Prevalence, outcome and management of patients with SLE and secondary antiphospholipid antibody syndrome after aPL seroconversion.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
02 03 2021
Historique:
received: 24 04 2020
revised: 21 06 2020
pubmed: 18 9 2020
medline: 30 6 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

The withdrawal of oral anticoagulation (OAC) in patients with SLE and secondary aPL syndrome (SAPS) who become seronegative has not been clearly investigated to date. Our aim was to evaluate the prevalence of aPL seroconversion and the prognosis of SLE patients with SAPS who withdrew OAC after aPL negativization. We retrospectively analysed data of all SLE patients (ACR criteria) with SAPS (Sydney criteria) prospectively followed-up in our clinic. aPL seroconversion was defined as negativization of lupus anticoagulant, aCL, and anti-β2glycoprotein-1 antibodies on two or more consecutive measurements, at least 12 weeks apart. OAC discontinuation was defined as the definitive withdrawal of all anticoagulants. Fifty-five out of 513 (10.7%) SLE patients had vascular SAPS. Sixteen patients (29.1%) became aPL seronegative during follow-up. Immunosuppressive therapy predicted aPL negativization (odds ratio 5.211, 95%CI 1.341, 20.243), whereas APS diagnosis prior to that of SLE (odds ratio 0.078, 95%CI 0.008, 0.799) and triple-positive profile (odds ratio 0.264, 95%CI 0.115, 0.609) were negative predictors of aPL negativization. OAC was discontinued in 13/55 patients (23.6%), after a median follow-up of 45 months (range 1-276) from aPL seroconversion. SLE-related modifiable risk factors for thrombosis were observed in 10/13 patients (77%) at the time of the thrombotic event. No thrombotic recurrences were observed during a mean follow-up time of 44 (19) months from OAC discontinuation. Our results suggest that OAC can be safely discontinued in SLE patients who became persistently seronegative for aPL, at least when aPL-related thrombotic events occurred in presence of other thrombotic risk factors.

Identifiants

pubmed: 32940703
pii: 5907564
doi: 10.1093/rheumatology/keaa463
doi:

Substances chimiques

Antibodies, Antiphospholipid 0
Anticoagulants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1313-1320

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Margherita Zen (M)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Marta Loredo Martinez (M)

Division of Rheumatology, Lozano Blesa University Clinical Hospital, Zaragoza, Spain.

Francesco Benvenuti (F)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Mariele Gatto (M)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Francesca Saccon (F)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Maddalena Larosa (M)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Luca Iaccarino (L)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

Andrea Doria (A)

Division of Rheumatology, Department of Medicine DIMED, University of Padua, Padova, Italy.

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Classifications MeSH