Related Experiment Video
Updated: Feb 3, 2026

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Towards cardiac MRI based risk stratification in idiopathic dilated cardiomyopathy
Pamela Frances Brown1, Chris Miller1, Andrea Di Marco2
1Cardiac MRI Department, North West Heart Centre, Manchester University Foundation Trust-Wythenshawe Site, Manchester, UK.
Insights
Sudden cardiac death (SCD) risk in dilated cardiomyopathy (DCM) needs better prediction. Cardiac MRI offers advanced imaging beyond ejection fraction to identify patients who would benefit most from an implantable cardiac defibrillator (ICD).
Area of Science:
- Cardiology
- Medical Imaging
- Biomarkers
Background:
- Sudden cardiac death (SCD) risk persists in dilated cardiomyopathy (DCM) patients, even with current implantable cardiac defibrillator (ICD) selection criteria.
- Current guidelines for ICD implantation in DCM, based on ejection fraction (EF) <35%, are insufficient as most SCD events occur in patients with EF >35%.
Purpose of the Study:
- To evaluate the role of Cardiac Magnetic Resonance (CMR) imaging in improving risk stratification for SCD in DCM patients.
- To explore advanced CMR techniques beyond EF for identifying fibrosis and predicting outcomes.
Main Methods:
- Utilizing Cardiac Magnetic Resonance (CMR) for ejection fraction (EF) calculation and detailed myocardial tissue characterization.
- Assessing late gadolinium enhancement (LGE) for focal fibrosis detection.
- Investigating T1 mapping and extracellular volume (ECV) calculation for diffuse myocardial fibrosis assessment.
Main Results:
- Late gadolinium enhancement (LGE) identifies mid-wall fibrosis in approximately 30% of DCM patients, strongly associated with increased SCD risk.
- Elevated ECV and native T1 values are linked to adverse outcomes, though their direct relationship with SCD requires further study.
- CMR offers incremental value over EF for risk stratification in DCM.
Conclusions:
- Standard EF criteria are inadequate for selecting DCM patients for primary prevention ICDs.
- CMR, through techniques like LGE, T1 mapping, and ECV, provides superior risk stratification for SCD in DCM.
- Further research is needed, but CMR tools can optimize patient selection, improve outcomes, and enhance resource utilization in DCM management.
Abstract:
Sudden cardiac death (SCD) secondary to arrhythmia remains a risk in those with dilated cardiomyopathy (DCM), an implantable cardiac defibrillator (ICD) is an effective strategy to prevent SCD. Current guidelines recommend selection for ICD based on ejection fraction (EF) less than 35%, however, most SCD occurs in those with EF>35%. Although meta-analysis has demonstrated a survival benefit for primary prevention ICD in DCM, no randomised trial has shown a significant reduction in overall mortality including the most recent 'Danish Study to Assess the Efficacy of ICDs in Patients With Non-Ischemic Systolic Heat Failure on Mortality' study. Clearly, a more sophisticated selection strategy is required. Cardiac MRI (CMR) is an ideal non-invasive imaging technique which allows calculation of EF as well as tissue characterisation with gadolinium contrast, parametric mapping and feature tracking. Late gadolinium enhancement detects mid-wall fibrosis in approximately 30% of those with DCM, three meta-analyses have demonstrated an association between fibrosis in DCM and SCD, and those without fibrosis are at low risk of SCD. T1 mapping and extracellular volume (ECV) calculation are methods of demonstrating diffuse fibrosis in the myocardium. Raised ECV and native T1 have been associated with worse outcomes but the relationship to SCD has not been well studied. Undoubtedly, more research is required but CMR has several tools which offer incremental value above EF to improve risk stratification and consequent outcomes and resource utilisation in those with DCM.
More Related Videos
Related Concept Videos
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy VI: Nursing Management

