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在慢性肾脏病的分类中,估算肾小球滤过率(eGFR)方程是否比可溯源至同位素稀释质谱法(IDMS)的血清肌酐更好?

Are eGFR equations better than IDMS-traceable serum creatinine in classifying chronic kidney disease?

作者信息

Pottel Hans, Martens Frank

机构信息

Interdisciplinary Research Center, Katholieke Universiteit Leuven Campus Kortrijk, Kortrijk, Belgium.

出版信息

Scand J Clin Lab Invest. 2009;69(5):550-61. doi: 10.1080/00365510902811253.

Abstract

OBJECTIVE

In 2002, a uniform definition of chronic kidney disease (CKD) became widely accepted. The level of glomerular filtration rate (GFR) is the pivot for staging the disease. Because GFR is not readily measured in routine clinical practice, statistical models such as the Modification of Diet in Renal Disease (MDRD) equation have been proposed for estimating GFR. The MDRD equation is gaining worldwide acceptance in assisting the diagnosis and staging of CKD.

MATERIAL AND METHODS

We use theoretical and experimental considerations based on serum creatinine (Scr) measurements obtained with an enzymatic IDMS-traceable assay and compare CKD classifications based on Scr alone with classifications based on the eGFR-MDRD and eGFR-Mayo Clinic equations.

RESULTS

Based on recently published reference intervals for enzymatically determined Scr, we show that eGFR-MDRD<60 mL/min/1.73 m(2) corresponds extremely well with Scr>upper reference limit. The different CKD stages III, IV and V can be redefined using Scr alone, resulting in 97.5% agreement.

CONCLUSION

We show that neither the MDRD study equation nor the Mayo Clinic equation add extra value to the information already contained in Scr itself. Because of the limited applicability of the eGFR equations, Scr has even more potential to assist in the diagnosis and classification of CKD than eGFR-MDRD.

摘要

目的

2002年,慢性肾脏病(CKD)的统一定义被广泛接受。肾小球滤过率(GFR)水平是该疾病分期的关键。由于在常规临床实践中GFR不易测量,因此已提出诸如肾脏病饮食改良(MDRD)方程等统计模型来估算GFR。MDRD方程在协助CKD的诊断和分期方面正获得全球认可。

材料与方法

我们基于用酶促同位素稀释质谱法(IDMS)溯源测定的血清肌酐(Scr)测量值进行理论和实验考量,并将仅基于Scr的CKD分类与基于估算肾小球滤过率(eGFR)-MDRD方程和eGFR-梅奥诊所方程的分类进行比较。

结果

基于最近发表的酶促测定Scr的参考区间,我们表明eGFR-MDRD<60 mL/(min·1.73 m²)与Scr>参考上限高度吻合。不同的CKD III期、IV期和V期可以仅使用Scr重新定义,一致性达97.5%。

结论

我们表明,MDRD研究方程和梅奥诊所方程均未为Scr本身已包含的信息增添额外价值。由于eGFR方程的适用性有限,Scr在协助CKD的诊断和分类方面甚至比eGFR-MDRD更具潜力。

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