AI Article Synopsis

  • - A study explored the potential of soluble urokinase-type plasminogen activator receptor (suPAR) as a biomarker for diagnosing acute coronary syndrome (ACS), highlighting the need for better diagnostic tools in clinical practice.
  • - The researchers conducted a meta-analysis of five studies with 3,417 participants, comparing suPAR levels in patients with ACS to those without, finding significantly higher levels in the ACS group.
  • - The findings suggest that measuring suPAR levels could improve early identification of ACS in emergency room settings, indicating its relevance as a clinical tool.

Article Abstract

Background: In contemporary clinical practice, there is an increasing need for new clinically relevant biomarkers potentially optimizing management strategies in patients with suspected acute coronary syndrome (ACS). This study aimed to determine the diagnostic utility of soluble urokinase-type plasminogen activator receptor (suPAR) levels in individuals with suspected ACS.

Methods: A literature search was performed in Web of Science, PubMed, Scopus, and the Cochrane Central Register of Controlled Trials databases, for studies comparing suPAR levels among patients with and without ACS groups. The methodological quality of the included papers was assessed using the Newcastle-Ottawa Scale (NOS). A fixed-effects model was used if I² < 50%; otherwise, the random-effects model was performed.

Results: Five studies with 3417 participants were included in the meta-analysis. Pooled analysis showed that mean suPAR levels in the ACS group were statistically significantly higher than in the control group (3.56 ± 1.38 vs. 2.78 ± 0.54 ng/mL, respectively; mean difference: 1.04; 95% confidence interval: 0.64-1.44; I² = 99%; p < 0.001).

Conclusions: In the context of acute coronary syndrome, suPAR is a potential biomarker for the early identification of medical conditions in individuals who are being treated in emergency rooms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11374330PMC
http://dx.doi.org/10.5603/cj.96228DOI Listing

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