Pottel Hans, Dubourg Laurence, Schaeffner Elke, Eriksen Bjørn Odvar, Melsom Toralf, Lamb Edmund J, Rule Andrew D, Turner Stephen T, Glassock Richard J, De Souza Vandréa, Selistre Luciano, Goffin Karolien, Pauwels Steven, Mariat Christophe, Flamant Martin, Bevc Sebastjan, Delanaye Pierre, Ebert Natalie
Department of Public Health and Primary Care, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
Exploration Fonctionnelle Rénale, Groupement Hospitalier Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Clin Chim Acta. 2017 Aug;471:164-170. doi: 10.1016/j.cca.2017.06.005. Epub 2017 Jun 7.
Serum creatinine (Scr) is the major contributing variable in glomerular filtration rate (GFR) estimating equations. Serum cystatin C (ScysC) based GFR estimating (eGFR)-equations have also been developed. The present study investigates the relation between 'rescaled' levels of these renal biomarkers (with reference interval of [0.67-1.33]) and measured GFR (mGFR).
We evaluated the diagnostic ability to detect impaired kidney function of the rescaled renal biomarkers in 8584 subjects from 12 cohorts with measured GFR, standardized Scr and ScysC. We calculated sensitivity and specificity of the rescaled biomarkers to identify kidney disease, with reference to a fixed (60mL/min/1.73m) as well as an age-dependent threshold for mGFR.
The upper reference limit of 1.33 for rescaled renal biomarkers is closely related to the age-dependent threshold for defining kidney status by mGFR with sensitivity and specificity for the rescaled biomarkers close to 90% for all ages. If the fixed threshold of 60mL/min/1.73m for mGFR is used, then lower specificity in children and sensitivity in older adults are observed.
Impaired kidney function can be diagnosed by rescaled renal biomarkers instead of eGFR-equations using the fixed threshold of 1.33 for all ages, consistent with an age-dependent threshold of mGFR.
血清肌酐(Scr)是肾小球滤过率(GFR)估算方程中的主要影响变量。基于血清胱抑素C(ScysC)的GFR估算(eGFR)方程也已被开发出来。本研究调查了这些肾脏生物标志物的“重新标度”水平(参考区间为[0.67 - 1.33])与实测GFR(mGFR)之间的关系。
我们评估了在12个队列的8584名受试者中,重新标度后的肾脏生物标志物检测肾功能受损的诊断能力,这些受试者均有实测GFR、标准化的Scr和ScysC。我们计算了重新标度后的生物标志物识别肾脏疾病的敏感性和特异性,参考固定的(60mL/min/1.73m²)以及mGFR的年龄依赖性阈值。
重新标度后的肾脏生物标志物的1.33的参考上限与通过mGFR定义肾脏状态的年龄依赖性阈值密切相关,重新标度后的生物标志物在所有年龄段的敏感性和特异性接近90%。如果使用mGFR的固定阈值60mL/min/1.73m²,那么在儿童中特异性较低,在老年人中敏感性较低。
通过重新标度后的肾脏生物标志物而非使用固定阈值1.33的eGFR方程,可以诊断肾功能受损,这与mGFR的年龄依赖性阈值一致。