Secretory phospholipase A2 predicts impending acute chest syndrome in sickle cell disease

Author:

Styles Lori A.1,Aarsman Anton J.1,Vichinsky Elliott P.1,Kuypers Frans A.1

Affiliation:

1. From the Department of Hematology/Oncology, Children's Hospital Oakland, and Children's Hospital Oakland Research Institute, Oakland, CA; and the Center for Biomembranes and Lipid Enzymology, Department of Lipid Biochemistry, University of Utrecht, the Netherlands.

Abstract

Abstract Acute chest syndrome (ACS) is the leading cause of death in sickle cell disease. Severe ACS often develops in the course of a vaso-occlusive crisis (VOC), but currently there are no predictors for its development. Secretory phospholipase A2(sPLA2), a potent inflammatory mediator, is elevated in ACS, and previous work suggests that sPLA2 predicts impending ACS. We prospectively evaluated sPLA2concentration during 21 admissions for VOC; 6 of these patients went on to develop ACS. Elevation of sPLA2 was detected all 6 patients 24 to 48 hours before ACS was clinically diagnosed. Adding the requirement for fever raised the specificity of sPLA2 to 87% while retaining 100% sensitivity. These data indicate that sPLA2 can be useful in alerting the clinician to patients with impending ACS. In addition, sPLA2 may be useful for instituting early therapies to prevent or reduce the clinical morbidity of ACS.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference19 articles.

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