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Clinical long-term outcome of hepatitis D compared to hepatitis B monoinfection
Anika Wranke1, Benjamin Heidrich1, Katja Deterding1
1Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
Insights
Hepatitis D virus (HDV) infection accelerates cirrhosis progression more than Hepatitis B virus (HBV) monoinfection. However, once cirrhosis is established, it becomes the primary risk factor for liver complications, regardless of HDV presence.
Area of Science:
- Hepatology
- Virology
- Clinical Medicine
Background:
- Hepatitis D virus (HDV) causes severe chronic viral hepatitis.
- The role of underlying cirrhosis in disease progression remains unclear.
- Comparing long-term outcomes of HDV vs. HBV infection is crucial.
Purpose of the Study:
- To compare the long-term outcomes of HDV infection versus HBV monoinfection.
- To evaluate the impact of cirrhosis on disease progression in both infections.
- To identify risk factors for liver-related end points.
Main Methods:
- Retrospective study of 175 patients with chronic hepatitis D (CHD).
- Matched cohort of 175 patients with chronic hepatitis B (CHB) monoinfection.
- Defined liver-related end points including hepatic decompensation, transplantation, HCC, and death.
Main Results:
- Clinical complications occurred earlier and more frequently in CHD patients.
- HDV infection was independently associated with a higher risk of end points (HR: 3.0).
- In cirrhotic patients, no significant difference in end points between HBV and HDV; CHB patients had higher HCC rates.
Conclusions:
- HDV accelerates cirrhosis progression compared to HBV.
- Established cirrhosis, not HDV itself, is the dominant risk factor for liver complications and HCC.
- Cirrhosis is the key determinant of poor outcomes in chronic viral hepatitis.
Background And Aims:
Hepatitis D virus (HDV) infection causes the most severe form of chronic viral hepatitis. However, it is still unclear to what extent the underlying cirrhosis may contribute to disease progression. The aim of this study was to compare the long-term outcome of HDV infection with HBV monoinfection in a single-center cohort of both non-cirrhotic and cirrhotic patients.
Method:
We retrospectively studied 175 patients with chronic hepatitis D (CHD) who were followed for at least 6 months (median of 6.3 (0.6-23.6) years). In addition, we selected 175 patients with HBV monoinfection (CHB) who were matched for gender, age, region of origin, HBeAg status, and bilirubin. Liver-related clinical end points were defined as hepatic decompensation (ascites, encephalopathy, variceal bleeding), liver transplantation, HCC, or liver-related death.
Results:
Clinical complications developed earlier (4.6 vs. 6.2 years) and more frequently (35.4% vs. 12.6%, p < 0.01) in CHD patients. In a multivariate Cox regression, HDV infection was independently associated with the development of end points (p < 0.01; HR: 3.0; 95% CI 1.4-6.4). However, in cirrhotic patients there were no significant differences between HBV and HDV in the development of end points. Besides, CHB patients with cirrhosis developed more frequently HCC (35.5%) than CHD patients with cirrhosis (18.5%).
Conclusion:
Our results confirmed that HDV leads to a faster progression to cirrhosis compared to HBV. However, once cirrhosis is present, not HDV but the underlying cirrhosis is the dominate intrinsic risk factor for the development of liver-related end points and for the progression to HCC.
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