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Peripheral Biomarkers in Chronic Hepatitis D Infection: A Review
Zillah Cargill1, James Lok1,2, Geoffrey Dusheiko1
1Institute of Liver Studies, Kings College Hospital, London, UK.
Insights
Predicting outcomes in chronic hepatitis D (Hepatitis D Virus) is difficult. New peripheral biomarkers could help stratify patients, predict treatment response, and guide care for this severe liver disease.
Area of Science:
- Hepatology
- Virology
- Biomarker Discovery
Background:
- Chronic hepatitis D (HDV) is the most severe form of viral hepatitis.
- HDV infection is linked to higher rates of advanced liver disease, including cirrhosis and hepatocellular carcinoma, compared to hepatitis B monoinfection.
- HDV requires co-infection with hepatitis B virus (HBV) for replication.
Purpose of the Study:
- To review peripheral biomarkers for HDV infection.
- To explore the clinical utility of novel biomarkers for HBV activity in HDV patients.
- To identify areas for future biomarker development in managing HDV.
Main Methods:
- Literature review of peripheral biomarkers in HDV infection.
- Analysis of existing serological markers and novel HBV activity markers.
- Exploration of potential clinical applications for risk stratification and treatment monitoring.
Main Results:
- Accurate prediction of liver disease progression and treatment response in HDV remains a challenge with current biomarkers.
- Peripheral biomarkers offer potential for risk stratification and monitoring treatment response.
- Novel biomarkers of HBV activity are being investigated for their utility in HDV management.
Conclusions:
- Peripheral biomarkers are crucial for personalized care in chronic hepatitis D.
- Developing reliable biomarkers can aid in early identification of patients at high risk for advanced liver disease.
- Further validation in diverse populations and in the context of new therapies is essential for establishing biomarker roles.
Abstract:
Chronic hepatitis D represents the most severe form of viral hepatitis and is associated with higher rates of advanced fibrosis, cirrhosis and hepatocellular carcinoma than hepatitis B monoinfection. It is caused by the hepatitis D virus (HDV), a defective RNA virus that requires co-infection with hepatitis B (HBV) for hepatocyte entry and propagation. Accurate prediction of liver disease sequelae and treatment response using currently available serological biomarkers remains challenging. This article reviews peripheral biomarkers in HDV, including novel biomarkers of HBV activity, exploring their potential clinical utility and areas for future development. Peripheral biomarkers capable of risk stratifying patients with HDV, monitoring or predicting treatment response and elucidating the natural history of infection (including the complex relationship with HBV), would enable individualised care and early identification of those at greater risk of developing advanced liver disease. Establishing the role of these biomarkers in larger, ethnically diverse populations both on existing treatments and in the context of emerging antiviral therapies will be imperative going forward.
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