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首页> 外文期刊>Chinese Medical Journal >Association of GYS1 and β_3-AR gene with postprandial hyperglycemia and serum uric acid in type 2 diabetes mellitus
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Association of GYS1 and β_3-AR gene with postprandial hyperglycemia and serum uric acid in type 2 diabetes mellitus

机译:GYS1和β_3-AR基因与2型糖尿病餐后高血糖和血尿酸的关系

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Objective To determine the relationships of Met416Val and Xbal polymorphism of muscle glycogen synthase (GYS1) gene and Trg64Arg variant of the β_3-adrenergic-receptor (β_3-AR) gene with type 2 diabetes mellitus (DM) and its intermediate phenotypes in the Chinese population. Methods Polymerase chain reaction-oligonucleotide ligation assay and restriction fragment length polymorphism assay were used to evaluate the GYS1 and β_3-AR gene polymorphisms in 102 pairs of case-control Chinese spouses. Results Subjects with Met416Val variant had a significantly higher 2-hour post-glucose level than subjects without this variant had in diabetic group (P = 0.032). The Met416Val polymorphism of GYS1 gene was not significantly associated with the risk of type 2 DM (adjusted OR = 1.67; 95% CI: 0.73 - 3.81, P = 0.223). Subjects with Trp64Arg variant had a significantly higher serum uric acid level than subjects without this variant had in diabetic group (P = 0.034). The combination of BMI and Arg64 allele carrier of the β_3-AR gene increased the diabetic risk over four-fold (adjusted OR = 4.00; 95% CI: 1.53 - 10.45, P = 0.005). Conclusions In the Chinese population, Met416Val polymorphism is identified in a subgroup of diabetic subjects with high 2-hour post-glucose. It will explain why some diabetic patients appear to be genetically predisposed to developing high postpradial glucose level. The presence of the Arg64 allele in the β_3-AR gene may predispose patients to higher serum uric acid level.
机译:目的探讨中国人群中糖原合酶(GYS1)基因的Met416Val和Xbal多态性以及β_3-肾上腺素能受体(β_3-AR)基因的Trg64Arg变异与2型糖尿病及其中间表型的关系。 。方法采用聚合酶链反应-寡核苷酸连接法和限制性片段长度多态性分析法对102对病例对照中国配偶的GYS1和β_3-AR基因多态性进行评估。结果与糖尿病组相比,具有Met416Val变异体的受试者的2小时葡萄糖后水平明显高于没有该变异体的受试者(P = 0.032)。 GYS1基因的Met416Val多态性与2型DM的风险没有显着相关(校正OR = 1.67; 95%CI:0.73-3.81,P = 0.223)。具有Trp64Arg变体的受试者的血清尿酸水平明显高于没有该变体的受试者的糖尿病组(P = 0.034)。 β_3-AR基因的BMI和Arg64等位基因携带者的组合使糖尿病风险增加了四倍(校正OR = 4.00; 95%CI:1.53-10.45,P = 0.005)。结论在中国人群中,Met416Val基因多态性存在于高血糖后2小时的糖尿病患者亚组中。这将解释为什么某些糖尿病患者在遗传上倾向于产生高p后葡萄糖水平。 β_3-AR基因中Arg64等位基因的存在可能使患者易患较高的血清尿酸水平。

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