2023 ACR/EULAR antiphospholipid syndrome classification criteria.
antibodies, antiphospholipid
antiphospholipid syndrome
thrombosis
Journal
Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355
Informations de publication
Date de publication:
10 2023
10 2023
Historique:
received:
21
06
2023
accepted:
21
06
2023
medline:
21
9
2023
pubmed:
29
8
2023
entrez:
28
8
2023
Statut:
ppublish
Résumé
To develop new antiphospholipid syndrome (APS) classification criteria with high specificity for use in observational studies and trials, jointly supported by the American College of Rheumatology (ACR) and EULAR. This international multidisciplinary initiative included four phases: (1) Phase I, criteria generation by surveys and literature review; (2) Phase II, criteria reduction by modified Delphi and nominal group technique exercises; (3) Phase III, criteria definition, further reduction with the guidance of real-world patient scenarios, and weighting via consensus-based multicriteria decision analysis, and threshold identification; and (4) Phase IV, validation using independent adjudicators' consensus as the gold standard. The 2023 ACR/EULAR APS classification criteria include an entry criterion of at least one positive antiphospholipid antibody (aPL) test within 3 years of identification of an aPL-associated clinical criterion, followed by additive weighted criteria (score range 1-7 points each) clustered into six clinical domains (macrovascular venous thromboembolism, macrovascular arterial thrombosis, microvascular, obstetric, cardiac valve, and hematologic) and two laboratory domains (lupus anticoagulant functional coagulation assays, and solid-phase enzyme-linked immunosorbent assays for IgG/IgM anticardiolipin and/or IgG/IgM anti-β These new ACR/EULAR APS classification criteria were developed using rigorous methodology with multidisciplinary international input. Hierarchically clustered, weighted, and risk-stratified criteria reflect the current thinking about APS, providing high specificity and a strong foundation for future APS research.
Identifiants
pubmed: 37640450
pii: ard-2023-224609
doi: 10.1136/ard-2023-224609
doi:
Substances chimiques
Autoantibodies
0
Immunoglobulin G
0
Immunoglobulin M
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1258-1270Investigateurs
Nancy Agmon-Levin
(N)
Cassyanne Aguilar
(C)
Paula Alba
(P)
Oral Alpan
(O)
Ales Ambrozic
(A)
Luis Andrade
(L)
Simone Appenzeller
(S)
Yackov Berkun
(Y)
Antonio Cabral
(A)
Guillame Canaud
(G)
Pojen Chen
(P)
Cecilia Chighizola
(C)
Rolando Cimaz
(R)
Maria Jose Cuadrado
(MJ)
Philip G de Groot
(PG)
Philippe de Moerloose
(P)
Ronald Derksen
(R)
Thomas Dörner
(T)
Paul Fortin
(P)
Bill Giannakopoulos
(B)
Emilio B Gonzalez
(EB)
Murat Inanc
(M)
Gili Kenet
(G)
Munther Khamashta
(M)
Martin Kriegel
(M)
Steven Krilis
(S)
Danyal Ladha
(D)
Patti Massicotte
(P)
Gale McCarty
(G)
Jamal Mikdashi
(J)
Barry Myones
(B)
Lisa Sammaritano
(L)
Flavio Signorelli
(F)
Arzu Soybilgic
(A)
Scott Woller
(S)
Ray Zuo
(R)
Informations de copyright
© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: RAL is an employee of GlaxoSmithKline.