Lupus & antiphospholipid syndrome

Positivity of antiphosphatidylserine/prothrombin antibodies identifies a subgroup of more severe antiphospholipid syndrome patients

Clin Exp RheumatolPublished Prospective descriptive study

Authors' conclusion

The increased thrombotic risk associated with the aPS/PT antibodies would justify their testing in all APS patients in complementarity with the conventional anti-phospholipid antibodies to propose the best-adjusted treatment.

Study context

Population
Patients with thrombosis (64 with known antiphospholipid syndrome (APS) per Sydney criteria) or aPL positivity (mainly lupus anticoagulant (LA)) without clinical APS, tested for anti-PS/PT, March 2019–May 2020; active neoplasia excluded128 with thrombosis
Participants
148 patients
Exposure
Anti-PS/PT positive vs negative patients
Outcome
Characterisation of anti-PS/PT and/or anti-PT-antibody-positive patients in terms of APS severity and organ damage
Methodological detailsmonocentric
  • Monocentric

Main finding

As reported in the abstract

Clinical features, anti-PS/PT positive vs negative
  • No particular thrombotic phenotype in anti-PS/PT positive patients
  • Anti-PS/PT positive vs Anti-PS/PT negative: P = 0.01
  • Anti-PS/PT positive vs Anti-PS/PT negative: P = 0.04
  • Anti-PS/PT positive vs Anti-PS/PT negative: P = 0.03
  • Anti-PS/PT positive vs Anti-PS/PT negative: P = 0.001
  • Notably in the associated-APS patient group

Observational data: associations, not effects.

Further findings

Tetra-positivity (LA+, anti-cardiolipin (aCL)+, a2βGPI+, anti-PS/PT+) and APS severity

Associated with more severe APS (thrombotic recurrences, thrombosis under anticoagulant treatment, trend of more frequent catastrophic APS)

Anti-PT antibody positivity

Agreement with anti-PS/PT antibodies
58.7%
Similar phenotype to a lesser extent

Original publication

Positivity of antiphosphatidylserine/prothrombin antibodies identifies a subgroup of more severe antiphospholipid syndrome patients. Clin Exp Rheumatol. Published 22 February 2024. doi:10.55563/clinexprheumatol/gna7r1

Composed by AI from the published abstract and checked against it. How Briefs are made →

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