Laverty Pathology, North Ryde, New South Wales, Australia.
Clin Chem. 2012 Mar;58(3):531-42. doi: 10.1373/clinchem.2011.172155. Epub 2012 Jan 9.
Vitamin D testing is increasing worldwide. Recently several diagnostic manufacturers including Abbott and Siemens have launched automated 25-hydroxy vitamin D (25OH-D) immunoassays. Furthermore, preexisting assays from DiaSorin and Roche have recently been modified. We compared the performance of 5 automated immunoassays, an RIA and 2 liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods.
Aliquots of 170 randomly selected patient samples were prepared and 25OH-D was measured by 2 LC-MS/MS methods, an RIA (DiaSorin), and automated immunoassays from Abbott (Architect), DiaSorin (LIAISON), IDS (ISYS), Roche (E170, monoclonal 25OH-D(3) assay), and Siemens (Centaur). Within-run and between-run imprecision were evaluated by measurement of 5 replicates of 2 serum pools on 5 consecutive days.
The LC-MS/MS methods agreed, with a concordance correlation coefficient (CCC) of 0.99 and bias of 0.56 μg/L (1.4 nmol/L). The RIA assay showed a performance comparable to LC-MS/MS, with a CCC of 0.97 and a mean bias of 1.1 μg/L (2.7 nmo/L). All immunoassays measured total 25OH-D (including D(3) and D(2)), with the exception of the Roche assay (D(3) only). Among the immunoassays detecting total 25OH-D, the CCCs varied between 0.85 (Abbott) to 0.95 (LIAISON). The mean bias ranged between 0.2 μg/L (0.5 nmol/L) (LIAISON) and 4.56 μg/L (11.4 nmol/L) (Abbott). The Roche 25OH-D(3) assay demonstrated small mean bias [-2.7 μg/L (-6.7 nmol/L)] [-2.7 μg/L (-6.7 nmol/L)] but a low CCC of just 0.66. Most assays demonstrated good intra- and interassay precision, with CV <10%.
Automated immunoassays demonstrated variable performance and not all tests met our minimum performance goals. It is important that laboratories be aware of the limitations of their assay.
维生素 D 检测在全球范围内不断增加。最近,包括雅培和西门子在内的几家诊断制造商推出了自动化 25-羟维生素 D(25OH-D)免疫分析。此外,DiaSorin 和罗氏的现有检测方法最近也进行了修改。我们比较了 5 种自动化免疫分析、一种 RIA 和 2 种液相色谱-串联质谱(LC-MS/MS)方法的性能。
从 170 名随机患者样本中提取样本,并用 2 种 LC-MS/MS 方法、RIA(DiaSorin)和 Abbott(Architect)、DiaSorin(LIAISON)、IDS(ISYS)、罗氏(E170,单克隆 25OH-D(3) 检测)和西门子(Centaur)的自动化免疫分析方法检测 25OH-D。通过连续 5 天测量 2 个血清池的 5 个重复样本,评估批内和批间精密度。
LC-MS/MS 方法之间具有很好的一致性,相关系数(CCC)为 0.99,偏差为 0.56μg/L(1.4nmol/L)。RIA 检测方法的性能与 LC-MS/MS 相当,CCC 为 0.97,平均偏差为 1.1μg/L(2.7nmol/L)。所有免疫分析方法均检测总 25OH-D(包括 D(3)和 D(2)),罗氏检测方法除外(仅检测 D(3))。在检测总 25OH-D 的免疫分析方法中,CCC 范围在 0.85(雅培)至 0.95(LIAISON)之间。平均偏差范围在 0.2μg/L(0.5nmol/L)(LIAISON)和 4.56μg/L(11.4nmol/L)(雅培)之间。罗氏 25OH-D(3) 检测方法显示出较小的平均偏差[-2.7μg/L(-6.7nmol/L)] [-2.7μg/L(-6.7nmol/L)],但 CCC 仅为 0.66,较低。大多数检测方法显示出良好的批内和批间精密度,CV<10%。
自动化免疫分析方法的性能存在差异,并非所有检测方法都达到了我们的最低性能要求。实验室了解其检测方法的局限性非常重要。