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Pulsed Wave Doppler Assessment of Diastolic Dysfunction in the ZSF-1 Rat Model of Pulmonary Hypertension Due to Left Heart Disease
Published on: May 22, 2026
Time-course of diastolic dysfunction in different stages of chronic HCV related liver diseases
1Department of Medicine, Milano-Bicocca University Milan, Italy. epa.monza@libero.it
Insights
Hepatitis C virus (HCV) infection can cause heart abnormalities, including left ventricular wall thickening, even before cirrhosis develops. This early cardiac remodeling may worsen with advanced liver disease and portal hypertension.
Area of Science:
- Cardiology
- Hepatology
- Internal Medicine
Background:
- Advanced liver disease is associated with a hyperdynamic circulatory pattern.
- Cardiac dysfunction, including diastolic impairment, is observed in cirrhosis, historically attributed to ethanol toxicity.
- Early-stage cardiac changes in liver disease, particularly hepatitis C virus (HCV)-related, are less understood.
Purpose of the Study:
- To investigate the progression of diastolic dysfunction in different stages of HCV-related liver disease.
- To identify early cardiac structural changes in precirrhotic hepatitis C.
- To explore the role of HCV in cardiac abnormalities.
Main Methods:
- Echocardiography was used to assess left ventricular diastolic function and wall thickness.
- Patients with varying stages of HCV infection were studied.
- Liver biopsies were used to stage fibrosis.
Main Results:
- Diastolic function remains preserved in chronic hepatitis, but left ventricular wall thickening is evident in patients with fibrosis.
- Diastolic dysfunction patterns emerge in Child A and Child C cirrhotic patients, with greater wall thickness in Child A.
- Chronic aldosterone blockade shows potential benefits for cardiac remodeling in cirrhosis.
Conclusions:
- Increased left ventricular wall thickness in precirrhotic hepatitis C suggests a role for HCV in cardiac structural changes.
- These early cardiac abnormalities may act as co-factors in advanced cirrhosis.
- HCV-related cardiac remodeling can exacerbate the effects of portal hypertension on cardiovascular health.
Aim:
A hyperdynamic circulatory pattern in advanced liver disease is known since a long time. The first studies evaluating cardiac function in cirrhosis were performed in patients with alcoholic liver disease and thus this condition was attributed to the toxic effects of ethanol. A reduced performance of the left ventricle after physical and pharmacological strains along with an altered diastolic function has been demonstrated also in postviral cirrhosis. Many factors are involved in advanced cirrhosis whereas little is known in the earlier stages of disease.
Methods:
To this aim we have investigated patients with different stages of hepatitis C virus (HCV)-related liver disease to detect the time-course of diastolic dysfunction. An impaired relaxation and increased thickness of left ventricular walls along with an altered pattern of transmitral flow can be easily detected by means of echocardiography.
Results:
In chronic hepatitis diastolic function is preserved but increased thickness of left ventricle parietal walls can be detected in patients with fibrosis on liver biopsy. The typical pattern of diastolic dysfunction is observed in Child A cirrhotic patients and in Child C ascitic patients but thickness of parietal walls is more relevant in the former group. Chronic aldosterone blockade could exert favourable effects in heart remodeling suggesting a potential role of these drugs in cirrhotic cardiomyopathy.
Conclusions:
The presence of increased thickness of left ventricle parietal walls in chronic hepatitis C in the precirrhotic stage point to a putative role of HCV in this heart structural abnormality that can become a co-factor in the more advanced stages of cirrhosis when portal hypertension and its deleterious effects on systemic hemodynamics, cardiac function and structure become manifest.
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