Laboratoire d'Immunologie, Hôpital Européen Georges Pompidou, APHP, Université de Paris Cité, Paris, France.
Laboratory of Clinical Pathology, San Antonio Hospital, Azienda Sanitaria Universitaria Integrata, Udine, Italy.
Clin Chem Lab Med. 2022 Jun 24;60(9):1373-1383. doi: 10.1515/cclm-2022-0411. Print 2022 Aug 26.
No reference data are available on repositories to measure precision of autoantibody assays. The scope of this study was to document inter- and intra-run variations of quantitative autoantibody assays based on a real-world large international data set.
Members of the European Autoimmunity Standardisation Initiative (EASI) group collected the data of intra- and inter-run variability obtained with assays quantifying 15 different autoantibodies in voluntary participating laboratories from their country. We analyzed the impact on the assay performances of the type of immunoassay, the number of measurements used to calculate the coefficient of variation (CVs), the nature and the autoantibody level of the internal quality control (IQC).
Data were obtained from 64 laboratories from 15 European countries between February and October 2021. We analyzed 686 and 1,331 values of intra- and inter-run CVs, respectively. Both CVs were significantly dependent on: the method of immunoassay, the level of IQC with higher imprecision observed when the antibody levels were lower than 2-fold the threshold for positivity, and the nature of the IQC with commercial IQCs having lower CVs than patients-derived IQCs. Our analyses also show that the type of autoantibody has low impact on the assay' performances and that 15 measurements are sufficient to establish reliable intra- and inter-run variations.
This study provides for the first time an international repository yielding values of intra- and inter-run variation for quantitative autoantibody assays. These data could be useful for ISO 15189 accreditation requirements and will allow clinical diagnostic laboratories to assure quality of patient results.
目前尚无关于检测自身抗体分析精密度的参考数据库。本研究的目的是基于真实的国际大型数据集,记录定量自身抗体分析的批内和批间差异。
欧洲自身免疫标准化倡议(EASI)小组成员收集了来自各国自愿参与实验室的 15 种不同自身抗体定量检测分析的批内和批间变异性数据。我们分析了免疫分析类型、用于计算变异系数(CV)的测量次数、内部质量控制(IQC)的性质和自身抗体水平对分析性能的影响。
2021 年 2 月至 10 月,我们从 15 个欧洲国家的 64 个实验室获得了数据。我们分析了 686 个和 1331 个批内和批间 CV 值。这两种 CV 值都显著依赖于免疫分析方法、IQC 的水平,当抗体水平低于阳性阈值的 2 倍时,会出现更高的不精密度,以及 IQC 的性质,商业 IQC 的 CV 值低于患者来源的 IQC。我们的分析还表明,自身抗体的类型对分析性能的影响较低,15 次测量足以建立可靠的批内和批间变异。
本研究首次提供了定量自身抗体分析的批内和批间变异的国际数据库。这些数据可用于 ISO 15189 认证要求,并将允许临床诊断实验室确保患者结果的质量。