Acquired HIV drug resistance among adults living with HIV receiving first-line antiretroviral therapy in Rwanda: A cross-sectional nationally representative survey
Supporting Files
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6 2022 ; 6-2022
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Available in CDC Stacks on 2022-07-08T00:00:00Z
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Details
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Alternative Title:Antivir Ther
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Personal Author:Musengimana, Gentille
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Tuyishime, Elysee
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Kiromera, Athanase
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Malamba, Samuel S.
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Mulindabigwi, Augustin
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Habimana, Madjid R.
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Baribwira, Cyprien
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Ribakare, Muhayimpundu
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Habimana, Savio D.
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DeVos, Josh
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Mwesigwa, Richard C. N.
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Kayirangwa, Eugenie
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Semuhore, Jules M.
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Rwibasira, Gallican N.
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Suthar, Amitabh B.
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Remera, Eric
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Description:Background: ; We assessed the prevalence of acquired HIV drug resistance (HIVDR) and associated factors among patients receiving first-line antiretroviral therapy (ART) in Rwanda. ; Methods: ; This cross-sectional study included 702 patients receiving first-line ART for at least 6 months with last viral load (VL) results ≥1000 copies/mL. Blood plasma samples were subjected to VL testing; specimens with unsuppressed VL were genotyped to identify HIVDR-associated mutations. Data were analysed using STATA/SE. ; Results: ; Median time on ART was 86.4 months (interquartile range IQR, 44.8–130.2 months), and median CD4 count at ART initiation was 311 cells/mm3 (IQR, 197–484 cells/mm3). Of 414 (68.2%) samples with unsuppressed VL, 378 (88.3%) were genotyped. HIVDR included 347 (90.4%) non-nucleoside reverse transcriptase inhibitor- (NNRTI), 291 (75.5%) nucleoside reverse transcriptase inhibitor- (NRTI) and 13 (3.5%) protease inhibitor (PI) resistance-associated mutations. The most common HIVDR mutations were K65R (22.7%), M184V (15.4%) and D67N (9.8%) for NRTIs and K103N (34.4%) and Y181C/I/V/YC (7%) for NNRTIs. Independent predictors of acquired HIVDR included current ART regimen of zidovudine + lamivudine + nevirapine (adjusted odds ratio aOR, 3.333 95% confidence interval (CI): 1.022–10.870; p = 0.046) for NRTI resistance and current ART regimen of tenofovir + emtricitabine + nevirapine (aOR, 0.148 95% CI: 0.028–0.779; p = 0.025), zidovudine + lamivudine + efavirenz (aOR, 0.105 95% CI: 0.016–0.693; p = 0.020) and zidovudine + lamivudine + nevirapine (aOR, 0.259 95% CI: 0.084–0.793; p = 0.019) for NNRTI resistance. History of ever switching ART regimen was associated with NRTI resistance (aOR, 2.53 95% CI: 1.198–5.356; p = 0.016) and NNRTI resistance (aOR, 3.23 95% CI: 1.435–7.278, p = 0.005). ; Conclusion: ; The prevalence of acquired HIV drug resistance (HIVDR) was high among patient failing to re-suppress VL and was associated with current ART regimen and ever switching ART regimen. The findings of this study support the current WHO guidelines recommending that patients on an NNRTI-based regimen should be switched based on a single viral load test and suggests that national HIV VL monitoring of patients receiving ART has prevented long-term treatment failure that would result in the accumulation of TAMs and potential loss of efficacy of all NRTI used in second-line ART as the backbone in combination with either dolutegravir or boosted PIs.
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Source:Antivir Ther. 27(3):13596535221102690
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Pubmed ID:35593031
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Pubmed Central ID:PMC9263597
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Document Type:
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Funding:
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Volume:27
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Issue:3
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Main Document Checksum:urn:sha-512:cee978386b1ef12af045c73244d313ba36f2af8640c222ae126ac6f69f024622d47dde5a571f9c28d855507edf2db7f09d22fb3b1bfbadf53b57b70623837485
Supporting Files
File Language:
English
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