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首页> 外文期刊>International Journal of General Medicine >Association of GSTP1 , GSTT1 and GSTM1 Gene Variants with Coronary Artery Disease in Iranian Population: A Case–Control Study
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Association of GSTP1 , GSTT1 and GSTM1 Gene Variants with Coronary Artery Disease in Iranian Population: A Case–Control Study

机译:GSTP1,GSTT1和GSTM1基因变种与伊朗人群冠状动脉疾病的基因变异性:一个案例对照研究

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Background: Coronary artery disease (CAD) is a multifactorial disease that may be caused by the interaction between environmental and genetic risk factors. Glutathione S-transferases (GSTs) are known to participate in detoxification and metabolism of a wide range of xenobiotic compounds and oxidative stress products. Considering the interaction between environmental and genetic factors in CAD, we investigated the genetic polymorphisms of GSTM1, GSTT1 , and GSTP1 in the Iranian population. Patients and Methods: Two hundred and forty-four CAD cases and 281 healthy controls were studied. The genotype of GSTM1, GSTT1 , and GSTP1 genes was determined by multiplex polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (PCR-RFLP) techniques. Multivariable logistic regression analysis was used to calculate the odds ratios (ORs) and 95% confidence intervals (CI). Multifactor dimensionality reduction (MDR) analysis was also carried out to analyze the gene–gene and gene–environment interaction. Results: The genotype and allele distribution of the three variations were not significantly different between CAD patients and controls (p 0.05). The subgroup analysis revealed no significant gene–gene interactions or gene–gene combination effects linked to CAD susceptibility. However, MDR analysis selected the GSTM, GSTT pairwise and three genes combination models associated with the susceptibility to CAD. In addition, its result revealed that smoking in combination with GSTM1 (two-way) and GSTT, GSTP (three-way) genes might increase the risk of CAD. Furthermore, a significant interaction between GSTT1 -null polymorphism and dyslipidemia was found in multivariable logistic regression analyses in the gene–environmental interactions on CAD risk. Conclusion: Our results suggest that the GSTM1, GSTT1 and GSTP1 genetic variations are not directly associated with the susceptibility to CAD in Iranian patients. Due to MDR results, there might be a non-linear association between interactions of two or three genes and smoking with CAD. There is also an association between CAD risk factors and GST variations, which requires supplementary confirmation with larger sample sizes.
机译:背景:冠状动脉疾病(CAD)是一种多因素疾病,可能是由环境和遗传危险因素之间的相互作用引起的。已知谷胱甘肽S-转移酶(GSTS)参与广泛的十二生素化合物和氧化应激产物的解毒和代谢。考虑到CAD中环境和遗传因素之间的相互作用,我们研究了伊朗人群的GSTM1,GSTT1和GSTP1的遗传多态性。患者和方法:研究了两百四十四例,研究了281例健康对照。通过多重聚合酶链反应(PCR限制片段长度多态性(PCR-RFLP)技术,测定GSTM1,GSTT1和GSTP1基因的基因型。多变量逻辑回归分析用于计算大量比率(或)和95%置信区间(CI)。还进行了多因素维度降低(MDR)分析以分析基因基因和基因环境相互作用。结果:CAD患者和对照之间的三种变异的基因型和等位基因分布(P> 0.05)没有显着差异。亚组分析显示没有显着的基因相互作用或与CAD易感性相关的基因基因组合效应。然而,MDR分析选择了与CAD易感性相关的GSTM,GSTT成对和三个基因组合模型。此外,其结果显示,与GSTM1(双向)和GSTT组合吸烟,GSTP(三向)基因可能会增加CAD的风险。此外,在CAD风险的基因 - 环境相互作用中的多变量逻辑回归分析中发现了GSTT1-unull多态性和血脂过度血症之间的显着相互作用。结论:我们的研究结果表明,GSTM1,GSTT1和GSTP1遗传变异与伊朗患者的CAD易感性没有直接相关。由于MDR结果,两种或三种基因的相互作用与CAD吸烟可能存在非线性关联。 CAD风险因素和GST变化之间还存在关联,这需要补充的样本尺寸的补充确认。

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