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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.
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.
Abstract:
Acute chest syndrome (ACS) is a severe and potentially life-threatening complication of sickle cell disease (SCD). Early identification of patients at risk for ACS is crucial for timely intervention. There is a potential association between ACS and elevated levels of secretory phospholipase A2 (sPLA2), an enzyme involved in the breakdown of phospholipids. sPLA2 has emerged as a promising biomarker for predicting ACS. This systematic review and meta-analysis aimed to assess the diagnostic value of PLA2 in predicting ACS among children with SCD. A comprehensive search was conducted across multiple databases, including MEDLINE, Embase, Cochrane Library, PubMed, and Web of Science. Studies assessing the relationship between sPLA2 levels and ACS in SCD patients were included. Pooled sensitivity, specificity, likelihood ratios, and the area under the receiver operating characteristic curve (AUC) were calculated to assess sPLA2's diagnostic accuracy. There is a potential association between significant association between elevated sPLA2 levels and increased ACS risk in SCD patients. The pooled sensitivity of sPLA2 for predicting ACS was 0.766 (95% CI: 0.620-0.877), with a pooled specificity of 0.736 (95% CI: 0.680-0.787). The AUC of the summary receiver operating characteristic (SROC) curve was 0.84, indicating good discriminatory ability. sPLA2 emerges as a promising biomarker for predicting ACS in SCD patients, potentially guiding risk stratification and early intervention strategies to enhance patient outcomes. Nonetheless, further prospective studies are warranted to validate its clinical utility and standardize sPLA2 assay protocols.
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