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首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Platelet collagen receptor alpha2beta1 integrin and glycoprotein IIIa Pl(A1/A2) polymorphisms are not associated with nephropathy in type 2 diabetes.
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Platelet collagen receptor alpha2beta1 integrin and glycoprotein IIIa Pl(A1/A2) polymorphisms are not associated with nephropathy in type 2 diabetes.

机译:血小板胶原蛋白受体α2β1整合素和糖蛋白IIIa P1(A1 / A2)多态性与2型糖尿病的肾病无关。

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Platelet glycoprotein receptors play a role in the pathogenesis of chronic diabetic complications. Genetic polymorphisms of the alpha2beta1 integrin and glycoprotein IIIa (GPIIIa) have been associated with myocardial infarction, stroke, and diabetic retinopathy. To identify risk factors for their development in a cohort of patients with type 2 diabetes, we evaluated clinical variables and genetic polymorphisms in the alpha2beta1 integrin and GPIIIa genes. Two hundred thirty-four subjects with type 2 diabetes (126 patients with and 108 patients without diabetic nephropathy), as well as 217 nondiabetic healthy subjects, were recruited for this study. Clinical factors for investigation included sex, age at diagnosis, duration of diabetes, body mass index (BMI), and fasting plasma glucose, hemoglobin A(1c) (HbA(1c)), total cholesterol, and triglyceride levels. Genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism analyses. No difference in the Bgl II polymorphism of the alpha2beta1 integrin gene was found between patients with type 2 diabetes with or without nephropathy (11 [8.7%], 47 [37.3%], and 68 patients [54.0%] versus 10 [9.3%], 32 [29.6%], and 66 patients [61.1%] for Bgl II+/+, Bgl II+/-, and Bgl II-/-, respectively; P = 0.271). Multiple logistic regression analyses showed that duration of diabetes, BMI, hypertension, and poor glycemic control were four independent predictors for the development of diabetic nephropathy. No contribution of the Bgl II+ allele of the alpha2beta1 integrin was found for the risk for nephropathy (odds ratio, 1.258; 95% confidence interval, 0.655 to 2.418; P = 0.490). The Pl(A2) allele genotype was not found among our studied subjects. In conclusion, age, duration of diabetes, BMI, and HbA(1c) level are strong predictors for nephropathy in patients with type 2 diabetes. However, the Bgl II polymorphism of the alpha2beta1 integrin gene and the Apa I polymorphism of the platelet GPIIIa gene do not have a major role in the development of diabetic nephropathy in our population.
机译:血小板糖蛋白受体在慢性糖尿病并发症的发病机理中起作用。 alpha2beta1整合素和糖蛋白IIIa(GPIIIa)的遗传多态性已与心肌梗塞,中风和糖尿病性视网膜病变相关。为了确定在一组2型糖尿病患者中其发展的危险因素,我们评估了alpha2beta1整合素和GPIIIa基因的临床变量和遗传多态性。招募了234名2型糖尿病受试者(126名患有糖尿病和108名无糖尿病肾病的患者)以及217名非糖尿病健康受试者。调查的临床因素包括性别,诊断年龄,糖尿病持续时间,体重指数(BMI)和空腹血糖,血红蛋白A(1c)(HbA(1c)),总胆固醇和甘油三酸酯水平。通过聚合酶链反应和限制性片段长度多态性分析确定基因型。在患有或不患有肾病的2型糖尿病患者之间,没有发现alpha2beta1整合素基因的Bgl II多态性差异(11 [8.7%],47 [37.3%]和68患者[54.0%]对10 [9.3%]) Bgl II + / +,Bgl II +/-和Bgl II-/-分别为32例[29.6%]和66例[61.1%]; P = 0.271)。多项逻辑回归分析表明,糖尿病持续时间,BMI,高血压和血糖控制不佳是糖尿病肾病发展的四个独立预测因子。没有发现α2β1整联蛋白的Bgl II +等位基因对患肾病的风险有贡献(优势比为1.258; 95%置信区间为0.655至2.418; P = 0.490)。在我们研究的受试者中未发现P1(A2)等位基因基因型。总之,年龄,糖尿病持续时间,BMI和HbA(1c)水平是2型糖尿病患者肾病的重要预测指标。但是,α2beta1整合素基因的Bgl II多态性和血小板GPIIIa基因的Apa I多态性在我们人群中糖尿病肾病的发生中没有主要作用。

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