<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Martin MA</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Data on the population-scale impact of dolutegravir (DTG)-based HIV regimens in sub-Saharan Africa are extremely limited. We used data from a surveillance cohort in southern Uganda to assess viral suppression and antiretroviral (ART) resistance over 10-years alongside DTG scale-up.&lt;h4>Methods&lt;/h4>Consenting participants in the population-based Rakai Community Cohort Study between August 2011 and March 2023 aged 15-59 completed questionnaires and provided samples for HIV testing, viral load quantification, and viral deep-sequencing. We collected data on DTG-utilization at HIV care clinics. We estimated the prevalence of HIV suppression (&lt;1,000 copies/mL) and ART resistance using robust Poisson regression. Bayesian logistic regression quantified associations between resistance and individual-level suppression across surveys.&lt;h4>Findings&lt;/h4>Among 20,383 people living with HIV (PLHIV), suppression increased from 57.1% (95% confidence interval [CI]: 55.4%-58.8%) to 90.3% (95%CI: 89.2%-91.4%) between 2014 and 2022. By 2020 84.4% (95%CI: 83.7%-85.2%) and 64.6% (95%CI: 63.9%-65.3%) of men and women were on DTG regimens. Among treatment-experienced viremic PLHIV, overall resistance decreased from 51.1% (95%CI: 40.7%-64.1%, 2014) to 27.9% (95%CI: 21.3%-36.5%, 2022). Only two participants harbored intermediate/high-level DTG resistance, attributable to inQ148R, inE138K, and inG140A. Low-level INSTI resistance (inS153Y) was observed in 23/207 (7.5%) of viremic individuals, with putative evidence of transmission. By 2022, suppression was unrelated to prior history of NNRTI/NRTI resistance (risk ratios: 1.14, 95%HPD: 0.96-1.32 and 1.12, 95%HPD: 0.88 - 1.35).&lt;h4>Interpretation&lt;/h4>Viral suppression increased during the DTG-transition with minimal emerging intermediate/high-level resistance. Falling resistance among treatment-experienced PLHIV underscores the role of ART adherence in reducing viremia. The emergence of inS153Y justifies continued genomic surveillance of ART resistance.&lt;h4>Funding&lt;/h4>National Institutes of Health and the Gates Foundation.</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2025.09.01.25334862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12424902</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Patterns of HIV-1 viral load suppression and drug resistance during the dolutegravir transition: a population-based longitudinal study.</pubmed_title><pmcid>PMC12424902</pmcid><pubmed_authors>Kigozi G</pubmed_authors><pubmed_authors>Martin MA</pubmed_authors><pubmed_authors>MacIntyre-Cockett G</pubmed_authors><pubmed_authors>Kennedy CE</pubmed_authors><pubmed_authors>Bonsall D</pubmed_authors><pubmed_authors>Reynolds SJ</pubmed_authors><pubmed_authors>Blenkinsop A</pubmed_authors><pubmed_authors>Tobian AAR</pubmed_authors><pubmed_authors>Fraser C</pubmed_authors><pubmed_authors>Laeyendecker O</pubmed_authors><pubmed_authors>Quinn TC</pubmed_authors><pubmed_authors>Grayson NE</pubmed_authors><pubmed_authors>Gupta RK</pubmed_authors><pubmed_authors>Moyo S</pubmed_authors><pubmed_authors>Nalugoda F</pubmed_authors><pubmed_authors>Ratmann O</pubmed_authors><pubmed_authors>Galiwango RM</pubmed_authors><pubmed_authors>Ssekubugu R</pubmed_authors><pubmed_authors>Abeler-Dorner L</pubmed_authors><pubmed_authors>Moffa M</pubmed_authors><pubmed_authors>Nakigozi G</pubmed_authors><pubmed_authors>Grabowski MK</pubmed_authors><pubmed_authors>Kagaayi J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Patterns of HIV-1 viral load suppression and drug resistance during the dolutegravir transition: a population-based longitudinal study.</name><description>&lt;h4>Background&lt;/h4>Data on the population-scale impact of dolutegravir (DTG)-based HIV regimens in sub-Saharan Africa are extremely limited. We used data from a surveillance cohort in southern Uganda to assess viral suppression and antiretroviral (ART) resistance over 10-years alongside DTG scale-up.&lt;h4>Methods&lt;/h4>Consenting participants in the population-based Rakai Community Cohort Study between August 2011 and March 2023 aged 15-59 completed questionnaires and provided samples for HIV testing, viral load quantification, and viral deep-sequencing. We collected data on DTG-utilization at HIV care clinics. We estimated the prevalence of HIV suppression (&lt;1,000 copies/mL) and ART resistance using robust Poisson regression. Bayesian logistic regression quantified associations between resistance and individual-level suppression across surveys.&lt;h4>Findings&lt;/h4>Among 20,383 people living with HIV (PLHIV), suppression increased from 57.1% (95% confidence interval [CI]: 55.4%-58.8%) to 90.3% (95%CI: 89.2%-91.4%) between 2014 and 2022. By 2020 84.4% (95%CI: 83.7%-85.2%) and 64.6% (95%CI: 63.9%-65.3%) of men and women were on DTG regimens. Among treatment-experienced viremic PLHIV, overall resistance decreased from 51.1% (95%CI: 40.7%-64.1%, 2014) to 27.9% (95%CI: 21.3%-36.5%, 2022). Only two participants harbored intermediate/high-level DTG resistance, attributable to inQ148R, inE138K, and inG140A. Low-level INSTI resistance (inS153Y) was observed in 23/207 (7.5%) of viremic individuals, with putative evidence of transmission. By 2022, suppression was unrelated to prior history of NNRTI/NRTI resistance (risk ratios: 1.14, 95%HPD: 0.96-1.32 and 1.12, 95%HPD: 0.88 - 1.35).&lt;h4>Interpretation&lt;/h4>Viral suppression increased during the DTG-transition with minimal emerging intermediate/high-level resistance. Falling resistance among treatment-experienced PLHIV underscores the role of ART adherence in reducing viremia. The emergence of inS153Y justifies continued genomic surveillance of ART resistance.&lt;h4>Funding&lt;/h4>National Institutes of Health and the Gates Foundation.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-26T20:10:50.072Z</modification><creation>2026-05-26T03:06:31.411Z</creation></dates><accession>S-EPMC12424902</accession><cross_references><pubmed>40950453</pubmed><doi>10.1101/2025.09.01.25334862</doi></cross_references></HashMap>