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意大利哮喘患者 GSTA1、GSTO1 和 GSTO2 基因多态性。

GSTA1, GSTO1 and GSTO2 gene polymorphisms in Italian asthma patients.

机构信息

Department of Biology, University of Rome Tor Vergata, Rome, Italy.

出版信息

Clin Exp Pharmacol Physiol. 2010 Aug;37(8):870-2. doi: 10.1111/j.1440-1681.2010.05385.x. Epub 2010 Mar 30.

DOI:10.1111/j.1440-1681.2010.05385.x
PMID:20374258
Abstract
  1. Previous studies have established that genetic alterations in glutathione S-transferase enzymes may change the ability of the airway to deal with toxic substances and increase the risk of asthma. The present study analysed the association between asthma and GSTA1, GSTO1 and GSTO2 gene polymorphisms. 2. The GSTA1*-69C/T, GSTO1A140D and GSTO2N142D polymorphisms were detected by polymerase chain reaction-restriction fragment length polymorphism, whereas the GSTO1E155del polymorphism was detected using the confronting two-pair primer method. 3. Distribution of the GSTA1-69C/T genotype differed significantly between asthmatics and controls. Subjects with at least one allele -69T in the GSTA1 genotype have an increased risk of asthma (odds ratio (OR) 3.45; 95% confidence interval (CI) 1.80-6.62). The distribution of the GSTO1 genotype was nearly equal between the control group and asthmatics, however, the distribution of the GSTO2 gene differed significantly between asthmatics and controls (Chi-squared test). Subjects who had the GSTO2 homozygous D142 genotype were found to have an increased risk of asthma (OR 5.91; 95% CI 1.80-19.42). 4. The results show a potential association between the GST genes and asthma. This is particularly significant given that, in the literature, there are no epidemiological studies on alpha and omega classes of glutathione transferases in asthma.
摘要
  1. 先前的研究已经证实,谷胱甘肽 S-转移酶基因的遗传改变可能会改变气道处理有毒物质的能力,并增加哮喘的风险。本研究分析了 GSTA1、GSTO1 和 GSTO2 基因多态性与哮喘之间的关联。

  2. 通过聚合酶链反应-限制性片段长度多态性检测 GSTA1*-69C/T、GSTO1A140D 和 GSTO2N142D 多态性,而 GSTO1*E155del 多态性则使用对比两对引物方法进行检测。

  3. GSTA1*-69C/T 基因型的分布在哮喘患者和对照组之间存在显著差异。GSTA1 基因型中至少有一个 -69T 等位基因的个体患哮喘的风险增加(比值比 (OR) 3.45;95%置信区间 (CI) 1.80-6.62)。GSTO1 基因型在对照组和哮喘患者之间的分布几乎相等,然而 GSTO2 基因的分布在哮喘患者和对照组之间存在显著差异(卡方检验)。具有 GSTO2 纯合子 D142 基因型的个体被发现患哮喘的风险增加(OR 5.91;95% CI 1.80-19.42)。

  4. 研究结果表明 GST 基因与哮喘之间存在潜在的关联。鉴于文献中尚无关于 alpha 和 omega 类谷胱甘肽转移酶在哮喘中的流行病学研究,这一点尤其重要。

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