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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Paradigm of Sudden Death Prevention in Hypertrophic Cardiomyopathy
Barry J Maron1, Ethan J Rowin1, Martin S Maron1
1From the HCM Institute, Division of Cardiology, Tufts Medical Center, Boston, MA.
Insights
Implantable cardioverter-defibrillators (ICDs) significantly reduce sudden cardiac death in hypertrophic cardiomyopathy (HCM) patients. An enhanced risk model improves patient selection for primary prevention ICDs, saving lives.
Area of Science:
- Cardiology
- Genetics
- Electrophysiology
Background:
- Hypertrophic cardiomyopathy (HCM) is a primary genetic heart disease and a leading cause of sudden cardiac death in young individuals.
- The widespread adoption of implantable cardioverter-defibrillators (ICDs) necessitates precise patient selection for primary prevention.
Purpose of the Study:
- To evaluate the effectiveness of an enhanced risk stratification algorithm for selecting hypertrophic cardiomyopathy patients for primary prevention ICD implantation.
- To assess the impact of ICD therapy on overall mortality in the HCM population.
Main Methods:
- Development and prospective application of an enhanced risk stratification algorithm incorporating contemporary markers, including contrast-magnetic resonance imaging findings like left ventricular apical aneurysm.
- Comparison of the enhanced algorithm's sensitivity against the European Society of Cardiology's risk score model for identifying high-risk patients.
Main Results:
- The enhanced algorithm demonstrated 95% sensitivity in identifying patients requiring appropriate ICD therapies for ventricular arrhythmias.
- ICD therapy reduced overall HCM-related mortality to 0.5% annually, irrespective of patient age.
- The number needed to treat with ICDs to prevent one death from lethal ventricular tachyarrhythmias was 6:1.
- The European Society of Cardiology model showed only 33% sensitivity in identifying high-risk patients.
Conclusions:
- The introduction of ICDs, coupled with a refined risk stratification algorithm, has transformed HCM management.
- This approach significantly reduces HCM-related mortality and the risk of sudden arrhythmic death, improving patient outcomes.
- The enhanced algorithm offers superior accuracy in identifying candidates for primary prevention ICDs compared to existing models.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a worldwide genetic heart disease and a common cause of sudden death in the young. Penetration of the implantable cardioverter-defibrillator (ICD) into this patient population over the past 20 years has made accurate selection of patients for primary prevention ICDs a priority. Consequently, a new paradigm has emerged in the management of this complex disease with ICD therapy responsible for a substantial decrease in overall HCM-related mortality (to 0.5%/y) and independent of patient age. Selection of candidates for ICDs has matured substantially with the formulation of an enhanced risk stratification algorithm. One or more contemporary risk markers judged major within a given patient's clinical profile, in association with physician judgment and shared decision-making, is sufficient to consider a primary prevention ICD implant. An enhanced American College of Cardiology/American Heart Association risk factor model (including new contrast-magnetic resonance-based markers, such as left ventricular apical aneurysm) used prospectively to make ICD decisions proved to be 95% sensitive for identifying patients who would experience ≥1 appropriate device therapies terminating ventricular tachycardia/fibrillation. The number of HCM patients required to treat with ICDs to save 1 patient with abolition of lethal ventricular tachyarrhythmias was 6:1, similar to randomized defibrillator trials in other cardiomyopathies. In contrast to patients with ischemic heart disease, after ICD shock HCM patients rarely experience transformation to heart failure deterioration or sudden arrhythmic death. The mathematically derived risk score model proposed by the European Society of Cardiology was inferior for identifying high-risk patients susceptible to arrhythmic sudden death with a sensitivity of only 33%, leaving many patients exposed to the possibility of sudden death without ICDs. In conclusion, introduction of the ICD associated with a matured risk stratification algorithm has altered management strategy and clinical course of many HCM patients, making the likelihood of sudden death prevention a reality and fulfilling the aspiration of preservation of life and reduced mortality for this vulnerable patient population.
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