This is the authors' abstract. We don't add key points for this paper.
Previous research suggests that group IIA‐secreted phospholipase A 2 (sPLA 2 ‐IIA) plays a role in and predicts lethal COVID‐19 disease. The current study reanalyzed a longitudinal proteomic data set to determine the temporal relationship between levels of several members of a family of sPLA 2 isoforms and the severity of COVID‐19 in 214 ICU patients. The levels of six secreted PLA 2 isoforms, sPLA 2 ‐IIA, sPLA 2 ‐V, sPLA 2 ‐X, sPLA 2 ‐IB, sPLA 2 ‐IIC, and sPLA 2 ‐XVI, increased over the first 7 ICU days in those who succumbed to the disease but attenuated over the same time period in survivors. In contrast, a reversed pattern in sPLA 2 ‐IID and sPLA 2 ‐XIIB levels over 7 days suggests a protective role of these two isoforms. Furthermore, decision tree models demonstrated that sPLA 2 ‐IIA outperformed top‐ranked cytokines and chemokines as a predictor of patient outcome. Taken together, proteomic analysis revealed temporal sPLA 2 patterns that reflect the critical roles of sPLA 2 isoforms in severe COVID‐19 disease.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Lu et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: