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Published on: August 8, 2022
The Feline Cardiomyopathies: 2. Hypertrophic cardiomyopathy
Mark D Kittleson1, Etienne Côté2
1School of Veterinary Medicine, Department of Medicine and Epidemiology, University of California, Davis, and Veterinary Information Network, 777 West Covell Boulevard, Davis, CA 95616, USA.
Insights
Hypertrophic cardiomyopathy (HCM) in cats is common but often subclinical. Severe cases can lead to heart failure or arterial thromboembolism (ATE), with a poor prognosis despite treatment.
Area of Science:
- Veterinary Cardiology
- Feline Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is the most prevalent feline cardiomyopathy, affecting up to 15% of domestic cats, often subclinically.
- While severe forms leading to heart failure or arterial thromboembolism (ATE) are less common, they significantly impact prognosis.
Purpose of the Study:
- To summarize the clinical presentation, diagnosis, and management of feline hypertrophic cardiomyopathy.
- To highlight the challenges in diagnosing and treating this complex cardiac condition in cats.
Main Methods:
- Review of clinical data and diagnostic approaches for feline HCM.
- Analysis of pathological mechanisms, including systolic anterior motion of the mitral valve (SAM) and diastolic dysfunction.
- Evaluation of current treatment strategies for heart failure and ATE prevention.
Main Results:
- Feline HCM affects cats of all ages, breeds, and sexes, with higher prevalence in males and domestic shorthairs.
- Diagnosis can be challenging, especially for mild to moderate cases, often requiring exclusion of other conditions.
- Diastolic dysfunction is the primary driver of clinical signs, with treatments targeting heart failure and ATE prevention.
Conclusions:
- Most cats with HCM remain asymptomatic, but a significant minority develop severe clinical signs with a poor prognosis.
- The underlying cause of HCM in most cats remains unknown, and current treatments do not reverse or slow the disease progression.
Practical Relevance:
Hypertrophic cardiomyopathy (HCM) is the most common form of feline cardiomyopathy observed clinically and may affect up to approximately 15% of the domestic cat population, primarily as a subclinical disease. Fortunately, severe HCM, leading to heart failure or arterial thromboembolism (ATE), only occurs in a small proportion of these cats.
Patient Group:
Domestic cats of any age from 3 months upward, of either sex and of any breed, can be affected. A higher prevalence in male and domestic shorthair cats has been reported.
Diagnostics:
Subclinical feline HCM may or may not produce a heart murmur or gallop sound. Substantial left atrial enlargement can often be identified radiographically in cats with severe HCM. Biomarkers should not be relied on solely to diagnose the disease. While severe feline HCM can usually be diagnosed via echocardiography alone, feline HCM with mild to moderate left ventricular (LV) wall thickening is a diagnosis of exclusion, which means there is no definitive test for HCM in these cats and so other disorders that can cause mild to moderate LV wall thickening (eg, hyperthyroidism, systemic hypertension, acromegaly, dehydration) need to be ruled out.
Key Findings:
While a genetic cause of HCM has been identified in two breeds and is suspected in another, for most cats the cause is unknown. Systolic anterior motion of the mitral valve (SAM) is the most common cause of dynamic left ventricular outflow tract obstruction (DLVOTO) and, in turn, the most common cause of a heart murmur with feline HCM. While severe DLVOTO is probably clinically significant and so should be treated, lesser degrees probably are not. Furthermore, since SAM can likely be induced in most cats with HCM, the distinction between HCM without obstruction and HCM with obstruction (HOCM) is of limited importance in cats. Diastolic dysfunction, and its consequences of abnormally increased atrial pressure leading to signs of heart failure, and sluggish atrial blood flow leading to ATE, is the primary abnormality that causes clinical signs and death in affected cats. Treatment (eg, loop diuretics) is aimed at controlling heart failure. Preventive treatment (eg, antithrombotic drugs) is aimed at reducing the risk of complications (eg, ATE).
Conclusions:
Most cats with HCM show no overt clinical signs and live a normal or near-normal life despite this disease. However, a substantial minority of cats develop overt clinical signs referable to heart failure or ATE that require treatment. For most cats with clinical signs caused by HCM, the long-term prognosis is poor to grave despite therapy.
Areas Of Uncertainty:
Genetic mutations (variants) that cause HCM have been identified in a few breeds, but, despite valiant efforts, the cause of HCM in the vast majority of cats remains unknown. No treatment currently exists that reverses or even slows the cardiomyopathic process in HCM, again despite valiant efforts. The search goes on.
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