Assessment and comparison of the 2023 ACR/EULAR APS criteria with the revised Sapporo criteria

Author:

Vasi İbrahim1ORCID,Kardaş Rıza Can1ORCID,Ekici Mustafa2,Yıldırım Derya1ORCID,Kaya Burcugül1,Duran Rahime1,Karadeniz Hazan1ORCID,Güler Aslıhan Avanoğlu1,Küçük Hamit1,Göker Berna1,Bilgen Şule Apraş2,Tufan Abdurrahman1ORCID,Öztürk Mehmet Akif1,Erden Abdulsamet1ORCID

Affiliation:

1. Division of Rheumatology, Department of Internal Medicine Gazi University Faculty of Medicine Ankara Turkey

2. Division of Rheumatology, Department of Internal Medicine Hacettepe University Faculty of Medicine Ankara Turkey

Abstract

AbstractObjectiveTo analyze antiphospholipid antibody (aPL)‐positive patients using the 2023 American College of Rheumatology/The European Alliance of Associations for Rheumatology (ACR/EULAR) antiphospholipid syndrome (APS) classification criteria and compare the revised Sapporo criteria and the 2023 ACR/EULAR criteria and evaluate whether the 2023 ACR/EULAR criteria provide added value over the revised Sapporo criteria.MethodsIn this descriptive study, 94 aPL‐positive patients (with or without APS diagnosis) were identified from two hospital‐based registries (Gazi and Hacettepe University). Patients were classified into four groups to compare both criteria sets. These four groups are as follows: (1) patients classified with only the revised Sapporo criteria; (2) patients classified with only the 2023 ACR/EULAR APS criteria; (3) patients classified with both two criteria sets; and (4) patients classified with neither two criteria set.ResultsOf the 94 patients, 11 were classified with only the revised Sapporo criteria; one with only the 2023 ACR/EULAR APS criteria; 52 with both criteria sets; and 30 with neither set of criteria. For these 94 patients, the operating characteristics of the 2023 ACR/EULAR APS criteria, using the revised Sapporo criteria as the gold standard, the 2023 ACR/EULAR APS entry criteria demonstrated 100% sensitivity, and the 2023 ACR/EULAR APS classification criteria demonstrated 98% specificity and 82.5% sensitivity.ConclusionThe study emphasizes the importance of recognizing differences in clinical manifestations, such as early pregnancy loss without severe preeclampsia (PEC) and/or severe placental insufficiency (PI) and calls for a nuanced discussion on anticardiolipin (aCL) and anti‐beta 2‐glycoprotein‐I (anti‐β2GPI) immunoglobulin G (IgG) cutoff values.

Publisher

Wiley

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