Key result
Elevated pentraxin-3 linked to ~2.1-fold higher mortality risk in patients with CAD.
Why the study?
The association between plasma pentraxin-3 levels and clinical outcomes in patients with coronary artery disease remains not fully determined.
Meta-Analysis (n=11,007)
Relative Risk: 2.09 (95% CI 1.6–2.74)
p-value: p=<0.001
Background: Association between plasma pentraxin-3 (PTX-3) and clinical outcomes in patients with coronary artery disease (CAD) remains not fully determined. An updated meta-analysis of cohort studies was performed to systematically evaluate the association. Methods: Cohort studies evaluating the association between plasma PTX-3 and adverse outcomes [mortality and major adverse cardiovascular events (MACEs)] in adults with CAD were identified by systematic search of PubMed, Embase, and Web of Science databases. Only studies with multivariate analysis were included. A random-effects model incorporating the potential intrastudy heterogeneity was used for the meta-analysis. Results: A total of 16 studies including 11,007 patients were included. Pooled results showed that patients with highest level of PTX-3 were independently associated with higher risk of mortality [adjusted risk ratio (RR): 2.09, 95% CI: 1.60 to 2.74, p < 0.001; I2 = 50%] and MACEs (adjusted RR: 1.80, 95% CI: 1.43 to 2.28, p < 0.001; I2 = 49%). Subgroup analyses showed that the associations between PTX-3 and poor prognosis in CAD were consistent in patients with ST-segment elevation myocardial infraction, non-ST-segment elevation acute coronary syndrome, and stable CAD (p < 0.05 for each subgroup). Besides, the association between PTX-3 and increased incidence of mortality and MACEs were consistent in short-term (within 1 year) and long-term (over 1 year) studies and in studies with or without adjustment of C-reactive protein (CRP) (p < 0.05 for each subgroup). Conclusion: Higher plasma PTX-3 is associated with poor prognosis in patients with CAD, which may be independent of the CAD subtype, follow-up durations, and adjustment of CRP.
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Ding et al. (2022) conducted a meta-analysis in Coronary Artery Disease (CAD) (n=11,007). Highest level of plasma pentraxin-3 (PTX-3) vs. Lowest level of plasma PTX-3 was evaluated on Mortality (RR 2.09, 95% CI 1.60 to 2.74, p=<0.001). The highest level of plasma pentraxin-3 was independently associated with a higher risk of mortality (RR 2.09) and major adverse cardiovascular events (RR 1.80) in patients with coronary artery disease.
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