Yang Lina, Li Hongyan, Yu Ting, Zhao Haijun, Cherian M George, Cai Lu, Liu Ya
School of Public Health, Jilin University, Changchun, China.
Am J Physiol Endocrinol Metab. 2008 May;294(5):E987-92. doi: 10.1152/ajpendo.90234.2008. Epub 2008 Mar 18.
Metallothionein (MT) as a potent antioxidant can affect energy metabolism. The present study was undertaken to investigate the association between MT gene polymorphism and type 2 diabetes mellitus. Using the PCR-based restriction fragment length polymorphism method, seven single nucleotide polymorphisms (SNPs) in MT genes (rs8052394 and rs11076161 in MT1A gene, rs8052334, rs964372, and rs7191779 in MT1B gene, rs708274 in MT1E gene, and rs10636 in MT2A gene) were detected in 851 Chinese people of Han descent (397 diabetes and 454 controls). Several serum measurements were also examined randomly for 43 diabetic patients and 41 controls. The frequency distributions of the G allele in SNP rs8052394 of MT1A gene were significantly associated with the incidence of type 2 diabetes. There was no difference between patients and controls for the rest of six SNPs. Serum levels of interleukin-6 and tumor necrosis factor-alpha were higher, and serum superoxide dismutase activity was significantly lower in the diabetic group than those in the control group. For diabetic patients, serum superoxide dismutase activity was significantly lower in GG or GA carriers than those of AA carriers of rs8052394 SNP. Increased serum levels in diabetic patients were positively associated with rs964372 SNP, and type 2 diabetes with neuropathy was positively associated with rs10636 and rs11076161. These results suggest that multiple SNPs in MT genes are associated with diabetes and its clinical symptoms. Furthermore, MT1A gene in rs8052394 SNP is most likely the predisposition gene locus for diabetes or changes of serum superoxide dismutase activity.
金属硫蛋白(MT)作为一种强效抗氧化剂,可影响能量代谢。本研究旨在探讨MT基因多态性与2型糖尿病之间的关联。采用基于聚合酶链反应的限制性片段长度多态性方法,在851名汉族中国人(397例糖尿病患者和454例对照)中检测了MT基因中的7个单核苷酸多态性(SNP)(MT1A基因中的rs8052394和rs11076161、MT1B基因中的rs8052334、rs964372和rs7191779、MT1E基因中的rs708274以及MT2A基因中的rs10636)。还随机对43例糖尿病患者和41例对照进行了多项血清检测。MT1A基因SNP rs8052394中G等位基因的频率分布与2型糖尿病的发病率显著相关。其余6个SNP在患者和对照之间没有差异。糖尿病组血清白细胞介素-6和肿瘤坏死因子-α水平较高,血清超氧化物歧化酶活性显著低于对照组。对于糖尿病患者,rs8052394 SNP的GG或GA携带者血清超氧化物歧化酶活性显著低于AA携带者。糖尿病患者血清水平升高与rs964372 SNP呈正相关,2型糖尿病合并神经病变与rs10636和rs11076161呈正相关。这些结果表明,MT基因中的多个SNP与糖尿病及其临床症状相关。此外,rs8052394 SNP中的MT1A基因很可能是糖尿病或血清超氧化物歧化酶活性变化的易感基因位点。