Right Heart Remodeling in Patients with End-Stage Alcoholic Liver Cirrhosis: Speckle Tracking Point of View
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Updated: Jan 20, 2026

Transthoracic Speckle Tracking Echocardiography for the Quantitative Assessment of Left Ventricular Myocardial Deformation
Published on: October 20, 2016
Kun Zhang1, Alexander Braun1, Francisca von Koeckritz1
1Department of Internal Medicine and Cardiology, Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Insights
Alcoholic liver cirrhosis patients show right atrial and right ventricular remodeling despite preserved systolic function. Liver enzymes, bilirubin, and MELD scores correlate with this cardiac remodeling.
Area of Science:
- Cardiology
- Hepatology
- Medical Imaging
Background:
- Cardiac remodeling data in alcoholic liver cirrhosis is limited.
- Investigated right atrial (RA) and right ventricular (RV) structure, function, and mechanics in these patients.
Purpose of the Study:
- To investigate cardiac remodeling in patients with alcoholic liver cirrhosis.
- To assess RA and RV structure, function, and mechanics using echocardiography.
Main Methods:
- Retrospective cross-sectional study of 67 cirrhotic patients and 36 healthy controls.
- Echocardiographic examination including offline strain analysis was performed.
Main Results:
- Patients with cirrhosis had increased RV basal diameter and thickness but preserved RV systolic function.
- Significantly lower global, endocardial, and epicardial RV longitudinal strains were observed in cirrhotic patients.
- RA active function was higher, but reservoir and conduit strains were lower in cirrhotic patients. Transaminases, bilirubin, and MELD score correlated with RV and RA remodeling parameters.
Conclusions:
- Right atrial and right ventricular remodeling are present in end-stage alcoholic liver cirrhosis.
- RV systolic function is preserved despite remodeling.
- Liver enzymes, bilirubin, and MELD score are associated with RV and RA remodeling.
Background:
Data regarding cardiac remodeling in patients with alcoholic liver cirrhosis are scarce. We sought to investigate right atrial (RA) and right ventricular (RV) structure, function, and mechanics in patients with alcoholic liver cirrhosis.
Methods:
This retrospective cross-sectional investigation included 67 end-stage cirrhotic patients, who were referred for evaluation for liver transplantation and 36 healthy controls. All participants underwent echocardiographic examination including strain analysis, which was performed offline.
Results:
RV basal diameter and RV thickness were significantly higher in patients with cirrhosis. Conventional parameters of the RV systolic function were similar between the observed groups. Global, endocardial, and epicardial RV longitudinal strains were significantly lower in patients with cirrhosis. Active RA function was significantly higher in cirrhotic patients than in controls. The RA reservoir and conduit strains were significantly lower in cirrhotic patients, while there was no difference in the RA contractile strain. Early diastolic and systolic RA strain rates were significantly lower in cirrhotic patients than in controls, whereas there was no difference in the RA late diastolic strain rate between the two groups. Transaminases and bilirubin correlated negatively with RV global longitudinal strain and RV-free wall strain in patients with end-stage liver cirrhosis. The Model for End-stage Liver Disease (MELD) score, predictor of 3-month mortality, correlated with parameters of RV structure and systolic function, and RA active function in patients with end-stage liver cirrhosis.
Conclusions:
RA and RV remodeling is present in patients with end-stage liver cirrhosis even though RV systolic function is preserved. Liver enzymes, bilirubin, and the MELD score correlated with RV and RA remodeling.
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