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dc.contributor.authorJohannessen, Asgeir
dc.contributor.authorNaman, Ezra
dc.contributor.authorKivuyo, Sokoine L
dc.contributor.authorKasubi, Mabula J
dc.contributor.authorHolberg-Petersen, Mona
dc.contributor.authorMatee, Mecky I
dc.contributor.authorGundersen, Svein G
dc.contributor.authorBruun, Johan N
dc.date.accessioned2015-10-09T02:13:31Z
dc.date.available2015-10-09T02:13:31Z
dc.date.issued2009
dc.identifier.citationBMC Infectious Diseases. 2009 Jul 07;9(1):108
dc.identifier.urihttp://hdl.handle.net/10852/46795
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 ≥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.
dc.language.isoeng
dc.rightsJohannessen et al; licensee BioMed Central Ltd.
dc.rightsAttribution 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/
dc.titleVirological efficacy and emergence of drug resistance in adults on antiretroviral treatment in rural Tanzania
dc.typeJournal article
dc.date.updated2015-10-09T02:13:31Z
dc.creator.authorJohannessen, Asgeir
dc.creator.authorNaman, Ezra
dc.creator.authorKivuyo, Sokoine L
dc.creator.authorKasubi, Mabula J
dc.creator.authorHolberg-Petersen, Mona
dc.creator.authorMatee, Mecky I
dc.creator.authorGundersen, Svein G
dc.creator.authorBruun, Johan N
dc.identifier.doihttp://dx.doi.org/10.1186/1471-2334-9-108
dc.identifier.urnURN:NBN:no-50975
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/46795/1/12879_2008_Article_873.pdf
dc.type.versionPublishedVersion
cristin.articleid108


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