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伊朗人群样本中谷胱甘肽S-转移酶基因多态性与精神分裂症风险的分析。

Analysis of glutathione S-transferase genes polymorphisms and the risk of schizophrenia in a sample of Iranian population.

作者信息

Kashani Farah Lotfi, Kordi-Tamandani Dor Mohammad, Sahranavard Roya, Hashemi Mohammad, Kordi-Tamandani Farzaneh, Torkamanzehi Adam

机构信息

Department of Clinical Psychology, Islamic Azad University Roudehen Branch, Roudehen, Iran.

出版信息

Neuron Glia Biol. 2011 May;7(2-4):199-203. doi: 10.1017/S1740925X12000130. Epub 2012 Jul 6.

DOI:10.1017/S1740925X12000130
PMID:22874804
Abstract

Glutathione S-transferases (GSTs) are major intracellular antioxidants, which, impaired in their function, are involved in the progress of schizophrenia (SCZ). The aim of this case-control study was to investigate the association between the polymorphism of glutathione S-transferases M1 (GSTM1), T1 (GSTT1), the glutathione S-transferase P1 gene (GSTP1) and SCZ. We isolated genomic DNA from peripheral blood of 93 individuals with SCZ and 99 healthy control subjects' genotypes analyzing them for GSTM1, GSTT1 and GSTP1 using polymerase chain reaction. The analysis of the gene-gene interaction between GSTs indicated that the magnitude of the association was greater for the combined AG/GSTT1 & GSTM1 genotypes (OR = 2.51; 95% CI: 1.13-5.63, P = 0.02). The AG and combined AG + GG genotypes of GSTP1 increased the risk of SCZ (OR = 1.83; 95% CI: 0.94-3.75 and OR = 1.71; 95% CI: 0.92-3.19, respectively). The genotypes of GSTT/NULL, NULL/GSTM and NULL/NULL increased the risk of SCZ (OR = 2.05; 95% CI: 0.9-4.74; OR = 2.0; 95% CI: 1.68-2.31; and OR = 1.8; 95% CI: 0.57-2.46, respectively). The present study supports previous data that suggest that impairment in the function of GSTs genes may increase the risk of SCZ.

摘要

谷胱甘肽S-转移酶(GSTs)是主要的细胞内抗氧化剂,其功能受损与精神分裂症(SCZ)的进展有关。本病例对照研究的目的是调查谷胱甘肽S-转移酶M1(GSTM1)、T1(GSTT1)、谷胱甘肽S-转移酶P1基因(GSTP1)的多态性与SCZ之间的关联。我们从93例SCZ患者的外周血中分离基因组DNA,并从99名健康对照者中分离基因组DNA,采用聚合酶链反应对它们进行GSTM1、GSTT1和GSTP1基因分型分析。GSTs基因间相互作用的分析表明,AG/GSTT1与GSTM1联合基因型的关联程度更大(比值比=2.51;95%置信区间:1.13 - 5.63,P = 0.02)。GSTP1的AG及AG + GG联合基因型增加了SCZ的发病风险(比值比分别为1.83;95%置信区间:0.94 - 3.75和1.71;95%置信区间:0.92 - 3.19)。GSTT/NULL、NULL/GSTM和NULL/NULL基因型增加了SCZ的发病风险(比值比分别为2.05;95%置信区间:0.9 - 4.74;2.0;95%置信区间:1.68 - 2.31;1.8;95%置信区间:0.57 - 2.46)。本研究支持先前的数据,即GSTs基因功能受损可能增加SCZ的发病风险。

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