Baseline hepatitis C virus resistance-associated substitutions present at frequencies lower than 15% may be clinically significant
| dc.contributor.author | Perales, Celia | |
| dc.contributor.author | Chen, Qian | |
| dc.contributor.author | Soria, Maria Eugenia | |
| dc.contributor.author | Gregori, Josep | |
| dc.contributor.author | Garcia Cehic, Damir | |
| dc.contributor.author | Nieto Aponte, Leonardo | |
| dc.contributor.author | Castells, Lluis | |
| dc.contributor.author | Imaz, Arkaitz | |
| dc.contributor.author | Llorens Revull, Meritxell | |
| dc.contributor.author | Domingo, Esteban | |
| dc.contributor.author | Buti, Maria | |
| dc.contributor.author | Esteban, Juan Ignacio | |
| dc.contributor.author | Rodríguez-Frías, Francisco | |
| dc.contributor.author | Quer, Josep | |
| dc.date.accessioned | 2020-12-09T19:08:18Z | |
| dc.date.available | 2020-12-09T19:08:18Z | |
| dc.date.issued | 2018-01-01 | |
| dc.date.updated | 2020-12-02T16:26:59Z | |
| dc.description.abstract | Background: 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.extent | 4 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.pmid | 30519058 | |
| dc.identifier.uri | https://hdl.handle.net/2445/172632 | |
| dc.language.iso | eng | |
| dc.publisher | Dove Medical Press Ltd. | |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.2147/IDR.S172226 | |
| dc.relation.ispartof | Infection and Drug Resistance, 2018, vol. 11, p. 2207-2210 | |
| dc.relation.uri | https://doi.org/10.2147/IDR.S172226 | |
| dc.rights | cc by-nc (c) Perales et al., 2018 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es/ | |
| dc.source | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | |
| dc.subject.classification | Hepatitis C | |
| dc.subject.classification | Medicaments antivírics | |
| dc.subject.other | Hepatitis C | |
| dc.subject.other | Antiviral agents | |
| dc.title | Baseline hepatitis C virus resistance-associated substitutions present at frequencies lower than 15% may be clinically significant | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion |
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