Virological efficacy and emergence of drug resistance in adults on antiretroviral treatment in rural Tanzania

Show simple item record

dc.contributor.author Johannessen, A.
dc.contributor.author Naman, E.
dc.contributor.author Kivuyo, S.L.
dc.contributor.author Kasubi, M.J.
dc.contributor.author Petersen, M.H.
dc.contributor.author Matee, M.I.
dc.contributor.author Gundersen, S.G.
dc.contributor.author Bruun, J.N.
dc.date.accessioned 2013-02-12T13:33:59Z
dc.date.available 2013-02-12T13:33:59Z
dc.date.issued 2009
dc.identifier.issn 1471-2334-9-108
dc.identifier.other doi:10.1186/1471-2334-9-108
dc.identifier.uri http://hdl.handle.net/123456789/361
dc.description.abstract Background: 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 ³1 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 crossresistance 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_GB
dc.language.iso en en_GB
dc.publisher BioMed Central en_GB
dc.relation.ispartofseries BMC Infectious Diseases; 9:108
dc.subject Virological efficacy en_GB
dc.subject Drug resistance en_GB
dc.subject Antiretroviral en_GB
dc.subject Tanzania en_GB
dc.title Virological efficacy and emergence of drug resistance in adults on antiretroviral treatment in rural Tanzania en_GB
dc.type Article en_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search MUHAS IR


Advanced Search

Browse

My Account