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Published on: April 27, 2016
Association of epicardial and intramyocardial fat with ventricular arrhythmias
Maryam Mojarrad Sani1, Eric Sung2, Marc Engels1
1Department of Medicine, Division of Cardiology, Johns Hopkins Hospital, Baltimore, Maryland.
Insights
Myocardial fat volume and distribution are linked to ventricular arrhythmias (VA) in cardiomyopathy patients. The association differs between ischemic cardiomyopathy (ICM) and nonischemic cardiomyopathy (NICM) patients, highlighting substrate-specific risks.
Area of Science:
- Cardiology
- Medical Imaging
- Biomedical Engineering
Background:
- Myocardial fibrosis increases ventricular arrhythmia (VA) risk in ischemic (ICM) and nonischemic (NICM) cardiomyopathy.
- Myocardial fat accumulation is increasingly recognized as a contributor to ventricular arrhythmogenesis.
- The specific roles of epicardial adipose tissue and intramyocardial fat in VA remain unclear.
Purpose of the Study:
- To evaluate the association between contrast-enhanced computed tomography (CE-CT) derived left ventricular (LV) tissue heterogeneity, epicardial adipose tissue volume, and intramyocardial fat volume with VA risk.
- To differentiate these associations in patients with ICM versus NICM.
Main Methods:
- Utilized data from the PROSE-ICD registry, including patients who underwent CE-CT.
- Quantified intramyocardial fat volume (-180 to -5 HU), epicardial adipose tissue volume (-200 to -50 HU), and LV tissue heterogeneity.
- Assessed the primary endpoint of appropriate implantable cardioverter-defibrillator (ICD) shocks or sudden arrhythmic death.
Main Results:
- LV tissue heterogeneity correlated with VA risk (OR 1.10, P = .01), particularly in the ICM cohort.
- In NICM patients, both epicardial adipose tissue (OR 1.11, P = .01) and intramyocardial fat volume (OR 1.21, P = .01) were associated with VA.
- These fat-related associations were not significant in the ICM cohort (P > .19 for both).
Conclusions:
- Increased fat distribution heterogeneity is linked to VA in ICM patients.
- In NICM patients, greater intramyocardial and epicardial fat volumes predict higher VA risk.
- The contribution of cardiac fat to VA appears dependent on the underlying cardiomyopathy substrate.
Background:
Among patients with ischemic cardiomyopathy (ICM) and nonischemic cardiomyopathy (NICM), myocardial fibrosis is associated with an increased risk for ventricular arrhythmia (VA). Growing evidence suggests that myocardial fat contributes to ventricular arrhythmogenesis. However, little is known about the volume and distribution of epicardial adipose tissue and intramyocardial fat and their relationship with VAs.
Objective:
The purpose of this study was to assess the association of contrast-enhanced computed tomography (CE-CT)-derived left ventricular (LV) tissue heterogeneity, epicardial adipose tissue volume, and intramyocardial fat volume with the risk of VA in ICM and NICM patients.
Methods:
Patients enrolled in the PROSE-ICD registry who underwent CE-CT were included. Intramyocardial fat volume (voxels between -180 and -5 Hounsfield units [HU]), epicardial adipose tissue volume (between -200 and -50 HU), and LV tissue heterogeneity were calculated. The primary endpoint was appropriate ICD shocks or sudden arrhythmic death.
Results:
Among 98 patients (47 ICM, 51 NICM), LV tissue heterogeneity was associated with VA (odds ratio [OR] 1.10; P = .01), particularly in the ICM cohort. In the NICM subgroup, epicardial adipose tissue and intramyocardial fat volume were associated with VA (OR 1.11, P = .01; and OR = 1.21, P = .01, respectively) but not in the ICM patients (OR 0.92, P =.22; and OR = 0.96, P =.19, respectively).
Conclusion:
In ICM patients, increased fat distribution heterogeneity is associated with VA. In NICM patients, an increased volume of intramyocardial fat and epicardial adipose tissue is associated with a higher risk for VA. Our findings suggest that fat's contribution to VAs depends on the underlying substrate.
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