Characteristics of Patients With Antiphospholipid Antibody Positivity in the APS ACTION International Clinical Database and Repository.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
02 2022
Historique:
revised: 04 09 2020
received: 24 01 2020
accepted: 22 09 2020
pubmed: 29 9 2020
medline: 15 2 2022
entrez: 28 9 2020
Statut: ppublish

Résumé

To describe the baseline characteristics of patients with positivity for antiphospholipid antibodies (aPLs) who were enrolled in an international registry, the Antiphospholipid Syndrome (APS) Alliance for Clinical Trials and International Networking (APS ACTION) clinical database and repository, overall and by clinical and laboratory subtypes. The APS ACTION registry includes adults who persistently had positivity for aPLs. We evaluated baseline sociodemographic and aPL-related (APS classification criteria and "non-criteria") characteristics of patients overall and in subgroups (aPL-positive without APS, APS overall, thrombotic APS only, obstetric APS only, and both thrombotic APS/obstetric APS). We assessed baseline characteristics of patients tested for the presence of three aPLs (lupus anticoagulant [LAC] test, anticardiolipin antibody [aCL], and anti-β The 804 aPL-positive patients assessed in the present study had a mean age of 45 ± 13 years, were 74% female, and 68% White; additionally, 36% had other systemic autoimmune diseases. Of these 804 aPL-positive patients, 80% were classified as having APS (with 55% having thrombotic APS, 9% obstetric APS, and 15% thrombotic APS/obstetric APS). In the overall cohort, 71% had vascular thrombosis, 50% with a history of pregnancy had obstetric morbidity, and 56% had experienced at least one non-criteria manifestation. Among those with three aPLs tested (n = 660), 42% were triple aPL-positive. While single-, double-, and triple aPL-positive subgroups had similar frequencies of vascular, obstetric, and non-criteria events, these events were lowest in the single aPL subgroup, which consisted of aCLs or anti-β Our study demonstrates the heterogeneity of aPL-related clinical manifestations and laboratory profiles in a multicenter international cohort. Within single aPL positivity, LAC may be a major contributor to clinical events. Future prospective analyses, using standardized core laboratory aPL tests, will help clarify aPL risk profiles and improve risk stratification.

Identifiants

pubmed: 32986935
doi: 10.1002/acr.24468
doi:

Substances chimiques

Antibodies, Antiphospholipid 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

324-335

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR069572
Pays : United States
Organisme : Canada Research Chairs
Organisme : NIH HHS
ID : R01-AR069572
Pays : United States
Organisme : Rheumatology Research Foundation
Organisme : Clinical and Translational Science Center at Weill Cornell Medical College
ID : UL1-TR000457

Informations de copyright

© 2020, American College of Rheumatology.

Références

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Auteurs

Ecem Sevim (E)

Hospital for Special Surgery, New York, New York, and Montefiore Medical Center, Bronx, New York.

Diane Zisa (D)

Hospital for Special Surgery and Weill Cornell Medicine, New York, New York.

Danieli Andrade (D)

University of Sao Paulo, Sao Paulo, Brazil.

Savino Sciascia (S)

University of Turin, Turin, Italy.

Vittorio Pengo (V)

University Hospital Padova, Padova, Italy.

Maria G Tektonidou (MG)

National and Kapodistrian University of Athens, Athens, Greece.

Amaia Ugarte (A)

Hospital Universitario Cruces, Barakaldo, País Vasco, Spain.

Maria Gerosa (M)

University of Milan, Milan, Italy.

H Michael Belmont (HM)

New York University Langone Medical Center, New York, New York.

Maria Angeles Aguirre Zamorano (MAA)

Maimonides Institute for Biomedical Research of Cordoba, Cordoba, Spain.

Paul R Fortin (PR)

CHU de Québec and Université Laval, Quebec City, Canada.

Lanlan Ji (L)

Peking University First Hospital, Beijing, China.

Maria Efthymiou (M)

University College London, London, UK.

Hannah Cohen (H)

University College London, London, UK.

D Ware Branch (DW)

University of Utah and Intermountain Healthcare, Salt Lake City, Utah.

Guilherme Ramires de Jesus (GR)

Rio de Janeiro State University, Rio de Janeiro, Brazil.

Laura Andreoli (L)

University of Brescia, Brescia, Italy.

Michelle Petri (M)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Esther Rodriguez (E)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Ricard Cervera (R)

Hospital Clínic Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Catalonia, Spain.

Jason S Knight (JS)

University of Michigan, Ann Arbor.

Tatsuya Atsumi (T)

Hokkaido University Hospital, Sapporo, Japan.

Rohan Willis (R)

University of Texas Medical Branch, Galveston.

Robert Roubey (R)

University of North Carolina, Chapel Hill.

Maria Laura Bertolaccini (ML)

St Thomas' Hospital, London, UK.

Doruk Erkan (D)

Hospital for Special Surgery and Weill Cornell Medicine, New York, New York.

Medha Barbhaiya (M)

Hospital for Special Surgery and Weill Cornell Medicine, New York, New York.

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