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dc.creatorRivero-Juárez, Antonioes
dc.creatorLópez Cortés, Luis Fernandoes
dc.creatorCamacho, Ángelaes
dc.creatorTorres Cornejo, Almudenaes
dc.creatorPineda Vergara, Juan Antonioes
dc.creatorMárquez-Solero, Manueles
dc.creatorRivero, Antonioes
dc.date.accessioned2021-07-02T14:46:18Z
dc.date.available2021-07-02T14:46:18Z
dc.date.issued2012-11-08
dc.identifier.citationRivero-Juárez, A., López Cortés, L.F., Camacho, Á., Torres Cornejo, A., Pineda Vergara, J.A., Márquez-Solero, M. y Rivero, A. (2012). Differences in HCV Viral Decline between Low and Standard-Dose Pegylated-Interferon-Alpha-2a with Ribavirin in HIV/HCV Genotype 3 Patients. PLoS ONE, 7 (11), art. n.48959.
dc.identifier.issn1932-6203 (electrónico)es
dc.identifier.urihttps://hdl.handle.net/11441/115068
dc.description.abstractBackground: The aim of the study was to analyze the different impact of standard and low-dose Peg-IFN-a2a/RBV therapies on HCV viral decline in HIV/HCV genotype 3 co-infected patients during the first weeks of treatment. Methods: Plasma HCV viral decline was analyzed between baseline and weeks 1, 2 and 4 in two groups of treatment-naı¨ve HCV genotype 3 patients with HIV co-infection. The Standard Dose Group (SDG) included patients who received Peg-IFN at 180 mg/per week with a weight-adjusted dose of ribavirin; Low-Dose Group (LDG) patients received Peg-IFN at 135 mg/per week with 800 mg/day ribavirin. The effect of IL28B genotype on HCV viral decline was evaluated in both groups. HCV viral decline was analyzed using a multivariate linear regression model. Results: One hundred and six patients were included: 48 patients in the SDG and 58 in the LDG. HCV viral decline for patients in the LDG was less than for those in the SDG (week 1:1.7260.74 log10 IU/mL versus 1.7860.67 log10 IU/mL, p = 0.827; week 2:2.360.89 log10 IU/mL versus 3.0161.02 log10 IU/mL, p = 0.013; week 4:3.5261.2 log10 IU/mL versus 4.0961.1 log10 IU/mL, p = 0.005). The linear regression model identified the Peg-IFN/RBV dose as an independent factor for HCV viral decline at week 4. Conclusions: Our results showed that HCV viral decline was less for patients in the low-dose group compared to those receiving the standard dose. Until a randomized clinical trial is conducted, clinicians should be cautious about using lower doses of Peg-IFN/RBV in HIV/HCV genotype 3 co-infected patients.es
dc.description.sponsorshipFundación Progreso y Salud, Consejería de Salud de la Junta de Andalucía (refs. 0036/2010, PI-0247-2010 and PI-0208 and 0124/2008es
dc.description.sponsorshipSpanish Health Ministry (ISCIII-RETIC RD06/006, and projects PI10/0164 and PI10/01232)es
dc.description.sponsorshipFundación Progreso y Salud, Consejería de Salud de la Junta de Andalucía (Reference AI0011-2010)es
dc.description.sponsorshipInstituto de Salud Carlos III (grant number Programa-I3SNS)es
dc.formatapplication/pdfes
dc.format.extent6 p.es
dc.language.isoenges
dc.publisherPublic Library of Sciencees
dc.relation.ispartofPLoS ONE, 7 (11), art. n.48959.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectLow-Dose Groupes
dc.subjectHCV Virales
dc.subjectStandard Dose Groupes
dc.subjectPeg-IFN/RBV treatmentes
dc.titleDifferences in HCV Viral Decline between Low and Standard-Dose Pegylated-Interferon-Alpha-2a with Ribavirin in HIV/HCV Genotype 3 Patientses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.projectID0036/2010es
dc.relation.projectIDPI-0247-2010es
dc.relation.projectIDPI-0208es
dc.relation.projectID0124/2008es
dc.relation.projectIDISCIII-RETIC RD06/006es
dc.relation.projectIDPI10/0164es
dc.relation.projectIDPI10/01232es
dc.relation.projectIDReference AI0011-2010es
dc.relation.projectIDPrograma-I3SNSes
dc.relation.publisherversionhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0048959es
dc.identifier.doi10.1371/journal.pone.0048959es
dc.journaltitlePLoS ONEes
dc.publication.volumen7es
dc.publication.issue11es
dc.publication.initialPageart. n.48959es

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