Related Experiment Video
Updated: May 7, 2026

Histological Quantification of Chronic Myocardial Infarct in Rats
Published on: December 11, 2016
Relation between white blood cell count and final infarct size in patients with ST-segment elevation acute myocardial
Tullio Palmerini1, Sorin J Brener, Philippe Genereux
1Dipartimento Cardiovascolare, Policlinico S. Orsola, Bologna, Italy.
Insights
Elevated white blood cell count (WBCc) in ST-segment elevation myocardial infarction (STEMI) patients predicts larger heart attack size. This finding suggests WBCc may be a key factor in STEMI outcomes, impacting infarct size measured by cardiac MRI.
Area of Science:
- Cardiology
- Biomedical Imaging
- Inflammation Research
Background:
- Elevated white blood cell count (WBCc) is linked to cardiac mortality in ST-segment elevation myocardial infarction (STEMI).
- The mechanisms connecting WBCc to adverse cardiac events in STEMI remain unclear.
- Understanding this relationship is crucial for improving STEMI patient management.
Purpose of the Study:
- To investigate the association between admission WBCc and infarct size in STEMI patients.
- To determine if WBCc is an independent predictor of infarct size.
- To utilize cardiac magnetic resonance imaging (CMR) for precise infarct size measurement.
Main Methods:
- Analysis of data from the INFUSE AMI trial, including 407 STEMI patients.
- Stratification of patients into tertiles based on admission WBCc.
- Measurement of infarct size using CMR 30 days post-primary percutaneous coronary intervention.
Main Results:
- A significant, stepwise increase in infarct size was observed across increasing tertiles of WBCc (p <0.0001).
- Absolute infarct mass and abnormal wall motion scores also increased with higher WBCc.
- Multivariate analysis confirmed WBCc as an independent predictor of infarct size.
Conclusions:
- Elevated admission WBCc is a strong, independent predictor of infarct size in anterior wall STEMI patients.
- This association is evident even after primary percutaneous coronary intervention.
- WBCc may play a significant role in determining myocardial damage extent post-STEMI.
Abstract:
Although it has been shown that elevated white blood cell count (WBCc) on presentation is associated with an increased risk of cardiac mortality in patients with ST-segment elevation myocardial infarction (STEMI), the responsible mechanisms are unknown. We therefore sought to investigate whether elevated WBCc is associated with increased infarct size measured with cardiac magnetic resonance imaging 30 days after primary percutaneous coronary intervention in the Intracoronary Abciximab and Aspiration Thrombectomy in Patients With Large Anterior Myocardial Infarction trial. INFUSE AMI randomized patients with STEMI and proximal or mid-left anterior descending coronary artery occlusion to bolus intracoronary abciximab versus no abciximab and to manual aspiration versus no aspiration. WBCc at hospital admission was available in 407 of 452 randomized patients. Patients were stratified according to tertiles of WBCc. At 30 days, a significant stepwise increase in infarct size (percentage of total left ventricular mass) was apparent across tertiles of increasing WBCc (median [interquartile range] for tertiles I vs II vs III = 11.2% [3.8% to 19.6%] vs 17.5% [0.5% to 22.9%] vs 19.1% [13.7 to 26.0], respectively, p <0.0001). Absolute infarct mass in grams and abnormal wall motion score were also significantly increased across tertiles of WBC. By multivariate linear regression analysis, WBCc was an independent predictor of infarct size along with intracoronary abciximab randomization, age, time from symptom onset to first device, proximal left anterior descending location, and baseline TIMI flow of 0/1. In conclusion, in patients with anterior wall STEMI, an elevated admission WBCc is a powerful independent predictor of infarct size measured with cardiac magnetic resonance imaging 30 days after primary percutaneous coronary intervention.
Related Concept Videos
Acute Coronary Syndrome I: Introduction
Acute Coronary Syndrome III: Diagnostic Studies

