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

被引:44
作者
Johannessen, Asgeir [1 ,2 ]
Naman, Ezra [2 ]
Kivuyo, Sokoine L. [3 ]
Kasubi, Mabula J. [4 ]
Holberg-Petersen, Mona [5 ]
Matee, Mecky I. [6 ]
Gundersen, Svein G. [7 ,8 ]
Bruun, Johan N. [1 ,9 ]
机构
[1] Oslo Univ Hosp, Ulleval Dept Infect Dis, Oslo, Norway
[2] Haydom Lutheran Hosp, HIV Care & Treatment Ctr, Mbulu, Tanzania
[3] Natl Inst Med Res, Haydom Res Stn, Mbulu, Tanzania
[4] Muhimbili Natl Hosp, Dept Microbiol & Immunol, Dar Es Salaam, Tanzania
[5] Oslo Univ Hosp, Ulleval Dept Microbiol, Oslo, Norway
[6] Muhimbili Univ Hlth & Allied Sci, Dept Microbiol & Immunol, Dar Es Salaam, Tanzania
[7] Sorlandet Hosp HF, Res Unit, Kristiansand, Norway
[8] Univ Agder, Ctr Dev Studies, Kristiansand, Norway
[9] Univ Hosp N Norway, Dept Infect Dis, Tromso, Norway
关键词
SUB-SAHARAN AFRICA; SOUTH-AFRICA; TREATMENT PROGRAM; TREATMENT FAILURE; THERAPY PROGRAMS; EARLY MORTALITY; HIGH PREVALENCE; SCALING-UP; OUTCOMES; REGIMEN;
D O I
10.1186/1471-2334-9-108
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
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 >= 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.
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