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伊朗南部谷胱甘肽 S-转移酶(GSTM1、GSTT1、GSTP1)多态性与 2 型糖尿病的相关性研究。

Study of the association between glutathione S-transferase (GSTM1, GSTT1, GSTP1) polymorphisms with type II diabetes mellitus in southern of Iran.

机构信息

Department of Genetics, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran.

出版信息

Mol Biol Rep. 2012 Dec;39(12):10187-92. doi: 10.1007/s11033-012-1893-4. Epub 2012 Sep 27.

Abstract

Diabetes Mellitus is characterized by chronic hyperglycemia and associated with an increased production of reactive oxygen species (ROS). Oxidative stress is the result of accumulation of free radicals in tissues which specially affects beta cells in pancreas. Glutathione S-transferases (GSTs) are a family of antioxidant enzymes that include several classes of GSTs. These enzymes have important roles in decreasing of ROS species and act as a kind of antioxidant defense. To investigate the association between GSTs polymorphism with type 2 diabetes mellitus (T2DM), we investigated the frequency of GSTM1, T1 and P1 genotypes in patients with T2DM and controls. The genotypes of GSTT1, M1 and P1 were determined in 171 clinically documented T2DM patients and 169 normal cases (as controls) by multiplex polymerase chain reaction and PCR-RFLP. In diabetic patients, the frequency of GSTM1-null genotype was significantly (OR = 1.74; 95 % CI = 1.13-2.69, P = 0.016) higher than that in control. However, the frequency of GSTT1 (OR = 1.29; 95 % CI = 0.07-2.14, P = 0.367) and GSTP1 (OR = 0.83; 95 % CI = 0.53-1.30, P = 0.389) genotypes were not significantly different comparing both groups. Also, the frequency of both GSTT1-null and GSTM1-null genotypes in patients (19.88 %) was significantly higher compared to controls with the same genotypes (11.83 %, P = 0.022). Our results indicated that GSTM1 and GSTT1 genotypes might be involved in the pathogenesis of T2DM in south Iranian population.

摘要

糖尿病的特征是慢性高血糖,与活性氧(ROS)的产生增加有关。氧化应激是自由基在组织中积累的结果,特别是影响胰腺中的β细胞。谷胱甘肽 S-转移酶(GSTs)是抗氧化酶家族,包括几类 GSTs。这些酶在减少 ROS 方面具有重要作用,并作为一种抗氧化防御。为了研究 GSTs 多态性与 2 型糖尿病(T2DM)之间的关系,我们研究了 T2DM 患者和对照组中 GSTM1、T1 和 P1 基因型的频率。通过多重聚合酶链反应和 PCR-RFLP 确定了 171 例临床记录的 T2DM 患者和 169 例正常病例(作为对照)的 GSTT1、M1 和 P1 基因型。在糖尿病患者中,GSTM1 缺失基因型的频率明显升高(OR = 1.74;95%CI = 1.13-2.69,P = 0.016)高于对照组。然而,GSTT1(OR = 1.29;95%CI = 0.07-2.14,P = 0.367)和 GSTP1(OR = 0.83;95%CI = 0.53-1.30,P = 0.389)基因型的频率在两组之间没有显著差异。此外,患者中 GSTT1 缺失和 GSTM1 缺失基因型的频率(19.88%)明显高于对照组中具有相同基因型的患者(11.83%,P = 0.022)。我们的结果表明,GSTM1 和 GSTT1 基因型可能参与了伊朗南部人群 T2DM 的发病机制。

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