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Published on: January 28, 2020
[Prognostic value of tumor necrosis factor-alpha in patients with ST-segment elevation acute myocardial infarction]
Manuel Gonzálvez1, José A Ruiz-Ros, Matías Pérez-Paredes
1Unidad de Cardiología, Hospital General Universitario J.M. Morales Meseguer, Murcia, España. mgonzalvez@smcardiologia.es
Insights
Tumor necrosis factor-alpha (TNFalpha) and C-reactive protein (CRP) levels predict cardiovascular events in ST-elevation myocardial infarction (STEMI) patients. Elevated TNFalpha 48 hours post-STEMI indicates higher risk.
Area of Science:
- Cardiovascular Medicine
- Inflammation Biology
- Biomarker Discovery
Context:
- ST-segment elevation myocardial infarction (STEMI) is a critical cardiovascular event.
- Identifying reliable prognostic biomarkers is crucial for managing STEMI patients.
- Inflammatory markers play a significant role in post-myocardial infarction complications.
Purpose:
- To evaluate the prognostic value of Tumor Necrosis Factor-alpha (TNFalpha) in STEMI patients.
- To assess the predictive capability of TNFalpha and other inflammatory markers for cardiovascular events at six-month follow-up.
Summary:
- This study measured TNFalpha, C-reactive protein (CRP), and interleukin-6 levels in 74 STEMI patients.
- Higher TNFalpha levels at 48 hours post-symptom onset were associated with increased risk of ischemic events, heart failure, and overall cardiovascular events.
- Both plasma TNFalpha levels at 48 hours and CRP levels at admission independently predicted cardiovascular events in STEMI patients.
Impact:
- Findings highlight TNFalpha as a valuable prognostic biomarker in STEMI.
- Early identification of high-risk patients can guide timely therapeutic interventions.
- This research contributes to understanding the inflammatory cascade in acute myocardial infarction.
Introduction And Objectives:
Tumor necrosis factor-alpha (TNFalpha in patients with ST-segment elevation myocardial infarction (STEMI). The aim of this study was to determine the prognostic value of TNFalpha in this clinical setting at six-month follow-up.
Methods:
The levels of TNFalpha, C-reactive protein (CRP), interleukin 6 and type 1 soluble intercellular adhesion molecules measured within the first 10 h of symptom onset and at 48 h in 74 consecutive patients admitted with STEMI. The relationships between these levels and the incidence of ischemic events (i.e., angina, reinfarction, and death), heart failure (HF), or both (i.e., all cardiovascular events) were studied.
Results:
Overall, TNFalpha levels were significantly higher in patients who had an ischemic event or HF than in those who did not (P<.02 for both). At 48 h, the adjusted odds ratios of those in the highest TNFalpha quartile (2.92 pg/mL) for the development of ischemic events, HF, and all cardiovascular events combined were 13.1, 9.59 and 9.75, respectively. A TNFalpha level of 2.04 pg/mL at 48 h had a sensitivity of 78% and a specificity of 72.5% in predicting a cardiovascular event of any form. The CRP level, but not the TNFalpha level, at admission was found to be an independent predictor of the development of a cardiovascular events.
Conclusions:
In patients with STEMI, the plasma TNFalpha level 48 h after symptom onset and the CRP level at admission were independent predictors of cardiovascular events.
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