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Plasma glycooxidation protein products in type 2 diabetic patients with nephropathy

微量白蛋白尿 糖尿病肾病 肌酐 蛋白尿 内科学 内分泌学 肾病 糖基化 医学 糖尿病 肾功能 白蛋白 泌尿科 2型糖尿病 化学
作者
Agnieszka Piwowar,Maria Knapik-Kordecka,Joanna Szczecińska,Maria Warwas
出处
期刊:Diabetes-metabolism Research and Reviews [Wiley]
卷期号:24 (7): 549-553 被引量:34
标识
DOI:10.1002/dmrr.885
摘要

Abstract Background In diabetes mellitus, hyperglycaemia accelerates non‐enzymatic glycation and oxidative stress leading to damage of macromolecules, among others proteins. This manifests in the increased levels of advanced glycation end products (AGE) and advanced oxidation protein products (AOPP). Objectives To assess the plasma levels of AGE and AOPP in the patients with type 2 diabetes mellitus (T2DM) and to estimate its relation and connection with the degree of nephropathy. Material and Methods In 121 diabetic patients and 22 healthy people plasma levels of AGE and AOPP were determined with fluorimetric and spectrophotometric methods, respectively. To estimate nephropathy stage, albumin/creatinine ratio was calculated on the basis of albumin and creatinine concentrations in early morning urine samples. Results Diabetic patients had significantly higher levels of AGE and AOPP in comparison to healthy people. Both parameters were increasing progressively from normoalbuminuria, through microalbuminuria to macroalbuminuria. Statistically, the most significant differences were observed in AOPP concentration between separated groups. AGE fluorescence was significantly different on the same low, statistical level between patients with normoalbuminuria when compared to those with micro‐ and macroalbuminuria. Plasma AGE correlated significantly with urinary albumin/creatinine ratio whereas AOPP correlated with plasma creatinine level. Conclusions The connection between plasma levels of both glycooxidation protein products—AGE and AOPP with nephropathy severity, measured by the degree of albuminuria, in T2DM patients was observed. We can suggest that the AOPP better reflect the progression of kidney damage than AGE in examined diabetic patients. Copyright © 2008 John Wiley & Sons, Ltd.
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