Resistance to Antiretroviral Drugs in Treated and Drug-Naive Patients in the Democratic Republic of Congo

被引:27
|
作者
Muwonga, Jeremie [2 ,3 ]
Edidi, Samuel [2 ]
Butel, Christelle [5 ]
Vidal, Nicole [5 ]
Monleau, Marjorie [5 ]
Okenge, Augustin [4 ]
Mandjo, Jean Lambert [4 ]
Mukumbi, Henry [6 ,8 ]
Muyembe, Jean Jacques [3 ]
Mbayo, Ferdinand [3 ]
Nzongola, Donatien Kayembe [3 ]
Delaporte, Eric [5 ]
Boillot, Francois [7 ]
Peeters, Martine [1 ,5 ]
机构
[1] IRD, Lab Retrovirus, UMI 233, F-34394 Montpellier 1, France
[2] Gen Hosp Kinshasa, AIDS Natl Reference Lab LNRS, Kinshasa, DEM REP CONGO
[3] Univ Kinshasa, Dept Med Biol, Kinshasa, DEM REP CONGO
[4] AIDS Natl Control Program PNLS, Kinshasa, DEM REP CONGO
[5] Univ Montpellier I, Montpellier, France
[6] AMO Congo, Congo, DEM REP CONGO
[7] Alter Sante Int & Dev, Montpellier, France
[8] Int Union TB & Lung Dis, Paris, France
关键词
HIV; drug resistance; Africa; Democratic Republic of Congo; PUBLIC-HEALTH APPROACH; TYPE-1; GROUP-M; ADULT PATIENTS; SCALING-UP; FOLLOW-UP; HIV; MUTATIONS; THERAPY; DIVERSITY; PROGRAMS;
D O I
10.1097/QAI.0b013e31821f596c
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: We studied virological outcome and drug resistance in patients on antiretroviral therapy (ART) in health care centers in the Democratic Republic of Congo and looked for the presence of drug resistance in antiretroviral-naive patients attending the same clinics. Methods: In 2008, we conducted a cross-sectional survey among patients on ART for >= 12 months in 4 major cities [Kinshasa (n = 289), Matadi (n = 198), Lubumbashi (n = 77), and Mbuji-Mayi (n = 103)]. Genotypic drug resistance tests were done with an in-house assay on samples with viral load > 1000 copies/mL. ART-naive patients (n = 283) were also consecutively enrolled in the same clinics. Results: Of the 667 patients on ART, > 98% received Lamivudine + Stavudine/azidothymidine + Nevirapine/Efavirenz as first-line regimen and 74.4% were women. Median time on ART was 25 months [interquartile ratio (IQR), 19-32] in Kinshasa, 26 months (IQR, 19-32) in Matadi, 27 months (IQR, 19-44) in Lubumbashi, and 19 months (IQR, 16-24) in Mbuji-Mayi. A total of 97 patients (14.6%) had viral load > 1000 copies/mL, and among the 93 successfully sequenced samples, 78 (83.9%) were resistant to at least 1 drug of their ART regimen: 68 harbored resistance mutations to nucleoside reverse transcriptase inhibitor (NRTI) and nonnucleoside reverse transcriptase inhibitor (NNRTI), 2 to NRTI only, 7 to NNRTI only, and 1 to NRTI + NNRTI + protease inhibitor. The majority of patients, 70/78 (89.7%), were resistant to at least 2 of the 3 drugs from their treatment. The use of next-generation NNRTI, etravirine was already compromised for 19.2% (15/78) of the patients and 7 patients had the K65R mutation compromising the use of tenofovir in second-line regimens. The proportion of antiretroviral-resistant patients increased over time from 8.4% to 18.6% for patients on ART for 12-23 months or > 35 months (P = 0.013), respectively. Virological failure and rates of drug resistance were significantly higher among men than women, 19.9% versus 8.8%, respectively (P = 0.0001). Among the 253 recently diagnosed patients, 20 (7.9%) harbored resistance mutations. Conclusions: The accumulation of drug resistance mutations with time on ART needs further attention, and surveillance should be reinforced in ART programs in sub-Saharan Africa.
引用
收藏
页码:S27 / S33
页数:7
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