Key result
CMR-derived epicardial adipose tissue heterogeneity strongly predicts post-MI ventricular and atrial arrhythmias.
Why the study?
Does CMR-quantified epicardial adipose tissue heterogeneity predict ventricular and atrial arrhythmias in post-myocardial infarction patients?
Cohort (n=241)
No
Does CMR-quantified epicardial adipose tissue heterogeneity predict ventricular and atrial arrhythmias in post-myocardial infarction patients?
p-value: p=<0.001
CMR-quantified epicardial adipose tissue heterogeneity (entropy) serves as an independent predictor of both ventricular and atrial arrhythmias following myocardial infarction, enhancing risk stratification.
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May refine post-MI arrhythmia risk stratification beyond LVEF; hypothesis-generating and requires prospective validation before clinical use.
BACKGROUND: Epicardial adipose tissue (EAT) contributes to arrhythmogenic substrate development through electrophysiological and structural remodeling. Pathological EAT exhibits significant heterogeneity. We investigated whether EAT heterogeneity, quantified by entropy analysis on cardiac magnetic resonance (CMR), predicts the occurrence of ventricular and atrial arrhythmias post-myocardial infarction (MI). MATERIALS AND METHODS: This cohort study enrolled 241 consecutive patients post-MI. CMR was performed to assess EAT volume, myocardial scar, biventricular function, and strain. EAT heterogeneity was quantified using an entropy algorithm. The primary endpoints were the occurrence of ventricular arrhythmias (VAs) or atrial tachyarrhythmias (AAs). RESULTS: Over a median follow-up of 31 months, 43 (17.8%) patients developed VAs and 30 (12.4%) developed AAs. EAT entropy was significantly higher in patients who developed either VAs or AAs. In multivariable Cox regression analysis, EAT entropy, LA reservoir strain (Es), and global longitudinal strain (GLS) were independent predictors of VAs. For AAs, EAT entropy, Es, and EAT thickness independently predicted the outcome. ROC analysis revealed that the model integrating these parameters have good efficacy for the prognosis evaluation of VAs (area under the curve [AUC] = 0.872) and AAs (AUC = 0.917). Myocardial fibrosis exhibited modest correlations with EAT entropy. CONCLUSION: EAT heterogeneity, quantified by entropy, is an independent predictor of both VAs and AAs in post-MI patients. This novel imaging biomarker may enhance risk stratification and guide therapeutic strategies in this high-risk population.
Zhao et al. (2026) conducted a cohort in Myocardial infarction (n=241). Epicardial adipose tissue (EAT) heterogeneity vs. Lower EAT heterogeneity was evaluated on Occurrence of ventricular arrhythmias (VAs) or atrial tachyarrhythmias (AAs) (p=<0.001). Epicardial adipose tissue heterogeneity, quantified by entropy on cardiac magnetic resonance, independently predicted the occurrence of ventricular (AUC 0.872) and atrial arrhythmias (AUC 0.917) in post-myocardial infarction patients.
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