Küme Tuncay, Sağlam Barıs, Ergon Cem, Sisman Ali Rıza
Medical Biochemistry Department, Dokuz Eylül University Medical Faculty, Izmir, Turkey.
Central Laboratory, Dokuz Eylül University Hospital, Izmir, Turkey.
J Clin Lab Anal. 2018 Jan;32(1). doi: 10.1002/jcla.22168. Epub 2017 Feb 15.
The aim of this study is to evaluate and compare the analytical performance characteristics of the two creatinine methods based on the Jaffe and enzymatic methods.
Two original creatinine methods, Jaffe and enzymatic, were evaluated on Architect c16000 automated analyzer via limit of detection (LOD) and limit of quantitation (LOQ), linearity, intra-assay and inter-assay precision, and comparability in serum and urine samples. The method comparison and bias estimation using patient samples according to CLSI guideline were performed on 230 serum and 141 urine samples by analyzing on the same auto-analyzer.
The LODs were determined as 0.1 mg/dL for both serum methods and as 0.25 and 0.07 mg/dL for the Jaffe and the enzymatic urine method respectively. The LOQs were similar with 0.05 mg/dL value for both serum methods, and enzymatic urine method had a lower LOQ than Jaffe urine method, values at 0.5 and 2 mg/dL respectively. Both methods were linear up to 65 mg/dL for serum and 260 mg/dL for urine. The intra-assay and inter-assay precision data were under desirable levels in both methods. The higher correlations were determined between two methods in serum and urine (r=.9994, r=.9998 respectively). On the other hand, Jaffe method gave the higher creatinine results than enzymatic method, especially at the low concentrations in both serum and urine.
Both Jaffe and enzymatic methods were found to meet the analytical performance requirements in routine use. However, enzymatic method was found to have better performance in low creatinine levels.
本研究的目的是评估和比较基于杰氏法和酶法的两种肌酐检测方法的分析性能特征。
通过检测限(LOD)和定量限(LOQ)、线性、批内和批间精密度以及血清和尿液样本的可比性,在Architect c16000自动分析仪上对两种原始肌酐检测方法(杰氏法和酶法)进行评估。根据CLSI指南,使用患者样本,通过在同一自动分析仪上进行分析,对230份血清样本和141份尿液样本进行方法比较和偏差估计。
两种血清方法的检测限均确定为0.1mg/dL,杰氏法尿液检测方法的检测限为0.25mg/dL,酶法尿液检测方法的检测限为0.07mg/dL。两种血清方法的定量限相似,均为0.05mg/dL,酶法尿液检测方法的定量限低于杰氏法尿液检测方法,分别为0.5mg/dL和2mg/dL。两种方法在血清浓度高达65mg/dL和尿液浓度高达260mg/dL时均呈线性。两种方法的批内和批间精密度数据均在理想水平以下。两种方法在血清和尿液中的相关性较高(分别为r = 0.9994和r = 0.9998)。另一方面,杰氏法得出的肌酐结果高于酶法,尤其是在血清和尿液的低浓度时。
杰氏法和酶法在常规使用中均满足分析性能要求。然而,发现酶法在低肌酐水平下具有更好的性能。