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dc.contributor.authorJohannessen, Asgeir
dc.contributor.authorNaman, Ezra
dc.contributor.authorKivujo, Sokoine
dc.contributor.authorKasubi, Mabula
dc.contributor.authorHolberg-Petersen, Mona
dc.contributor.authorMatee, Mecky
dc.contributor.authorGundersen, Svein Gunnar
dc.contributor.authorBruun, Johan
dc.date.accessioned2010-03-26T13:00:36Z
dc.date.issued2009
dc.identifier.citationJohannessen, A., Naman, E., Kivuyo, S., Kasubi, M., Holberg-Petersen, M., Matee, M., et al. (2009). Virological efficacy and emergence of drug resistance in adults on antiretroviral treatment in rural Tanzania. Bmc Infectious Diseases, 9(1), 108. doi: 10.1186/1471-2334-9-108en
dc.identifier.issn1471-2334
dc.identifier.urihttp://hdl.handle.net/11250/135294
dc.descriptionArticle published in the journal: Bmc Infectious Diseases Also available from: http://dx.doi.org/10.1186/1471-2334-9-108en
dc.description.abstractBACKGROUND:Virological response to antiretroviral treatment (ART) in rural Africa is poorly described. We examined virological efficacy and emergence of drug resistance in adults receiving first-line ART for up to 4 years in rural Tanzania.METHODS:Haydom Lutheran Hospital has provided ART to HIV-infected patients since October 2003. A combination of stavudine or zidovudine with lamivudine and either nevirapine or efavirenz is the standard first-line regimen. Nested in a longitudinal cohort study of patients consecutively starting ART, we carried out a cross-sectional virological efficacy survey between November 2007 and June 2008. HIV viral load was measured in all adults who had completed at least 6 months first-line ART, and genotypic resistance was determined in patients with viral load >1000 copies/mL.RESULTS:Virological response was measured in 212 patients, of whom 158 (74.5%) were women, and median age was 35 years (interquartile range [IQR] 29-43). Median follow-up time was 22.3 months (IQR 14.0-29.9). Virological suppression, defined as <400 copies/mL, was observed in 187 patients (88.2%). Overall, prevalence of [greater than or equal to]1 clinically significant resistance mutation was 3.9, 8.4, 16.7 and 12.5% in patients receiving ART for 1, 2, 3 and 4 years, respectively. Among those successfully genotyped, the most frequent mutations were M184I/V (64%), conferring resistance to lamivudine, and K103N (27%), Y181C (27%) and G190A (27%), conferring resistance to non-nucleoside reverse transcriptase inhibitors (NNRTIs), whereas 23% had thymidine analogue mutations (TAMs), associated with cross-resistance to all nucleoside reverse transcriptase inhibitors (NRTIs). Dual-class resistance, i.e. resistance to both NRTIs and NNRTIs, was found in 64%.CONCLUSION:Virological suppression rates were good up to 4 years after initiating ART in a rural Tanzanian hospital. However, drug resistance increased with time, and dual-class resistance was common, raising concerns about exhaustion of future antiretroviral drug options. This study might provide a useful forecast of drug resistance and demand for second-line antiretroviral drugs in rural Africa in the coming years.en
dc.format.extent248904 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoengen
dc.publisherBMC Publishingen
dc.titleVirological efficacy and emergence of drug resistance in adults on antiretroviral treatment in rural Tanzaniaen
dc.typeJournal articleen
dc.subject.nsiVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Communicable diseases: 776en
dc.source.pagenumber108en
dc.source.volume9en
dc.source.journalBmc Infectious Diseasesen
dc.source.issue1en


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