The impact of antiphospholipid antibodies/antiphospholipid syndrome on systemic lupus erythematosus

Author:

Venturelli Veronica1,Abrantes Ana Mafalda23ORCID,Rahman Anisur4ORCID,Isenberg David A4ORCID

Affiliation:

1. Rheumatology Unit, Department of Medical Sciences, Università degli Studi di Ferrara, Azienda Ospedaliero-Universitaria S. Anna , Cona, Italy

2. Division of Internal Medicine II, Centro Hospitalar Universitário Lisboa Norte , Lisbon, Portugal

3. Instituto de Semiótica Clínica, Faculty of Medicine, University of Lisbon , Lisbon, Portugal

4. Centre for Rheumatology, Department of Medicine, University College London , London, UK

Abstract

Abstract aPLs are a major determinant of the increased cardiovascular risk in patients with SLE. They adversely affect clinical manifestations, damage accrual and prognosis. Apart from the antibodies included in the 2006 revised classification criteria for APS, other non-classical aPLs might help in identifying SLE patients at increased risk of thrombotic events. The best studied are IgA anti-β2-glycoprotein I, anti-domain I β2-glycoprotein I and aPS-PT. Major organ involvement includes kidney and neuropsychiatric systems. aPL/APS severely impacts pregnancy outcomes. Due to increased thrombotic risk, these patients require aggressive cardiovascular risk factor control. Primary prophylaxis is based on low-dose aspirin in high-risk patients. Warfarin is the gold-standard drug for secondary prophylaxis.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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1. Update on antiphospholipid syndrome;Rheumatology;2024-02-01

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