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不同肾小球滤过率评估方程在慢性肾脏病中的应用 被引量:1

Applications of different glomerular filtration rate evaluation equations in chronic kidney disease
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摘要 目的:探讨不同肾小球滤过率(GFR)评估方程在慢性肾脏病(CKD)各期的一致性和适用性,以及血清CysC值对预测GFR的价值。方法:选取CKD住院患者160例,检测患者血清中的肌酐和CysC水平。分别通过CKD—EPICr(2009),CKD—EPICysC(2012),CKD—EPICrCysC(2012)和简化MDRD方程计算预测GFR(eGFR)值。根据美国K/DOQI指南,以简化MDRD方程的eGFR值为标准将所有患者分为CKDⅠ期、Ⅱ期、Ⅲ期和Ⅳ-Ⅴ期等4个组,并分别比较各组中各公式所得eGFR的相关性和均值的差异。结果:CKDI期的CKD—EPICr方程与CKD-EPICysC方程、CKDⅡ期的简化MDRD与CKD—EPICysC方程所得eGFR无显著相关性(P值均〉0.05);其余任意两个方程、在任意分组所得eGFR均显著正相关(P值均〈0.05)。其中,CKD—EPICr与简化MDRD方程、CKD—EPICysC与CKD—EpIcr—CvsC方程在各组均具有较高的相关性(r=0.607—0.983,P值均〈0.001)。而在CKDI期,CKD—EPICr与CKD—EPICr-CysC方程、简化MDRD与CKD-EPICysC方程、简化MDRD与CKD-EPICr-CysC方程所得eGFR相关性均较低(r值均〈0.5,P值均〈0.05)。在CKDII期,CKD-EPICr方程与CKD-EPICysC方程所得eGFR相关性较低(F0.432,P=0.011)。分别将各组中不同评估方程所得eGFR两两进行配对样本的Wilcoxon符号秩检验,在CKDⅠ-Ⅲ期三组,各评估方程所得eGFR均存在显著差异(P值均〈0.01);其中,CKD—EPICysC方程所得eGFR最低(P值均〈0.01),CKD-EPICr-CysC方程次之(P值均〈0.01),CKD-EPICr和简化MDRD方程显著高于CKD-EPICysC和CKD-EPICr-CysC方程(P值均〈0.01)。在CKDⅣ—Ⅴ期组,CKD~EPICysC方程所得eGFR显著高于另外三个公式(P值均〈0.001),尽管该组中各方程所得eGFR中位数差值均小于5ml/(min.1.73m^2)。结论:在CKDⅠ-Ⅲ期,血清CysC值对GFR的预测有重要价值,引入血CysC值的CKD—EPICysC和CKD—EPICr—CysC方程更有利于CKD的早期诊断与筛查。在CKDⅣ—Ⅴ期,不同评估方程所得eGFR具有较高一致性。 Objective: We aim to investigate the applications of different glomerular filtration rate (GFR) evaluation equations in chronic kidney disease (CKD) and the value of serum Cystatin C (Cys C) for evaluating GFR. Methods: One hundred and sixty in-patients enrolled in this study were detected for serum creafinine and Cys C. CKD-EPI Cr equation (2009) , CKD-EPI Cys C equation (2012) , CKD-EPI Cr-Cys C equation (2012) and simplified MDtLD equation were used for evaluating the eGFR of all the patients. According to American K/DOQI guidelines, all the patients were divided to CKD stage Ⅰ , CKD stage Ⅱ, CKD stage Ⅲ and CKD stage Ⅳ- Ⅴ groups, then the eGFR values from different evaluation equations were compared respectively in each group. Results: There were significant correlations between any two equations in each group (P〈0.05) , except CKD-EPI Cr equation and CKD-EPI Cys C equation in CKD stage Ⅰ group, simplified MDRD equation and CKD-EPI Cys C equation in CKD stage Ⅱ group (P〉0.05) . Of which, there were high correlations between CKD-EPI Cr equation and simplified MDRD equation、 CKD-EPI Cys C equation and CKD-EPI Cr-Cys C equation in each group (r-=0.607-0.983, P〈0.001) . In comparison, in CKD stage Ⅰ group, the correlations between CKD-EPI Cr equation and CKD-EPI Cr-Cys C equation, simplified MDRD equation and CKD-EPI Cys C equation, simplified MDRD equation and CKD-EPI Cr-Cys C equation were low (r 〈0.5, P〈0.05) . In CKD stage Ⅱ group, the correlation between CKD-EPI Cr equation and CKD-EPI Cys C equation was also low (r=0.432, P= 0.011) . Paired-sample signed rank test was used respectively to compare eGFR values from different evaluation equations in each group. In groups of CKD stage Ⅰ -Ⅲ, there was significant difference between eGFR values from different equations (P〈0.01) . There into, the eGFR values from CKD-EPI Cys C equation were the lowest (P〈0.01) , the values from CKD-EPI Cr and simplified MDRD equations were significantly higher than that from CKD-EPI Cys C and CKD-EPI Cr-Cys C equations (P〈0.01) .In CKD stageⅣ-Ⅴ group, the eGFR values from CKD-EPI Cys C equation were statistically higher than those from three other equations (P〈0.001) , despite all the median differences were less than 5 ml/(min.1.73 m^2) . Conclusion: In CKD stage Ⅰ -Ⅲ, serum Cys C is valuable for evaluating GFR, CKD-EPI Cys C and CKD-EPI Cr-Cys C equations, which introduce serum Cys C, are more conducive to early diagnosis and screening of CKD. In CKD stage Ⅳ- Ⅴ, eGFR values from different equations are of high consistency.
作者 张彩琴 林真 金福顺 滕菁 ZHANG Cai-qin LIN Zhen JIN Fushun et al(Xia Men Hospital of Traditional Chinese Medcine, FuJian Xiamen 361009)
机构地区 厦门市中医院
出处 《医学检验与临床》 2016年第8期4-8,共5页 Medical Laboratory Science and Clinics
基金 国家高技术研究发展计划(863计划)子课题.课题编号:2011AA02A111.
关键词 肾小球滤过率 评估方程 慢性肾脏病 半胱氨酸蛋白酶抑制剂C Glomerular filtration rate Evaluation equation Chronic kidney disease Cystatin C
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