Abstract

Introduction: Recurrent thrombotic events are a hallmark of Antiphospholipid Syndrome (APS). However, biomarkers to identify if a patient with antiphospholipid antibodies (aPL) is at higher risk to develop an arterial or a venous event are lacking. Recently, the pathogenic role of anti-high-density lipoproteins antibodies (anti-HDL) in the occurrence of cardiovascular disease (CVD) in autoimmunity has emerged. The aim of the present study was to evaluate the presence of IgG anti-HDL antibodies in a cohort of thrombotic APS patients and to investigate their association with clinical outcomes.Methods: Serum levels of IgG anti-HDL antibodies, total IgG, and complete aPL profile were assessed in 60 APS patients and 80 healthy donors (HDs) by immunoassays.Results: Higher levels of IgG anti-HDL were found in APS patients compared to HDs (p < 0.001), even after correcting for total IgG levels (p < 0.001). No associations with treatments or traditional cardiovascular risk factors, except for smoking habit (p < 0.0001), were found. Patients who experienced at least one arterial event (n = 30) had significantly higher levels of anti-HDL antibodies when compared to patients with venous thrombosis (n = 30, p = 0.046), this difference being stronger when adjusting for total IgG (p = 0.007). Additionally, patients tested positive for antiphosphatidylserine/prothrombin (IgG/IgM) antibodies had significantly higher levels of anti-HDL antibodies (p = 0.045).Conclusions: Increased levels of IgG anti-HDL antibodies can be found in APS, mainly in patients with arterial thrombosis, independently of aPL antibodies and traditional risk factors. These findings point to a role of anti-HDL antibodies in APS and support their use as a potential biomarker for arterial thrombotic events.

Highlights

  • Recurrent thrombotic events are a hallmark of Antiphospholipid Syndrome (APS)

  • Premature cardiovascular disease (CVD) and atherosclerotic development have been proven to be more prevalent in APS compared to the general population [2, 3].The mechanisms underlying thrombosis and CVD in APS patients are not completely understood, but recent evidences have brought to light the existence of a complex interplay between conventional cardiovascular risk factors and disease-specific features, such as the presence of autoantibodies [4]

  • Sixty APS patients were enrolled in this study, 43 (71.6%) patients being primary APS patients (PAPS) and 17 (28.4%) patients having a concomitant diagnosis of SLE, according to the recently approved classification criteria of the European League Against Rheumatism and the American College of Rheumatology, which includes at least one positive antinuclear antibody test and the combination of a number of clinical and immunological criteria [14]

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Summary

Introduction

Biomarkers to identify if a patient with antiphospholipid antibodies (aPL) is at higher risk to develop an arterial or a venous event are lacking. The aim of the present study was to evaluate the presence of IgG anti-HDL antibodies in a cohort of thrombotic APS patients and to investigate their association with clinical outcomes. While it is known that the presence of aPL confers a high risk for thrombosis [11], biomarkers to if a patient is at higher risk to develop an arterial or a venous event are lacking. The aim of the present study was to evaluate the presence of IgG anti-HDL antibodies in a cohort of thrombotic APS patients and to investigate if these antibodies can discriminate between arterial and venous thrombosis

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