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Published on: May 25, 2020
Onset of heart failure determines the hepatic cell death pattern
Kerstin Herzer1, Guntje Kneiseler, Lars Peter Bechmann
1Department for Gastroenterology and Hepatology, University Hospital Essen, Hufelandstr, Germany.
Insights
Acute heart failure (AHF) causes more liver cell death than chronic heart failure (CHF). Higher M30 levels in AHF indicate worse prognosis, suggesting M30 as a survival marker for liver injury.
Area of Science:
- Hepatology
- Cardiology
- Biomarkers
Background:
- Heart failure (HF) can impact liver function, but mechanisms of liver damage are unclear.
- Hepatic cytokeratin-18 (CK18) epitopes M65 and M30 indicate overall and apoptotic cell death, respectively.
Purpose of the Study:
- To determine the predominant hepatic cell death pattern in acute versus chronic heart failure.
- To assess if CK18 assays predict disease progression in heart failure patients.
Main Methods:
- Prospective study of 21 acute HF (AHF) and 18 chronic HF (CHF) patients.
- Serum levels of CK18 M65 and M30 were measured.
Main Results:
- M65 and M30 levels were significantly higher in AHF compared to CHF.
- The M30/M65 ratio was significantly higher in CHF, indicating greater apoptotic cell death.
- Elevated M30 levels in AHF correlated with a worse prognosis.
Conclusions:
- The CK18 M30/M65 ratio may differentiate AHF from CHF-induced liver disease.
- M30 may serve as a prognostic marker for survival in AHF-induced liver injury.
Background And Rationale:
Acute and chronic heart failure (HF) may affect the liver, but the underlying mechanisms that lead to progressive liver damage are poorly understood. The hepatic cytokeratin-18 (CK18) epitopes M65 and M30 have been reported to distinguish between overall (necrotic) and apoptotic cell death, respectively. We aimed to evaluate the predominant hepatic cell death pattern in acute vs. chronic heart failure and examined if these assays predict the course of the disease.
Main Results:
In a prospective study comprising 21 patients with acute HF (AHF) and 18 patients with chronic HF (CHF) serum levels of M65 and M30 were assessed. Compared with CHF, M65 levels were significantly increased in patients with AHF (CHF: 1,283 ± 591.6U/l vs. AHF: 20,912 ± 15,132U/l, p < 0.001). In addition, M30 levels were significantly increased in AHF (CHF: 642.2 ± 177.4U/l vs. AHF: 3,844 ± 5,293U/l, p < 0.05), but the M30/M65 ratio was significantly higher in CHF (CHF: 0.54 ± 0.15 vs. AHF: 0.20 ± 0.19, p < 0.001), indicating a greater contribution of apoptotic cell death in CHF. AHF patients with higher M30 values had a worse prognosis.
Conclusions:
The ratio of CK18 M30/M65 is a potential marker to discriminate AHF from CHF induced LF and M30 might be a prognostic marker for survival in AHF induced liver injury.
Related Concept Videos
Pathophysiology of Heart Failure
Heart Failure I: Introduction
Heart Failure II: Pathophysiology
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Heart Failure IV: Classification and Diagnostic Evaluation
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

