Antiphospholipid antibody positivity and the thrombotic risk in Japanese patients with anti-neutrophil cytoplasmic antibody-associated vasculitis

Author:

Suzuki Junya1,Furuta Shunsuke1,Sugiyama Takahiro1,Iwamoto Taro1,Ikeda Kei1ORCID,Suzuki Kotaro1,Nakajima Hiroshi1

Affiliation:

1. Department of Allergy and Clinical Immunology, Chiba University , Chiba, Japan

Abstract

ABSTRACT Objectives It has been reported that 21.0–51.7% of anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) patients were antiphospholipid antibody (aPL)-positive. However, the clinical significance of aPL positivity in AAV is not fully understood. Methods We retrospectively assessed patients with AAV diagnosed from 2013 to 2020 at our hospital. Positivity of aPL was defined as positivity of anti-cardiolipin antibody, anti-cardiolipin β2 glycoprotein 1 complex antibody, and/or lupus anticoagulant at least one time during the follow-up periods. The thrombotic risk of aPL positivity was examined by multivariate analyses with the Cox regression model. Results A total of 93 patients with a median age of 71.9 years were included in the study. The median follow-up period was 35.4 months. Thirty-one patients (33.3%) were aPL-positive. Twenty-two thrombotic events occurred in 17 patients (18.3%). Thrombotic events occurred more frequently in aPL-positive patients than in aPL-negative patients (P = 0.011). Multivariate analyses with two different models identified aPL positivity as a thrombotic risk factor (hazard ratios 4.302 and 5.956, 95% confidence intervals 1.546–11.968 and 1.940–18.281, respectively). Conclusions The proportion of aPL-positive patients was 33.3%, and aPL positivity increased the thrombotic risk in Japanese patients with AAV.

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

Reference22 articles.

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3. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS);Miyakis;J Thromb Haemost,2006

4. Diagnosis and management of the antiphospholipid syndrome;David;N Engl J Med,2018

5. Antiphospholipid syndrome;Ruiz-Irastorza;Lancet,2010

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