Lee Min Jung, Jung Chang Hee, Kang Yu Mi, Jang Jung Eun, Leem Jaechan, Park Joong-Yeol, Lee Woo Je
Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Diabetes Metab J. 2015 Jun;39(3):230-9. doi: 10.4093/dmj.2015.39.3.230. Epub 2015 Apr 22.
Oxidative stress is known to be associated with progression of diabetic kidney disease. Ceruloplasmin acts as a pro-oxidant under conditions of severe oxidative stress. Thus, we conducted a longitudinal observational study to evaluate whether the serum ceruloplasmin level is a predictive biomarker for progression of diabetic nephropathy.
A total of 643 Korean men with type 2 diabetes mellitus were enrolled. Serum ceruloplasmin was measured using a nephelometric method. Progression of diabetic nephropathy was defined as transition in albuminuria class (i.e., normoalbuminuria to microalbuminuria, microalbuminuria to macroalbuminuria, or normoalbuminuria to macroalbuminuria) and/or a greater than 2-fold increase of serum creatinine at follow-up compared with the baseline value.
During the follow-up period (median, 2.7 years; range, 0.3 to 4.4 years), 49 of 643 patients (7.6%) showed the progression of diabetic nephropathy and three patients (0.5%) developed end-stage renal disease. Baseline ceruloplasmin levels were higher in the progressors than in the nonprogressors (262.6±40.9 mg/L vs. 233.3±37.8 mg/L, P<0.001). Kaplan-Meier analysis showed a significantly higher incidence of nephropathy progression according to ceruloplasmin tertile (log-rank test, P<0.001). The hazard ratio (HR) for progression of diabetic nephropathy was significantly higher in the highest ceruloplasmin tertile category compared with the lowest ceruloplasmin tertile category, even after adjusting for confounding variables (HR, 3.32; 95% confidence interval, 1.28 to 8.61; P=0.003).
Baseline serum ceruloplasmin is an independent predictive factor for the progression of diabetic nephropathy in patients with type 2 diabetes mellitus.
已知氧化应激与糖尿病肾病的进展相关。在严重氧化应激条件下,铜蓝蛋白作为一种促氧化剂发挥作用。因此,我们开展了一项纵向观察性研究,以评估血清铜蓝蛋白水平是否为糖尿病肾病进展的预测生物标志物。
共纳入643名韩国2型糖尿病男性患者。采用散射比浊法测定血清铜蓝蛋白。糖尿病肾病的进展定义为蛋白尿类别转变(即正常蛋白尿转变为微量白蛋白尿、微量白蛋白尿转变为大量白蛋白尿或正常蛋白尿转变为大量白蛋白尿)和/或随访时血清肌酐较基线值升高超过2倍。
在随访期间(中位数为2.7年;范围为0.3至4.4年),643例患者中有49例(7.6%)出现糖尿病肾病进展,3例患者(0.5%)发展为终末期肾病。进展者的基线铜蓝蛋白水平高于未进展者(262.6±40.9mg/L对233.3±37.8mg/L,P<0.001)。Kaplan-Meier分析显示,根据铜蓝蛋白三分位数分组,肾病进展的发生率显著更高(对数秩检验,P<0.001)。即使在调整混杂变量后,与最低铜蓝蛋白三分位数组相比,最高铜蓝蛋白三分位数组糖尿病肾病进展的风险比(HR)也显著更高(HR为3.32;95%置信区间为1.28至8.61;P=0.003)。
基线血清铜蓝蛋白是2型糖尿病患者糖尿病肾病进展的独立预测因素。