血清hcy、血清cys、尿微量白蛋白联合检测对2型糖尿病合并早期糖尿病肾病的诊断价值。

ISRN endocrinology Pub Date : 2013-09-18 eCollection Date: 2013-01-01 DOI:10.1155/2013/407452
Tengkai Wang, Qian Wang, Zhimei Wang, Zuomin Xiao, Lunqin Liu
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引用次数: 28

摘要

糖尿病肾病(DN)是终末期肾脏疾病的主要原因,因此早期诊断和干预可能有助于逆转肾脏损害。本研究于2010年4月至2012年10月在山东大学齐鲁医院招募了168例T2DM患者和56名健康志愿者(对照组)。所有受试者都接受了血清同型半胱氨酸(Hcy)和胱抑素C (Cys C)检测和尿微量白蛋白检测。根据尿微量白蛋白排泄率(UMAER)将患者分为3组:单纯DM组(SDM组,n = 51)、早期DN组(EDN组,n = 60)、临床DN合并肾功能衰竭组(CDN组,n = 57)。进行相关分析以检验血清Hcy和Cys C水平与UMAER之间的关系。结果显示,与对照组相比,SDM组、EDN组和CDN组血清Hcy水平、Cys C水平和UMAER均显著升高(P < 0.05, P < 0.01), EDN组显著升高(P < 0.01)。随着DN的进展,这3项生化指标均显著升高(P < 0.01)。相关分析显示,血清Hcy、Cys C水平与UMAER呈正相关(r = 0.702, P < 0.01;r = 0.873, P < 0.01)。总之,我们的研究结果显示,血清Hcy和Cys C水平随着DN的发生和进展而升高,正如UMAER所显示的那样。血清Hcy和Cys C是检测早期DN和监测其进展的敏感生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic value of the combined measurement of serum hcy, serum cys C, and urinary microalbumin in type 2 diabetes mellitus with early complicating diabetic nephropathy.

Diabetic nephropathy (DN) is a major cause of end-stage kidney disease, and therefore early diagnosis and intervention may help reverse renal damage. One hundred and sixty-eight patients with T2DM and 56 healthy volunteers (control group) were enrolled at Shandong University Qilu Hospital between April 2010 and October 2012. All subjects underwent blood sampling for sera homocysteine (Hcy) and cystatin C (Cys C) assays and a urine microalbumin test. The patients were divided into three groups according to the urine microalbumin excretion rate (UMAER): the simple DM group (SDM group, n = 51), the early-stage DN group (EDN group, n = 60), and the clinical DN and renal failure group (CDN group, n = 57). Correlation analysis was performed to examine the association between sera Hcy and Cys C levels with UMAER. Our findings showed that sera Hcy level, Cys C level, and UMAER increased significantly in the SDM group (P < 0.05, P < 0.01), the EDN group (P < 0.01), and the CDN group (P < 0.01) as compared with the control group. These three biochemical markers also increased significantly with DN progression (P < 0.01). Correlation analysis showed that sera Hcy and Cys C levels were positively correlated with UMAER (r = 0.702, P < 0.01; r = 0.873, P < 0.01). In conclusion, our results showed that sera Hcy and Cys C levels increased consistently with the development and progression of DN as indicated by UMAER. Sera Hcy and Cys C are sensitive biomarkers for the detection of early-stage DN and monitoring its progression.

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