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Impact of Steatosis on HCV Progression and Treatment Outcomes

By Liz Highleyman

Liver steatosis (fat accumulation in liver cells) is common among patients with chronic hepatitis C virus (HCV) infection, especially those with genotype 3 virus. Past research indicates that steatosis is associated with accelerated liver fibrosis progression and poorer response to antiviral therapy.

As described in the January 2007 Journal of Viral Hepatitis, an international team of researchers monitored steatosis in liver biopsy samples from 231 patients with chronic HCV infection who were treated with pegylated interferon-alpha plus ribavirin in the Phase III DITTO trial. The degree of steatosis, along with relevant metabolic parameters, was correlated with early HCV clearance and final outcomes of treatment.

The researchers wrote that, "Our data suggest that the presence of steatosis impairs the early reduction of viral load during treatment in patients infected with HCV genotype 3 and non-3."

They added that, "Steatosis negatively affected the final outcome of treatment mainly in patients infected with HCV genotype non-3 virus."

Based on these findings, the investigators proposed that, "interventions aiming at reducing hepatic steatosis prior to the onset of antiviral therapy may be of benefit to patients infected with HCV of the non-3 genotypes. Patients infected with genotype 3, on the other hand, should be offered early antiviral treatment."

Sahlgrenska University Hospital, Göteborg, Sweden; Royal Free Hospital, London, UK; Hôpital Henri Mondor, Université Paris XII, Créteil, France; Saarland University Hospital, Homburg/Saar, Germany; University Hospital Rotterdam Dijkzigt, Rotterdam, the Netherlands; University of Geneva, Switzerland; Azienda Ospedaliera di Parma, Italy; Bar-Ilan University, Ramat-Gan, Israel.

1/23/07

Reference
J Westin, M Lagging, A P Dhillon, and others. Impact of hepatic steatosis on viral kinetics and treatment outcome during antiviral treatment of chronic HCV infection. Journal of Viral Hepatitis 14(1): 29-35. January 2007.



 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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