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