Secretory Phospholipase A2 as a Promising Biomarker for Predicting Acute Chest Syndrome in Children With Sickle Cell

Mohammed Alsabri1, Ahmed B Elsnhory2, Omar Alattar3

  • 1Paediatrics, Brookdale University Hospital Medical Center, Brooklyn, USA.

Cureus
|October 14, 2024
PubMed

Insights

Secretory phospholipase A2 (sPLA2) shows promise as a biomarker for predicting acute chest syndrome (ACS) in children with sickle cell disease (SCD). Elevated sPLA2 levels are associated with increased ACS risk, aiding early intervention.

Area of Science:

  • Hematology
  • Biomarker Discovery
  • Diagnostic Accuracy

Background:

  • Acute chest syndrome (ACS) is a critical complication of sickle cell disease (SCD).
  • Early identification of patients at risk for ACS is vital for timely intervention.
  • Secretory phospholipase A2 (sPLA2) is implicated in phospholipid metabolism and may be associated with ACS.

Purpose of the Study:

  • To systematically review and meta-analyze the diagnostic value of secretory phospholipase A2 (sPLA2) in predicting acute chest syndrome (ACS) in children with sickle cell disease (SCD).

Main Methods:

  • A comprehensive literature search was performed across major databases (MEDLINE, Embase, Cochrane Library, PubMed, Web of Science).
  • Studies investigating the relationship between sPLA2 levels and ACS in SCD patients were included.
  • Pooled diagnostic accuracy metrics, including sensitivity, specificity, and AUC, were calculated.

Main Results:

  • Elevated sPLA2 levels were significantly associated with an increased risk of ACS in SCD patients.
  • The pooled sensitivity for sPLA2 in predicting ACS was 0.766 (95% CI: 0.620-0.877).
  • The pooled specificity was 0.736 (95% CI: 0.680-0.787), with an AUC of 0.84, indicating good discriminatory ability.

Conclusions:

  • Secretory phospholipase A2 (sPLA2) demonstrates potential as a valuable biomarker for predicting ACS in pediatric SCD patients.
  • sPLA2 may aid in risk stratification and facilitate early intervention strategies to improve patient outcomes.
  • Further prospective studies are recommended to confirm clinical utility and standardize sPLA2 assay methods.

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