# Cardiac Magnetic Resonance Imaging and Arrhythmic Risk Stratification in Cardiomyopathies

**Authors:** Gianluca Di Bella, Antonino Micari, Roberto Licordari, Pasquale Crea, Luigi Colarusso, Maurizio Cusmà-Piccione, Rocco Donato, Tommaso D’Angelo, Giuseppe Dattilo, Antonino Recupero, Cesare de Gregorio, Antonio Micari, Giovanni Donato Aquaro

PMC · DOI: 10.3390/jcm14144922 · 2025-07-11

## TL;DR

This review discusses how cardiac MRI helps assess arrhythmic risk in different types of cardiomyopathies beyond just measuring heart function.

## Contribution

The paper highlights the specific role of late gadolinium enhancement in predicting sudden cardiac death across different cardiomyopathy types.

## Key findings

- In dilated cardiomyopathy, LGE location predicts arrhythmic risk.
- In hypertrophic cardiomyopathy, LGE extent (>15%) correlates with higher cardiac death risk.
- In arrhythmogenic cardiomyopathy, LGE is more significant when combined with fat infiltration.

## Abstract

Cardiac magnetic resonance imaging (CMRI) has become an indispensable tool in evaluating arrhythmic risk and guiding therapeutic decisions in patients with non-ischemic cardiomyopathies (NICMs), including dilated (DCM), hypertrophic (HCM), and arrhythmogenic cardiomyopathies (ACM). Both European and American guidelines have given an additive and different value of late gadolinium enhancement (LGE) in specific morpho-functional (hypertrophic, dilated, and arrhythmogenic) phenotypes. In particular, LGE plays a different weight in relation to different cardiomyopathies. In dilated cardiomyopathy, LGE is able to predict arrhythmic risk in relationship to the presence and localization (septal and/or ring like LGE). On the contrary, in HCM, LGE is related to increased risk of cardiac death according to the extent (LGE >15%), while in ACM, it has a greater role in the presence of fat infiltration associated with LGE. In this review, we aim to identify predictors of sudden cardiac death related to myocardial structural features seen in CMRI in cardiomyopathies, going beyond the sole assessment of left ventricular function and ejection fraction.

## Linked entities

- **Diseases:** dilated cardiomyopathy (MONDO:0005021), hypertrophic cardiomyopathy (MONDO:0005045)

## Full-text entities

- **Diseases:** ACM (MESH:D019571), cardiac death (MESH:D003643), Cardiomyopathies (MESH:D009202), Arrhythmic (OMIM:212500), sudden cardiac death (MESH:D016757), dilated (MESH:D002311), hypertrophic (MESH:D002312), HCM (MESH:D000092183)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12295573/full.md

---
Source: https://tomesphere.com/paper/PMC12295573