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首页> 外文期刊>Translational research: the journal of laboratory and clinical medicine >Type 2 diabetes mellitus and its renal complications in relation to apolipoprotein E gene polymorphism.
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Type 2 diabetes mellitus and its renal complications in relation to apolipoprotein E gene polymorphism.

机译:2型糖尿病及其肾脏并发症与载脂蛋白E基因多态性的关系。

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The apolipoprotein E (APOE) epsilon2 allele is reported to be associated with greater risk of renal impairment in type 2 diabetes. Relationships among APOE polymorphisms, renal impairment, and biochemical parameters were explored. A prospective study of 405 consenting Chinese type 2 diabetic patients [mean age +/- standard deviation (SD): 59.2 +/- 10.3 years] without advanced complications at entry was conducted. APOE genotyping and measurement of plasma biomarkers of oxidative stress and antioxidants were performed at entry. HbA1C, plasma glucose, lipids, creatinine, urine albumin/creatinine, and blood pressure were measured at entry and at up to 4 years of follow-up. APOE allelic frequencies were in Hardy-Weinberg equilibrium. Odds ratios of albuminuria at entry and/or during follow-up for different APOE groups were not significantly different. The non-epsilon2 (epsilon3/3, epsilon3/4, epsilon4/4) group had significantly greater plasma ascorbate (51.6 +/- 20.1 mumol/L) than the epsilon2 (epsilon2/2, epsilon2/3) group (44.5 +/- 16.2 mumol/L, P = 0.021), but higher plasma ascorbate levels did not seem to decrease the risk of renal impairment in the non-epsilon2 group. Baseline plasma lipid-standardized alpha-tocopherol levels were least in epsilon2 subjects with persistent albuminuria (3.6 +/- 1.1 mumol/mmol of total cholesterol plus triglycerides, P = 0.008) compared with epsilon2 subjects who had no albuminuria at entry or during follow-up (4.5 +/- 0.8 mumol/mmol of total cholesterol plus triglycerides). The APOE epsilon2 allele does not seem to be associated with increased risk of renal impairment in Chinese type 2 diabetic patients. Plasma lipid-standardized alpha-tocopherol may play a role in determining risk of renal dysfunction in type 2 diabetes.
机译:据报道,载脂蛋白E(APOE)epsilon2等位基因与2型糖尿病肾损害的更大风险相关。探索了APOE基因多态性,肾功能不全和生化参数之间的关系。一项前瞻性研究纳入了405名同意接受治疗的中国2型糖尿病患者[平均年龄+/-标准差(SD):59.2 +/- 10.3年],这些患者在进入时并未出现严重并发症。进入时进行了APOE基因分型,并测定了氧化应激和抗氧化剂的血浆生物标志物。在入院时和长达4年的随访中测量HbA1C,血糖,血脂,肌酐,尿白蛋白/肌酐和血压。 APOE等位基因频率处于Hardy-Weinberg平衡状态。不同APOE组在进入和/或随访期间蛋白尿的几率没有显着差异。非epsilon2(epsilon3 / 3,epsilon3 / 4,epsilon4 / 4)组的血浆抗坏血酸(51.6 +/- 20.1 mumol / L)比epsilon2(epsilon2 / 2,epsilon2 / 3)组(44.5 + / -16.2 mumol / L,P = 0.021),但较高的血浆抗坏血酸水平似乎并未降低非epsilon2组肾脏损害的风险。相较于进入或随访期间无蛋白尿的epsilon2受试者,基线持续的蛋白尿水平为标准化的血浆脂质标准化的α-生育酚水平最低(3.6 +/- 1.1μmol/ mmol总胆固醇加甘油三酯,P = 0.008)。 (总胆固醇加甘油三酸酯为4.5 +/- 0.8摩尔/毫摩尔)。在中国2型糖尿病患者中,APOE epsilon2等位基因似乎与肾功能损害的风险增加无关。血浆脂质标准化的α-生育酚可能在确定2型糖尿病肾功能不全的风险中起作用。

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