Affiliation: | 1. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA;2. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine Inc., Bethesda, Maryland, USA;3. U.S. Army Medical Research Directorate–Africa, Kisumu, Kenya HJF Medical Research International, Kisumu, Kenya;4. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA U.S. Army Medical Research Directorate–Africa, Kericho, Kenya;5. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA HJF Medical Research International, Abuja, Nigeria;6. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA HJF Medical Research International, Mbeya, Tanzania;7. Makerere University-Walter Reed Project, Kampala, Uganda |
Abstract: | Objective We hypothesized that total body weight (TBW) gain after switching antiretroviral therapy (ART) regimen to tenofovir disoproxil fumarate/lamivudine/dolutegravir (TLD) may negatively impact ART adherence and viral load (VL) and therefore sought to examine these associations. Methods The ongoing African Cohort Study (AFRICOS) enrols people with HIV at 12 facilities in Kenya, Nigeria, Tanzania and Uganda supported by The US President's Emergency Plan for AIDS Relief. Among ART-experienced participants who switched to TLD, we used multivariable multinomial logistic regression to examine associations between pre−/post-TLD changes in percentage TBW (≥5% gain, <5% change, ≥5% loss) and changes in self-reported ART adherence (0, 1–2, ≥3 days missed doses in past 30 days) and VL [(<50 copies/mL (undetectable), 50–999 copies/mL (detectable, but suppressed), ≥1000 copies/mL (unsuppressed)]. Results Among 1508 participants, median time from starting TLD to follow-up was 9 months (interquartile range: 7–11). Overall, 438 (29.1%) participants experienced a TBW gain ≥5%, which was more common among females than among males (32.2% vs 25.2%, p = 0.005) and participants switching from efavirenz [32.0% vs nevirapine (19.9%) and boosted protease inhibitor (20.0%); p < 0.001]. Compared with a TBW change <5% [950 (63.0%) participants], TBW gain ≥5% was not significantly associated with more days with missed ART doses [adjusted odds ratio (aOR) = 0.77, 95% confidence interval (CI): 0.48–1.23] or VL becoming detectable and/or unsuppressed (aOR = 0.69, 95% CI: 0.41–1.16). Conclusions Although a substantial proportion of participants experienced weight gain after switching to TLD, we did not identify a significant impact on adherence or virological outcomes. |