肿瘤坏死因子- α和IV型胶原蛋白对2型糖尿病肾病的诊断价值

Mohamed Omran, Anhar Elmetwaly, T. Emran, A. Eldeeb, A. Belal, F. Mohamed
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摘要

背景:糖尿病肾病是1型和2型糖尿病的严重并发症。它也被称为糖尿病肾病(DKD)。在美国,大约三分之一的糖尿病患者患有糖尿病肾病。这就需要找到更好的生物标志物来诊断糖尿病肾病。该研究旨在评估肿瘤坏死因子α (TNFα)和IV型胶原作为2型糖尿病患者糖尿病肾病及其进展检测的潜在生物标志物。材料与方法:本横断面研究共纳入88名受试者。患者分为三大类;糖尿病合并DKD组(n=50),非糖尿病合并DKD组(n=28),健康对照组(n=10)。测量所有受试者的TNFα和IV型胶原蛋白水平。采用受试者工作特征下面积(AUC)评价单一及联合TNFα和IV型胶原的诊断价值。结果:对于糖尿病患者与健康人群的区分,最有效的标志物是TNF-α (AUC= 0.81,敏感性70%,特异性70%)。对于区分患有DKD的糖尿病患者和不患有DKD的糖尿病患者,最有效的标志物是IV型胶原蛋白(AUC= 0.77,敏感性69%,特异性73%)。有趣的是,我们基于两种血液标志物(TNF-α和IV型胶原)开发了一种区分DM和DM- dkd的新指标。发达指数的AUC为0.93;有DKD的糖尿病与无DKD的糖尿病的区分率为0.79。与健康个体区分早期DKD的发育指数AUC为0.90。鉴别DM患者早期和晚期DKD的发达指数AUC为0.83。结论:TNFα和IV型胶原蛋白可能对早期发现和区分DKD糖尿病和非DKD糖尿病有潜在的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic performances of tumor necrosis factor-alpha and type IV collagen for diabetic nephropathy in type 2 diabetic patients
Background : Diabetic nephropathy is a serious complication of both type 1 and type 2 diabetes. It's also called diabetic kidney disease (DKD). In the United States, about 1 in 3 people with diabetes have diabetic nephropathy. This necessitates identifying better biomarkers that diagnose diabetic nephropathy. The study aimed to evaluate tumor necrosis factor α (TNFα) and type IV collagen as potential biomarkers for the detection of diabetic nephropathy and its progression in patients with type 2 diabetes. Materials and Methods: A total of 88 subjects were included in this cross-sectional study. Patients were classified into three major groups; diabetics with DKD group (n=50), diabetics without DKD group (n=28), and healthy control group (n=10). TNFα and type IV collagen levels were measured in all subjects. The diagnostic value of single and combined TNFα and type IV collagen was assessed by the area under the receiver operating characteristic (AUC). Results: For discrimination between diabetics with DKD from healthy individuals, the most efficient marker was TNF-α (AUC= 0.81, 70% sensitivity, and 70% specificity. For discriminant between DM patients with DKD from DM patients without DKD, the most efficient marker was type IV collagen (AUC= 0.77, 69% sensitivity, and 73% specificity. Interestingly, we developed a new index for differentiating between DM and DM-DKD based on two blood markers (TNF-α and type IV collagen). The AUC of the developed index was 0.93; 0.79 for discriminated DM with DKD from DM without DKD. The AUC of the developed index was 0.90 for discriminated early DKD from healthy individuals. Also, The AUC of the developed index was 0.83 for discrimination early from late DKD among DM patients. Conclusions: TNFα and type IV collagen may be potentially useful for early detection and to discriminate diabetics with DKD from DM without DKD.
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