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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Hypertrophic cardiomyopathy
Murillo de Oliveira Antunes1,2, Thiago Luis Scudeler1
1Instituto do Coração (InCor), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Insights
Hypertrophic cardiomyopathy (HCM) is a common inherited heart condition with varied outcomes. This review covers clinical issues and treatment options for managing HCM symptoms and progression.
Area of Science:
- Cardiology
- Genetics
- Internal Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited cardiac disease.
- HCM presents with diverse clinical manifestations, from asymptomatic cases to severe heart failure or sudden cardiac death.
- Left ventricular hypertrophy and altered ventricular shape often lead to dynamic left ventricular outflow obstruction.
Purpose of the Study:
- To review the key clinical issues associated with hypertrophic cardiomyopathy.
- To summarize current pharmacological and therapeutic interventions for HCM.
- To provide an overview of treatment strategies aimed at symptom alleviation and disease management.
Main Methods:
- Literature review of clinical issues in hypertrophic cardiomyopathy.
- Summary of current pharmacotherapies for HCM.
- Overview of septal reduction therapies for HCM.
Main Results:
- HCM is characterized by significant variability in presentation and progression.
- Dynamic left ventricular outflow obstruction is common in HCM patients.
- Pharmacological therapies and septal reduction therapies are primary treatment modalities.
Conclusions:
- Effective management of HCM requires addressing its variable nature and potential complications.
- Treatment goals focus on alleviating symptoms and improving the natural history of the disease.
- A comprehensive understanding of clinical issues and treatment options is crucial for HCM patient care.
Abstract:
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. The disease is characterized by marked variability in morphological expression and natural history, ranging from asymptomatic to heart failure or sudden cardiac death. Left ventricular hypertrophy and abnormal ventricular configuration result in dynamic left ventricular outflow obstruction in most patients. The goal of pharmacological therapy in HCM is to alleviate the symptoms, and it includes pharmacotherapies and septal reduction therapies. In this review, we summarize the relevant clinical issues and treatment options of HCM.
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