| Literature DB >> 21596633 |
Véronique Loustaud-Ratti1, Paul Carrier, Annick Rousseau, Marianne Maynard, Gérard Babany, Sophie Alain, Christian Trépo, Victor De Ledinghen, Marc Bourlière, Stanislas Pol, Vincent Di Martino, Jean-Pierre Zarski, Alexandrina Pinta, Denis Sautereau, Pierre Marquet.
Abstract
Ribavirin remains today a pivotal drug in the treatment of hepatitis C; in standard double therapy, as well as in triple combination with direct antiviral agents, ribavirin reduces relapse and can double the sustained virological response obtained with peginterferon alone or in association with direct antiviral agents. In the complex network of interacting factors determining sustained virological response independently of known predictive factors related to host and virus, two modern tools are emerging: polymorphisms in the IL28B gene and very early exposure to ribavirin. The use of a pharmacokinetic-pharmacodynamic model of early ribavirin exposure to adjust the dose individually would help promote a safer ribavirin use and improve sustained virological response. The variability of the influence of ribavirin exposure on anaemia is probably genetically determined; however, the low prevalence of the implicated protective alleles of the inosine triphosphate pyrophosphatase gene could explain their lack of influence on sustained virological response.Entities:
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Year: 2011 PMID: 21596633 DOI: 10.1016/j.dld.2011.04.002
Source DB: PubMed Journal: Dig Liver Dis ISSN: 1590-8658 Impact factor: 4.088