Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/172632
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dc.contributor.authorPerales, Celia-
dc.contributor.authorChen, Qian-
dc.contributor.authorSoria, Maria Eugenia-
dc.contributor.authorGregori, Josep-
dc.contributor.authorGarcia Cehic, Damir-
dc.contributor.authorNieto Aponte, Leonardo-
dc.contributor.authorCastells, Lluis-
dc.contributor.authorImaz, Arkaitz-
dc.contributor.authorLlorens Revull, Meritxell-
dc.contributor.authorDomingo, Esteban-
dc.contributor.authorButi, Maria-
dc.contributor.authorEsteban, Juan Ignacio-
dc.contributor.authorRodríguez-Frías, Francisco-
dc.contributor.authorQuer, Josep-
dc.date.accessioned2020-12-09T19:08:18Z-
dc.date.available2020-12-09T19:08:18Z-
dc.date.issued2018-01-01-
dc.identifier.urihttp://hdl.handle.net/2445/172632-
dc.description.abstractBackground: Controversy is ongoing about whether a minority mutant present at frequencies below 15% may be clinically relevant and should be considered to guide treatment. Methods: Resistance-associated substitution (RAS) studies were performed in patients before and at failure of antiviral treatments using Next-generation hepatitis C virus (HCV) sequencing (NGS). Results: We have found two patients with genotype 1a infection having RAS in 3.5%-7.1% of the viral population at baseline that were selected during ledipasvir + sofosbuvir treatment. Coselection of RAS located in a region not directly affected by the antiviral treatment also occurred. This observation calls into question, the recommendations to guide RAS-based direct-acting antiviral (DAA) treatment only when RAS are present in > 15% of the sequences generated. Conclusion: Our results suggests that RAS study should include all three HCV DAA target proteins and minority mutants should be considered as clinically relevant.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherDove Medical Press Ltd.-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2147/IDR.S172226-
dc.relation.ispartofInfection and Drug Resistance, 2018, vol. 11, p. 2207-2210-
dc.relation.urihttps://doi.org/10.2147/IDR.S172226-
dc.rightscc by-nc (c) Perales et al., 2018-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/-
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationHepatitis C-
dc.subject.classificationMedicaments antivírics-
dc.subject.otherHepatitis C-
dc.subject.otherAntiviral agents-
dc.titleBaseline hepatitis C virus resistance-associated substitutions present at frequencies lower than 15% may be clinically significant-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2020-12-02T16:26:59Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid30519058-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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