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GSTO2*N142D 基因多态性与意大利患者的甲状腺功能减退症相关。

GSTO2*N142D gene polymorphism associated with hypothyroidism in Italian patients.

机构信息

Department of Biology, University of Rome "Tor Vergata", Via della Ricerca Scientifica 1, 00133, Rome, Italy.

出版信息

Mol Biol Rep. 2013 Feb;40(2):1967-71. doi: 10.1007/s11033-012-2253-0. Epub 2012 Oct 19.

Abstract

Hypothyroidism is a multifactorial endocrinal disease characterized by abnormally low thyroid hormone production. Thyroiditis is one of the primary causes of hypothyroidism, as it is an increasing level of inflammation in the thyroid gland that could be due to a failure of the anti-inflammatory response. Glutathione S-transferases are biomarkers of inflammation and oxidative stress. These phase II enzymes play a relevant role in detoxifying xenobiotic compounds. Particular attention has been focused on GSTA1, GSTM1, GSTO2, GSTP1, and GSTT1 genes to evaluate if GST gene polymorphisms are associated with hypothyroidism. We screened a case-control population (patients with hypothyroidism n = 110, controls n = 122) to analyze GST gene polymorphisms. GST SNPs were determined using the PCR-RFLP method, while GST null polymorphisms were determined using a Multiplex PCR. In this study, we found differences in genotype distribution between hypothyroid individuals and controls only for the GSTO2*N142D polymorphism. Logistic regression analysis, after adjustment for age and sex, confirmed this positive association (OR = 4.56; 95 % CI 1.22-17.00; p = 0.009). The GSTO2 enzyme can catalyze several reactions important for countering oxidative stress: subjects with the D142 allele may have a deficiency in the antioxidant enzymatic system. A decrease in antioxidant capacity may trigger increased oxidative stress. Previous studies have highlighted the role of GST enzymes in inflammation disorders, but no data are available on their role in hypothyroidism. Our results suggest that GSTO2 could increase disease risk susceptibility and could act as a risk factor for hypothyroidism in Italian patients.

摘要

甲状腺功能减退症是一种多因素内分泌疾病,其特征是甲状腺激素产生异常低。甲状腺炎是甲状腺功能减退症的主要原因之一,因为它是甲状腺中炎症水平升高,可能是由于抗炎反应失败。谷胱甘肽 S-转移酶是炎症和氧化应激的生物标志物。这些 II 相酶在解毒外来化合物方面发挥着重要作用。人们特别关注 GSTA1、GSTM1、GSTO2、GSTP1 和 GSTT1 基因,以评估 GST 基因多态性是否与甲状腺功能减退症有关。我们筛选了病例对照人群(甲状腺功能减退症患者 n=110,对照组 n=122)来分析 GST 基因多态性。使用 PCR-RFLP 方法确定 GST SNPs,使用多重 PCR 确定 GST 无效多态性。在这项研究中,我们仅发现 GSTO2*N142D 多态性在甲状腺功能减退个体和对照组之间的基因型分布存在差异。在调整年龄和性别后,逻辑回归分析证实了这种正相关(OR=4.56;95%CI 1.22-17.00;p=0.009)。GSTO2 酶可以催化几种对抗氧化应激很重要的反应:携带 D142 等位基因的个体可能缺乏抗氧化酶系统。抗氧化能力的下降可能会引发氧化应激增加。先前的研究强调了 GST 酶在炎症性疾病中的作用,但尚无关于其在甲状腺功能减退症中的作用的数据。我们的结果表明,GSTO2 可能会增加疾病风险易感性,并可能成为意大利患者甲状腺功能减退症的一个危险因素。

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