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Early Inflammatory Biomarkers, Ventricular Dysfunction and In-Hospital Mortality in Patients with ST-Elevation
Dan Claudiu Magureanu1,2, Maria Luiza Hiceag3,4, Camelia Bianca Rus5,6,7
1Department of Pharmacology, Toxicology and Clinical Pharmacology, Iuliu Hatieganu University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
Insights
In ST-elevation myocardial infarction (STEMI) patients treated with primary PCI, inflammatory biomarkers reflect injury severity but don't predict short-term mortality. Age, ventricular dysfunction, and residual coronary disease are key mortality predictors.
Area of Science:
- Cardiology
- Biomarkers
- Inflammation
Background:
- Inflammation is key in ST-elevation myocardial infarction (STEMI) pathophysiology.
- Routine inflammatory biomarkers may predict outcomes in primary percutaneous coronary intervention (PCI) patients.
Purpose of the Study:
- Evaluate associations between admission inflammatory biomarkers, ventricular dysfunction, and in-hospital mortality in STEMI patients undergoing primary PCI.
Main Methods:
- Retrospective observational study of 600 STEMI patients treated with primary PCI.
- Measured C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and C-reactive protein-to-lymphocyte ratio (CLR).
- Used multivariable logistic regression to identify mortality predictors.
Main Results:
- In-hospital mortality was 9.0%.
- Reduced left ventricular ejection fraction (LVEF ≤ 40%) correlated with higher CRP and CLR.
- Inflammatory biomarkers associated with ventricular dysfunction but did not independently predict mortality.
Conclusions:
- Early mortality in STEMI patients post-PCI is driven by age, ventricular dysfunction, and residual coronary disease.
- Inflammatory biomarkers indicate myocardial injury severity rather than independently predicting short-term mortality.
Abstract:
Background/Objectives: Inflammation plays a central role in the pathophysiology of ST-elevation myocardial infarction (STEMI) and may influence myocardial injury, ventricular dysfunction and clinical outcomes. Simple inflammatory biomarkers derived from routine laboratory tests have been proposed as potential prognostic indicators in patients undergoing primary percutaneous coronary intervention (PCI). Objective: This study aimed to evaluate the association between admission inflammatory biomarkers, echocardiographic markers of ventricular dysfunction and in-hospital mortality in patients with STEMI treated with primary PCI. Methods: We conducted a retrospective observational study including 600 consecutive patients admitted with STEMI and treated with primary PCI between January 2021 and August 2025. Inflammatory biomarkers measured at admission included C-reactive protein (CRP); neutrophil-to-lymphocyte ratio (NLR); platelet-to-lymphocyte ratio (PLR); systemic immune-inflammation index (SII) and C-reactive protein-to-lymphocyte ratio (CLR). Echocardiographic parameters and clinical outcomes were recorded. Multivariable logistic regression analysis was performed to identify independent predictors of in-hospital mortality. Results: In-hospital mortality occurred in 54 patients (9.0%). Patients with reduced left ventricular ejection fraction (LVEF ≤ 40%) had significantly higher CRP and CLR levels (p < 0.01). Inflammatory biomarkers were associated with markers of ventricular dysfunction but were not independent predictors of mortality. Age, LVEF < 40% and the number of residual coronary lesions independently predicted in-hospital death. Conclusions: In STEMI patients undergoing primary PCI, early mortality is mainly determined by age; ventricular dysfunction and residual coronary disease burden, while inflammatory biomarkers primarily reflect the severity of myocardial injury rather than independently predicting short-term mortality.
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