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抗磷脂抗体检测缺乏标准化可能有利于在抗磷脂综合征分类中使用第99百分位数临界值。

The absence of standardization in antiphospholipid antibody testing may favor the use of 99th percentile cutoffs in antiphospholipid syndrome classification.

作者信息

Anunciación-Llunell Ariadna, Marques-Soares Joana, Ockova Monika, Pozuelo Natalia, Esteve-Valverde Enrique, Andrada Catalina, Alijotas-Reig Jaume, Miró-Mur Francesc A

机构信息

Systemic Autoimmune Diseases Research Unit, Vall d'Hebron Institut de Recerca, Barcelona, Spain.

Department of Internal Medicine, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

出版信息

Res Pract Thromb Haemost. 2025 Jul 7;9(5):102967. doi: 10.1016/j.rpth.2025.102967. eCollection 2025 Jul.

Abstract

BACKGROUND

Classification criteria for antiphospholipid syndrome (APS) issued by the American College of Rheumatology/European Alliance of Associations for Rhuematology necessitate a positivity for any of the 3 molecular targets: lupus anticoagulant, anticardiolipin (aCL) immunoglobulin G, or anti-β2 glycoprotein I (aβ2GPI) immunoglobulin G, with the latter 2 requiring concentrations > 40 units. This specification implies having standardized and comparable calibration strategies to achieve proper patient classification. In the past, calibrator tests suffered from poor standardization; thus, the 99th percentile was established as the cutoff point.

OBJECTIVES

We aimed to find a balance between sensitivity and specificity in the laboratory criteria for patient enrollment in APS studies by harmonizing the 99th percentile and 40-unit threshold.

METHODS

In a cohort of 250 healthy individuals, we tested aCL and aβ2GPI concentrations by 4 different methods: 3 colorimetric, standardized ELISA platforms and 1 chemiluminescence assay, to define the 99th percentile. We tested cross-reactivity of standardized calibrators between kits and how to implement better accuracy for patient enrollment in a cohort of 80 APS patients.

RESULTS

We found that the 99th percentile was substantially <40-unit cutoff and observed considerable interkit variability in the determined cutoffs, which originated from the inadequate standardization of kit calibrators. In a second cohort of 80 APS patients, we estimated the accuracy of these different methods by comparing the 99th percentile and 40-unit cutoffs. For certain ELISA kits, using a fixed cutoff of 40 units instead of the 99th percentile decreased their sensitivity without increasing specificity, which affected patient classification and thus the number of patients eligible for APS studies. Testing with 2 ELISA platforms at the 99th percentile cutoff would improve patient eligibility.

CONCLUSION

Our survey suggests that in the absence of standardized calibrators for testing aCL or aβ2GPI, a cutoff point at the 99th percentile of 2 different ELISA kits should be adopted.

摘要

背景

美国风湿病学会/欧洲风湿病联盟协会发布的抗磷脂综合征(APS)分类标准要求3种分子靶点中的任何一种呈阳性:狼疮抗凝物、抗心磷脂(aCL)免疫球蛋白G或抗β2糖蛋白I(aβ2GPI)免疫球蛋白G,后两者要求浓度>40单位。该规范意味着要有标准化且可比的校准策略,以实现对患者的正确分类。过去,校准物检测的标准化程度较差;因此,将第99百分位数确定为临界值。

目的

我们旨在通过协调第99百分位数和40单位阈值,在APS研究患者入组的实验室标准中找到敏感性和特异性之间的平衡。

方法

在250名健康个体组成的队列中,我们通过4种不同方法检测aCL和aβ2GPI浓度:3种比色法、标准化酶联免疫吸附测定(ELISA)平台和1种化学发光测定法,以确定第99百分位数。我们测试了试剂盒之间标准化校准物的交叉反应性,以及如何在80名APS患者的队列中为患者入组实现更高的准确性。

结果

我们发现第99百分位数远低于40单位临界值,并且在确定的临界值中观察到试剂盒间存在相当大的变异性,这源于试剂盒校准物标准化不足。在另一组80名APS患者中,我们通过比较第99百分位数和40单位临界值来估计这些不同方法的准确性。对于某些ELISA试剂盒,使用固定的40单位临界值而非第99百分位数会降低其敏感性,而不会提高特异性,这会影响患者分类,进而影响符合APS研究条件的患者数量。在第99百分位数临界值下使用2种ELISA平台进行检测将提高患者入选资格。

结论

我们的调查表明,在缺乏用于检测aCL或aβ2GPI的标准化校准物的情况下,应采用2种不同ELISA试剂盒第99百分位数的临界值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/971b/12320162/7149d5a4c93c/ga1.jpg

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