Serum NT-ProBNP potential marker of cirrhotic cardiomyopathy
Maya Risteska1, Ludmila Vladimirova-Kitova2, Vladimir Andonov2
1St George University Hospital, Plovdiv, Bulgaria.
Insights
Cirrhotic cardiomyopathy, a cardiac dysfunction in liver cirrhosis, presents with impaired contractility and electrical abnormalities. Elevated brain natriuretic peptide (BNP) and N-terminal pro B-type natriuretic peptide (NT-proBNP) levels indicate cardiac issues in these patients.
Area of Science:
- Cardiology
- Hepatology
- Biochemistry
Background:
- Liver cirrhosis is frequently linked to cardiac dysfunction.
- Cirrhotic cardiomyopathy is characterized by systolic and diastolic dysfunction, electrical abnormalities, and chronotropic incompetence.
- Elevated levels of brain natriuretic peptide (BNP) and N-terminal pro B-type natriuretic peptide (NT-proBNP) are observed in cirrhosis patients with cardiac dysfunction.
Purpose of the Study:
- To investigate the relationship between liver cirrhosis and cardiac dysfunction.
- To explore the clinical features of cirrhotic cardiomyopathy.
- To examine the role of BNP and NT-proBNP as biomarkers in cirrhotic cardiomyopathy.
Main Methods:
- Review of previous studies on liver cirrhosis and cardiac function.
- Analysis of clinical features associated with cirrhotic cardiomyopathy.
- Assessment of BNP and NT-proBNP levels in cirrhosis patients.
Main Results:
- Cardiac dysfunction is a common complication of liver cirrhosis.
- Key features include impaired contractility, diastolic dysfunction, and electrical abnormalities.
- Elevated BNP and NT-proBNP levels correlate with both systolic and diastolic dysfunction.
Conclusions:
- Cirrhotic cardiomyopathy is a significant clinical entity in liver cirrhosis.
- BNP and NT-proBNP serve as important indicators of cardiac dysfunction in these patients.
Introduction:
Based on many previous studies, liver cirrhosis is traditionally associated with cardiac dysfunction. The main clinical features of cirrhotic cardiomyopathy include attenuated systolic contractility in response to physiologic or pharmacologic strain, diastolic dysfunction, electrical conductance abnormalities, and chronotropic incompetence. Previous studies have found that the levels of brain natriuretic peptide (BNP) and its precursor the N-terminal pro B-type natriuretic peptide (NT-proBNP) are elevated in cirrhosis with systolic as well as diastolic dysfunction.
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