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Published on: August 8, 2022
Cirrhotic cardiomyopathy
Soon Koo Baik1, Tamer R Fouad, Samuel S Lee
1Dept of Medicine, Yonsei University Wonju College of Medicine, Wonju, South Korea. baiksk@yonsei.ac.kr
Insights
Cirrhotic cardiomyopathy, a heart condition in cirrhosis patients, presents latent dysfunction worsened by stress. Early diagnosis and supportive care are crucial for managing this condition.
Area of Science:
- Cardiology
- Hepatology
- Internal Medicine
Background:
- Cirrhotic cardiomyopathy (CC) describes cardiac dysfunction in cirrhosis patients.
- It involves systolic/diastolic dysfunction, electrophysiological changes, and structural alterations.
- CC is often latent, manifesting under physiological or pharmacological stress.
Purpose of the Study:
- To define cirrhotic cardiomyopathy and its clinical features.
- To explore its pathogenesis and diagnostic approaches.
- To review current management and prognosis.
Main Methods:
- Literature review of cirrhotic cardiomyopathy.
- Analysis of clinical features, diagnostic methods, and pathogenic mechanisms.
- Evaluation of management strategies and prognosis.
Main Results:
- CC features include increased cardiac output, attenuated contractility/relaxation under stress, and prolonged QT intervals.
- Diastolic dysfunction typically precedes systolic dysfunction.
- Stresses like liver transplantation or TIPS can unmask latent CC, potentially leading to overt heart failure.
Conclusions:
- Cirrhotic cardiomyopathy is a significant complication of cirrhosis with multifactorial pathogenesis.
- Diagnosis requires careful assessment, including stress testing.
- Management is largely supportive, with potential for reversibility; further research is needed.
Abstract:
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. The prevalence of cirrhotic cardiomyopathy remains unknown at present, mostly because the disease is generally latent and shows itself when the patient is subjected to stress such as exercise, drugs, hemorrhage and surgery. The main clinical features of cirrhotic cardiomyopathy include baseline increased cardiac output, attenuated systolic contraction or diastolic relaxation in response to physiologic, pharmacologic and surgical stress, and electrical conductance abnormalities (prolonged QT interval). In the majority of cases, diastolic dysfunction precedes systolic dysfunction, which tends to manifest only under conditions of stress. Generally, cirrhotic cardiomyopathy with overt severe heart failure is rare. Major stresses on the cardiovascular system such as liver transplantation, infections and insertion of transjugular intrahepatic portosystemic stent-shunts (TIPS) can unmask the presence of cirrhotic cardiomyopathy and thereby convert latent to overt heart failure. Cirrhotic cardiomyopathy may also contribute to the pathogenesis of hepatorenal syndrome. Pathogenic mechanisms of cirrhotic cardiomyopathy are multiple and include abnormal membrane biophysical characteristics, impaired beta-adrenergic receptor signal transduction and increased activity of negative-inotropic pathways mediated by cGMP. Diagnosis and differential diagnosis require a careful assessment of patient history probing for excessive alcohol, physical examination for signs of hypertension such as retinal vascular changes, and appropriate diagnostic tests such as exercise stress electrocardiography, nuclear heart scans and coronary angiography. Current management recommendations include empirical, nonspecific and mainly supportive measures. The exact prognosis remains unclear. The extent of cirrhotic cardiomyopathy generally correlates to the degree of liver insufficiency. Reversibility is possible (either pharmacological or after liver transplantation), but further studies are needed.
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