Predictors and clinical complications associated with antiphospholipid antibodies in sickle cell disease

Author:

Rivera Claudia Rodriguez1,Srisuwananukorn Andrew2,Bajwa Rizma Jalees1,Gordeuk Victor R.3,Rauch Joyce4,Levine Jerrold S.15,Saraf Santosh L.3

Affiliation:

1. Department of Medicine Division of Nephrology University of Illinois at Chicago Chicago Illinois USA

2. Department of Medicine Division of Hematology and Oncology Mt Sinai Health System New York City New York USA

3. Department of Medicine Division of Hematology and Oncology University of Illinois at Chicago Chicago Illinois USA

4. Department of Medicine Division of Rheumatology Research Institute of the McGill University Health Centre McGill University Montreal Quebec Canada

5. Department of Medicine Division of Nephrology Jesse Brown, Veterans Affairs Medical Center Chicago Illinois USA

Abstract

AbstractAlthough a higher prevalence of antiphospholipid autoantibodies (aPL) has been observed in some cohorts of sickle cell disease (SCD) patients, the clinical risk factors for the development of aPL and its associated complications remain unclear. In a retrospective study of 63 SCD patients, a lower hemoglobin concentration and higher white blood cell count were independently associated with an elevated aPL. SCD patients with elevated aPL had increased pregnancy complications (≥3 miscarriages, preterm delivery, pre‐eclampsia) and venous thrombotic events. Our findings suggest that SCD may predispose to the generation of aPL and that aPL itself may contribute to the vasculopathy of SCD. Prospective testing for aPL is warranted in patients with SCD.

Funder

National Institutes of Health

Publisher

Wiley

Subject

General Earth and Planetary Sciences

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