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dc.contributor.authorWoottichai Khamduangen_US
dc.contributor.authorCatherine Gaudy-Graffinen_US
dc.contributor.authorNicole Ngo-Giang-Huongen_US
dc.contributor.authorGonzague Jourdainen_US
dc.contributor.authorAlain Moreauen_US
dc.contributor.authorNuananong Luekamlungen_US
dc.contributor.authorGuttiga Halueen_US
dc.contributor.authorYuwadee Buranawanitchakornen_US
dc.contributor.authorSura Kunkongkapanen_US
dc.contributor.authorSudanee Buranabanjasateanen_US
dc.contributor.authorMarc Lallemanten_US
dc.contributor.authorWasna Sirirungsien_US
dc.contributor.authorAlain Goudeauen_US
dc.date.accessioned2018-09-04T05:59:37Z-
dc.date.available2018-09-04T05:59:37Z-
dc.date.issued2012-07-31en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-84864447642en_US
dc.identifier.other10.1371/journal.pone.0042184en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84864447642&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51266-
dc.description.abstractBackground: Approximately 4 million of people are co-infected with HIV and Hepatitis B virus (HBV). In resource-limited settings, the majority of HIV-infected patients initiate first-line highly active antiretroviral therapy containing lamivudine (3TC-containing-HAART) and long-term virological response of HBV to lamivudine-containing HAART in co-infected patients is not well known. Methodology/Principal Finding: HIV-HBV co-infected patients enrolled in the PHPT cohort (ClinicalTrials.gov NCT00433030) and initiating a 3TC-containing-HAART regimen were included. HBV-DNA, HIV-RNA, CD4+ T-cell counts and alanine transaminase were measured at baseline, 3 months, 12 months and then every 6 months up to 5 years. Kaplan-Meier analysis was used to estimate the cumulative rates of patients who achieved and maintained HBV-DNA suppression. Of 30 co-infected patients, 19 were positive for HBe antigen (HBeAg). At initiation of 3TC-containing-HAART, median HBV DNA and HIV RNA levels were 7.35 log10 IU/mL and 4.47 log10 copies/mL, respectively. At 12 months, 67% of patients achieved HBV DNA suppression: 100% of HBeAg-negative patients and 47% of HBeAg-positive. Seventy-three percent of patients had HIV RNA below 50 copies/mL. The cumulative rates of maintained HBV-DNA suppression among the 23 patients who achieved HBV-DNA suppression were 91%, 87%, and 80% at 1, 2, and 4 years respectively. Of 17 patients who maintained HBV-DNA suppression while still on 3TC, 4 (24%) lost HBsAg and 7 of 8 (88%) HBeAg-positive patients lost HBeAg at their last visit (median duration, 59 months). HBV breakthrough was observed only in HBeAg-positive patients and 6 of 7 patients presenting HBV breakthrough had the rtM204I/V mutations associated with 3TC resistance along with rtL180M and/or rtV173L. Conclusions: All HBeAg-negative patients and 63% of HBeAg-positive HIV-HBV co-infected patients achieved long-term HBV DNA suppression while on 3TC-containing-HAART. This study provides information useful for the management of co-infected patients in resource-limited countries where the vast majority of co-infected patients are currently receiving 3TC. © 2012 Khamduang et al.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleLong-term hepatitis B virus (HBV) response to Lamivudine-containing highly active antiretroviral therapy in HIV-HBV co-infected patients in Thailanden_US
dc.typeJournalen_US
article.title.sourcetitlePLoS ONEen_US
article.volume7en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversite Francois Rabelais Faculte de Medicineen_US
article.stream.affiliationsInstitute of research for development, Thailanden_US
article.stream.affiliationsHarvard School of Public Healthen_US
article.stream.affiliationsLamphun Hospitalen_US
article.stream.affiliationsPhayao Hospitalen_US
article.stream.affiliationsChiang Kham Hospitalen_US
article.stream.affiliationsMae Sai Hospitalen_US
article.stream.affiliationsMae Chan Hospitalen_US
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