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Updated: Dec 9, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Epidemiology of the inherited cardiomyopathies
William J McKenna1,2, Daniel P Judge3
1Institute of Cardiovascular Science, University College London, London, UK. w.mckenna@ucl.ac.uk.
Insights
Estimates for inherited cardiomyopathies like hypertrophic cardiomyopathy may be conservative. Many individuals with genetic variants show incomplete or late-onset disease, complicating genetic epidemiology.
Area of Science:
- Cardiology
- Genetics
- Epidemiology
Background:
- Current inherited cardiomyopathy prevalence estimates rely on screening studies, often in specific young adult groups.
- These estimates may be conservative, potentially underestimating disease burden.
- Genetic studies often focus on high-penetrance variants, potentially overlooking broader genetic contributions.
Purpose of the Study:
- To highlight challenges in defining the genetic epidemiology of inherited cardiomyopathies.
- To underscore the impact of incomplete and age-related disease expression on prevalence estimates.
- To address the limitations of current diagnostic and genetic study approaches.
Main Methods:
- Review of existing epidemiological and genetic literature on inherited cardiomyopathies.
- Analysis of diagnostic criteria and their impact on population estimates.
- Discussion of genetic variant penetrance and phenotypic variability.
Main Results:
- Global prevalence estimates for hypertrophic cardiomyopathy (1/500), dilated cardiomyopathy (1/250), and arrhythmogenic right ventricular cardiomyopathy (1/5,000) are likely conservative.
- A significant number of individuals with disease-causing variants exhibit incomplete or late-onset disease.
- Overlapping phenotypes, variable penetrance, and age-related expression complicate genetic epidemiology.
Conclusions:
- Accurate genetic epidemiology of cardiomyopathies is challenging due to incomplete/late expression and variable penetrance.
- Current estimates may underestimate the true prevalence of these conditions.
- Further research is needed to address diagnostic complexities and genetic variability.
Abstract:
In the absence of contemporary, population-based epidemiological studies, estimates of the incidence and prevalence of the inherited cardiomyopathies have been derived from screening studies, most often of young adult populations, to assess cardiovascular risk or to detect the presence of disease in athletes or military recruits. The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic right ventricular cardiomyopathy (1/5,000) are probably conservative given that only individuals who fulfil diagnostic criteria would have been included. This caveat is highly relevant because a substantial minority or even a majority of individuals who carry disease-causing genetic variants and are at risk of disease complications have incomplete and/or late-onset disease expression. The genetic literature on cardiomyopathy, which is often focused on the identification of genetic variants, has been biased in favour of pedigrees with higher penetrance. In clinical practice, an abnormal electrocardiogram with normal or non-diagnostic imaging results is a common finding for the sarcomere variants that cause hypertrophic cardiomyopathy, the titin and sarcomere variants that cause dilated cardiomyopathy and the desmosomal variants that cause either arrhythmogenic right ventricular cardiomyopathy or dilated cardiomyopathy. Therefore, defining the genetic epidemiology is also challenging given the overlapping phenotypes, incomplete and age-related expression, and highly variable penetrance even within individual families carrying the same genetic variant.
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Myocarditis I: Introduction
Cardiomyopathy V: Interprofessional Care

