Cantera Estefanía Rodrigo, Gálvez Sánchez Rafael, Abando Casuso María, Flores García José Antonio, García Ruiz Raquel, Gorostidi Álvarez Irene, Cruz Barquín Héctor, Oviedo Madrid María, Herrero López Marina, Gabrie Rodríguez Ligia Gabriela, Domínguez García Juan José, García Ascacíbar Ariadna, Hernández Hernández José Luis, Yáñez San Segundo Lucrecia, González-Mesones Galán Belén, González Ponte María Luisa, López Hoyos Marcos, Méndez Navarro Gala Aglaia, Del Barrio Longarela Sara, Martínez Taboada Víctor Manuel
Division of Hematology, Hospital Universitario de Navarra, Pamplona, Spain.
Division of Rheumatology, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain.
Clin Chem Lab Med. 2025 Jul 14. doi: 10.1515/cclm-2025-0508.
The 2023 ACR/EULAR criteria aim to improve the classification of antiphospholipid syndrome (APS). This study aims to validate these criteria and compare clinical and laboratory domains between classified and non-classified patients.
A retrospective cohort study was conducted at the Hospital Universitario Marqués de Valdecilla, a tertiary referral center in Cantabria, Spain. Data were retrieved from the laboratory information system, identifying patients with at least one positive determination of lupus anticoagulant (LA), anticardiolipin (aCL), or anti-β2 glycoprotein I (anti-β2GPI) between January 2018 and March 2024. Patients were classified according to the 2006 Sydney and 2023 ACR/EULAR criteria.
Among 375 patients meeting the Sydney criteria, 152 (40.6 %) fulfilled the 2023 ACR/EULAR criteria. The sensitivity and specificity of the 2023 ACR/EULAR criteria were 30.2 and 97.7 % respectively, with a positive predictive value of 0.84, and a negative predictive value of 0.77. Area under the ROC curve was 0.639 (95 % CI: 0.605-0.673). The exclusion of thrombosis with high-risk thrombotic profiles and recurrent pregnancy loss or fetal death as individual events on obstetric APS accounted for most declassified patients. Additionally, patients meeting the 2023 ACR/EULAR criteria had a higher prevalence of arterial thrombosis without cardiovascular risk factors. In laboratory domains, isolated IgM aPL positivity was a major exclusion factor due to its lower weight in the new criteria.
The 2023 ACR/EULAR criteria enhance specificity but significantly reduce sensitivity, excluding many APS patients, particularly those with obstetric APS or IgM aPL. This raises concerns about clinical trial eligibility and applicability in diverse populations.
2023年美国风湿病学会(ACR)/欧洲抗风湿病联盟(EULAR)标准旨在改进抗磷脂综合征(APS)的分类。本研究旨在验证这些标准,并比较分类患者和未分类患者的临床及实验室指标。
在西班牙坎塔布里亚的三级转诊中心巴尔德西利亚侯爵大学医院进行了一项回顾性队列研究。从实验室信息系统中检索数据,确定2018年1月至2024年3月期间狼疮抗凝物(LA)、抗心磷脂(aCL)或抗β2糖蛋白I(抗β2GPI)至少一项检测呈阳性的患者。根据2006年悉尼标准和2023年ACR/EULAR标准对患者进行分类。
在符合悉尼标准的375例患者中,152例(40.6%)符合2023年ACR/EULAR标准。2023年ACR/EULAR标准的敏感性和特异性分别为30.2%和97.7%,阳性预测值为0.84,阴性预测值为0.77。ROC曲线下面积为0.639(95%CI:0.605 - 0.673)。排除具有高风险血栓形成特征的血栓形成以及产科APS中复发性流产或胎儿死亡作为个体事件是导致大多数患者未被分类的原因。此外,符合2023年ACR/EULAR标准的患者无心血管危险因素的动脉血栓形成患病率更高。在实验室指标方面,孤立的IgM型抗磷脂抗体(aPL)阳性是一个主要排除因素,因为其在新标准中的权重较低。
2023年ACR/EULAR标准提高了特异性,但显著降低了敏感性,排除了许多APS患者,尤其是产科APS或IgM型aPL患者。这引发了对临床试验入选资格以及在不同人群中适用性的担忧。