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Published on: September 30, 2021
[Genetics and hepatitis C treatment: towards a personalized treatment?]
Sabela Lens García1, Mairene Coto-Llerena, Sofía Pérez del Pulgar Gallart
1Servicio de Hepatología, Institut de Malalties Digestives i Metabòliques, Hospital Clínic, Barcelona, España.
Insights
Genetic variations near the IL28B gene significantly predict treatment success for chronic hepatitis C virus (HCV) infection. Understanding these host genetics improves patient management and treatment strategies for liver disease.
Area of Science:
- Hepatology
- Virology
- Genetics
Background:
- Chronic hepatitis C virus (HCV) infection leads to liver cirrhosis and cancer, a major cause of liver transplantation.
- Current treatments (pegylated interferon and ribavirin) have limited efficacy, with only 50% achieving sustained virological response.
- Host and viral factors influence treatment outcomes in chronic hepatitis C.
Purpose of the Study:
- To review recent genetic studies on hepatitis C treatment response.
- To discuss the clinical implications of host genetic variations, particularly IL28B polymorphisms.
- To highlight the growing role of genetics in managing liver diseases.
Main Methods:
- Review of recent genetic studies focusing on IL28B gene polymorphisms.
- Analysis of the predictive value of these polymorphisms for HCV clearance and treatment response.
- Synthesis of clinical implications for liver disease management.
Main Results:
- Polymorphisms near the IL28B gene are strong predictors of spontaneous HCV clearance.
- IL28B gene variations significantly influence response rates to antiviral treatment in chronic hepatitis C.
- Genetics is emerging as a crucial factor in personalized hepatitis C management.
Conclusions:
- IL28B genotyping can help predict treatment outcomes in chronic hepatitis C.
- Incorporating genetic information into clinical practice can optimize treatment strategies.
- Genetics plays an increasingly vital role in the management of liver diseases like hepatitis C.
Abstract:
Chronic HCV (hepatitis C virus) infection is an important cause of liver cirrhosis and hepatocellular carcinoma worldwide. HCV-related cirrhosis is the main indication for liver transplantation in our geographical area. Thus, treatment of this disease represents an important economical burden for the Health Care System. Current treatment of hepatitis C consists of pegylated interferon and ribavirin: only half of the patients achieve a sustained virological response after treatment. Factors related to the virus and the host influence response to treatment. Polymorphisms near the gene IL28B (encoding interferon-λ-3) have been recently identified as strong predictors of spontaneous HCV clearance in acute infection and of response to antiviral treatment in chronic hepatitis C. The aim of this article is to review the genetic studies that have emerged during the last months and its clinical implications, as well as to emphasize how Genetics is gaining importance in the management of liver diseases.
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