao Huijie, Liu Chao, Song Sijia, Zhang Chuanqiang, Ma Qun, Li Xiao, Xu Luo

机构信息

aDepartment of Pathophysiology, Medical College of Qingdao University, Qingdao bDepartment of Basic Medicine, College of Pharmacy, Jining Medical University cRizhao Mental Health Center dDepartment of Neurosurgery, Rizhao Hospital of Traditional Chinese Medicine eFoundation College of Jining Medical University, Jining, China.

出版信息

Neuroreport. 2017 Oct 18;28(15):969-972. doi: 10.1097/WNR.0000000000000870.

Abstract

Increasing lines of evidence show that oxidative stress plays a role in the pathophysiological mechanisms of schizophrenia (SCZ). Polymorphic variants of oxidative stress-related candidate genes GPX1 and GST1 can affect the antioxidant activities of their encoded enzymes. Therefore, this study aimed to explore the association between the single nucleotide polymorphisms (SNPs) of GPX1 and GSTP1 and susceptibility to schizophrenia in the Chinese Han population. DNA from 323 healthy controls and 210 schizophrenic patients was genotyped for SNPs rs1050450 in GPX1 and rs1695 in GSTP1 using a predesigned TaqMan SNP genotyping assay. Differences in genetic distributions between cases and controls were compared using the χ-test. No significant differences in allelic or genotypic frequencies of GPX1 rs1050450 or GSTP1 rs1695 were detected between cases and controls (GPX1 rs1050450: χ=0.370, P=0.831 by genotype, χ=0.377, P=0.539, odds ratio=1.145, 95% confidence interval=0.743-1.766 by allele; GSTP1 rs1695: χ=1.537, P=0.464 by genotype, χ=1.623, P=0.203, odds ratio=0.813, 95% confidence interval=0.592-1.118 by allele). Our results suggest that GPX1 rs1050450 and GSTP1 rs1695 SNPs are unlikely to play a major role in the pathogenesis of schizophrenia in the Chinese Han population. However, these results should be validated by replication in larger and independent samples.

摘要

越来越多的证据表明,氧化应激在精神分裂症(SCZ)的病理生理机制中发挥作用。氧化应激相关候选基因GPX1和GST1的多态性变异可影响其编码酶的抗氧化活性。因此,本研究旨在探讨中国汉族人群中GPX1和GSTP1的单核苷酸多态性(SNP)与精神分裂症易感性之间的关联。使用预先设计的TaqMan SNP基因分型检测法,对323名健康对照者和210名精神分裂症患者的DNA进行GPX1基因rs1050450和GSTP1基因rs1695的基因分型。采用χ检验比较病例组和对照组之间的基因分布差异。病例组和对照组之间未检测到GPX1 rs1050450或GSTP1 rs1695的等位基因或基因型频率有显著差异(GPX1 rs1050450:基因型χ=0.370,P=0.831;等位基因χ=0.377,P=0.539,比值比=1.145,95%置信区间=0.743-1.766;GSTP1 rs1695:基因型χ=1.537,P=0.464;等位基因χ=1.623,P=0.203,比值比=0.813,95%置信区间=0.592-1.118)。我们的结果表明,GPX1 rs1050450和GSTP1 rs1695 SNP不太可能在中国汉族人群精神分裂症的发病机制中起主要作用。然而,这些结果应在更大规模的独立样本中进行重复验证。

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