DOI: 10.1002/1545-5017.70615 ISSN: 1545-5009

Secretory Phospholipase A 2 in Patients With Sickle Cell Disease Hospitalized for Vaso‐Occlusive Pain Episodes

Rawan Korman, Maria Yasmine, Dunia Hatabah, Noor Alzraikat, Frank Harris, Lou Ann Brown, Satheesh Chonat, Nitya Bakshi, Chris A. Rees, Carlton Dampier, Claudia R. Morris

ABSTRACT

Background

Secretory phospholipase A 2 (sPLA 2 ) is an inflammatory mediator linked to acute chest syndrome (ACS) in sickle cell disease (SCD), a serious complication that can develop during an acute vaso‐occlusive pain episode (VOE). Plasma sPLA 2 levels have been proposed as a potential biomarker for predicting ACS onset.

Objective

To assess serial plasma sPLA 2 levels in 105 pediatric patients hospitalized for SCD‐VOE and determine the effects of arginine therapy compared to placebo.

Procedures

This is a pharmacokinetics/pharmacodynamics and randomized controlled trial of intravenous arginine therapy. Statistical methods included t ‐tests, chi‐square, and correlation analyses.

Results

Mean age was 12.7 ± 3.7 years, 48% were male, 67% had Hb‐SS, and 70% were prescribed hydroxyurea. Using a previously established SCD‐specific cutoff of 48 ng/mL, presenting sPLA 2 levels were elevated in 33% of patients (mean sPLA 2 level 85.7 ± 32.9 ng/mL). SPLA 2 elevation in the emergency department was more common in patients with ACS compared to those without ACS (64% vs. 30%; p = 0.02; negative predictive value of 94%). Peak sPLA 2 levels were significantly higher in febrile ( n = 34) versus afebrile patients ( n = 71;101.0 ± 45.3 vs. 48.7 ± 35.4 ng/mL; p < 0.0001). Among subjects with elevated baseline sPLA 2 , arginine therapy resulted in a significant reduction in sPLA 2 levels by discharge compared to placebo (−27.8 ± 38.1 ng/mL; p = 0.002; n = 23 vs. −15.0 ± 41.2 ng/mL; p = 0.23; n = 12).

Conclusions

SPLA 2 is an underutilized biomarker of ACS given accumulating evidence of its role. In particular, low levels may identify patients at low risk for ACS. Arginine therapy may modulate inflammation in patients with SCD during VOE and/or ACS.

Trial Registration

ClinicalTrials.gov identifiers: NCT02447874; NCT02536170

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