Temporal dynamics and drivers of durable HIV viral load suppression and persistent high- and low-level viremia during Universal Test and Treat scale-up in Uganda: a population-based study

Introduction: Population-level data on durable HIV viral load suppression (VLS) following implementation of Universal Test and Treat (UTT) in Africa are limited. We assessed trends in durable VLS and viremia among persons living with HIV in 40 Ugandan communities during UTT scale-up. Methods: In 2015-2020, we measured VLS (defined as <200 RNA copies/mL) among participants in the Rakai Community Cohort Study, a longitudinal population-based HIV surveillance cohort in southern Uganda. Persons with unsuppressed viral loads were characterized as having low-level (200-999 copies/mL) or high-level (>1,000 copies/mL) viremia. Individual virologic outcomes were assessed over two consecutive RCCS survey visits (i.e., visit-pairs; ~18 month visit intervals) and classified as durable VLS (<200 copies/mL at both visits), new/renewed VLS (<200 copies/mL at follow-up only), viral rebound (<200 copies/mL at initial visit only), or persistent viremia (<200 copies/mL at neither visit). Population prevalence of each outcome was assessed over calendar time. Community-level prevalence and individual-level predictors of persistent high-level viremia were also assessed using multivariable Poisson regression with generalized estimating equations. Results: Overall, 3,080 participants contributed 4,604 visit-pairs over three survey rounds. Most visit-pairs (72.4%) exhibited durable VLS, with few (2.5%) experiencing viral rebound. Among those with viremia at the initial visit (n=1,083), 46.9% maintained viremia through follow-up, 91.3% of which was high-level viremia. One-fifth (20.8%) of visit-pairs exhibiting persistent high-level viremia self-reported antiretroviral therapy (ART) use for >12 months. Prevalence of persistent high-level viremia varied substantially across communities and was significantly elevated among young persons aged 15-29 years (versus 40-49-year-olds; adjusted risk ratio [adjRR]=2.96; 95% confidence interval [95%CI]:2.21-3.96), men (versus women; adjRR=2.40, 95%CI:1.87-3.07), persons reporting inconsistent condom use with non-marital/casual partners (versus persons with marital/permanent partners only; adjRR=1.38, 95%CI:1.10-1.74), and persons exhibiting hazardous alcohol use (adjRR=1.09, 95%CI:1.03-1.16). The prevalence of persistent high-level viremia was highest among men <30 years (32.0%). Conclusions: Following universal ART provision, most persons living with HIV in south-central Uganda are durably suppressed. Among persons exhibiting viremia, nearly half maintain high-level viremia for >12 months and report higher-risk behaviors associated with onward HIV transmission. Enhanced linkage to HIV care and optimized treatment retention could accelerate momentum towards HIV epidemic control.

[1]  S. Odafe,et al.  Low-level viraemia among people living with HIV in Nigeria: a retrospective longitudinal cohort study , 2022, Lancet Global Health.

[2]  M. Lurie,et al.  Cyclical Engagement in HIV Care: A Qualitative Study of Clinic Transfers to Re-enter HIV Care in Cape Town, South Africa , 2022, AIDS and Behavior.

[3]  M. Siedner,et al.  Who’s slipping through the cracks? A comprehensive individual, clinical and health system characterization of people with virological failure on first‐line HIV treatment in Uganda and South Africa , 2021, HIV medicine.

[4]  L. A. Miller,et al.  Migration in Namibia and its association with HIV acquisition and treatment outcomes , 2021, PLoS ONE.

[5]  A. Raj,et al.  Alcohol use and alcohol-related consequences are associated with not being virally suppressed among persons living with HIV in the Rakai region of Uganda. , 2021, Drug and alcohol dependence.

[6]  C. Fraser,et al.  Age patterns of HIV incidence in eastern and southern Africa: a modelling analysis of observational population-based cohort studies , 2021, The lancet. HIV.

[7]  D. Barradas,et al.  Male partner age, viral load, and HIV infection in adolescent girls and young women: evidence from eight sub-Saharan African countries , 2021, AIDS.

[8]  W. Duffus,et al.  Sex Differences in HIV Testing — 20 PEPFAR-Supported Sub-Saharan African Countries, 2019 , 2020, MMWR. Morbidity and mortality weekly report.

[9]  T. Coates,et al.  Gendered health institutions: examining the organization of health services and men’s use of HIV testing in Malawi , 2020, Journal of the International AIDS Society.

[10]  D. Spiegelman,et al.  Integrating and Interpreting Findings from the Latest Treatment as Prevention Trials , 2020, Current HIV/AIDS Reports.

[11]  Irene N Njuguna,et al.  Clinic- and individual-level factors that influence HIV viral suppression in adolescents and young adults: a national survey in Kenya. , 2020, AIDS.

[12]  A. Sönnerborg,et al.  All-Cause Mortality and Serious Non-AIDS Events in Adults With Low-level Human Immunodeficiency Virus Viremia During Combination Antiretroviral Therapy: Results From a Swedish Nationwide Observational Study , 2020, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[13]  F. Giardina,et al.  Mapping and characterising areas with high levels of HIV transmission in sub-Saharan Africa: A geospatial analysis of national survey data , 2020, PLoS medicine.

[14]  P. Drain,et al.  Point-of-care HIV viral load testing combined with task shifting to improve treatment outcomes (STREAM): findings from an open-label, non-inferiority, randomised controlled trial. , 2020, The lancet. HIV.

[15]  J. Lessler,et al.  Migration, hotspots, and dispersal of HIV infection in Rakai, Uganda , 2020, Nature Communications.

[16]  S. Blower,et al.  HIV transmission and source-sink dynamics in sub-Saharan Africa. , 2020, The lancet. HIV.

[17]  Richard D Moore,et al.  Low level viremia and virologic failure in persons with HIV infection treated with antiretroviral therapy. , 2019, AIDS.

[18]  R. Hayes,et al.  Impact of a universal testing and treatment intervention on HIV incidence in Zambia and South Africa: results of the HPTN 071 (PopART) community-randomized trial , 2019, The New England Journal of Medicine.

[19]  M. J. van der Laan,et al.  HIV Testing and Treatment with the Use of a Community Health Approach in Rural Africa. , 2019, The New England journal of medicine.

[20]  E. T. Tchetgen Tchetgen,et al.  Universal Testing, Expanded Treatment, and Incidence of HIV Infection in Botswana. , 2019, The New England journal of medicine.

[21]  R. Hayes,et al.  Impact of a universal testing and treatment intervention on HIV incidence in Zambia and South Africa: results of the HPTN 071 (PopART) community-randomized trial , 2019, The New England journal of medicine.

[22]  F. Nalugoda,et al.  Intimate partner violence, HIV and sexually transmitted infections in fishing, trading and agrarian communities in Rakai, Uganda , 2019, BMC Public Health.

[23]  R. Fielding-Miller,et al.  A scoping review on the role of masculine norms in men’s engagement in the HIV care continuum in sub-Saharan Africa , 2019, AIDS care.

[24]  M. Petersen,et al.  Comparative assessment of five trials of universal HIV testing and treatment in sub‐Saharan Africa , 2018, Journal of the International AIDS Society.

[25]  N. McGrath,et al.  Universal test and treat and the HIV epidemic in rural South Africa: a phase 4, open-label, community cluster randomised trial. , 2017, The lancet. HIV.

[26]  N. Sewankambo,et al.  Combination HIV Prevention and HIV Incidence in Uganda , 2017, The New England Journal of Medicine.

[27]  W. El-Sadr,et al.  Selecting a viral load threshold for routine monitoring in resource‐limited settings: optimizing individual health and population impact , 2017, Journal of the International AIDS Society.

[28]  C. Beyrer,et al.  HIV Drug Resistance - An Emerging Threat to Epidemic Control. , 2017, The New England journal of medicine.

[29]  R. Gray,et al.  Rates of switching to second-line antiretroviral therapy and impact of delayed switching on immunologic, virologic, and mortality outcomes among HIV-infected adults with virologic failure in Rakai, Uganda , 2017, BMC Infectious Diseases.

[30]  J. Santelli,et al.  Mobility among youth in Rakai, Uganda: Trends, characteristics, and associations with behavioural risk factors for HIV , 2017, Global public health.

[31]  V. Falcó,et al.  HIV drug resistance in Africa: an emerging problem that deserves urgent attention. , 2017, AIDS.

[32]  S. Moore,et al.  Heterogeneity of the HIV epidemic in agrarian, trading, and fishing communities in Rakai, Uganda: an observational epidemiological study. , 2016, The lancet. HIV.

[33]  Pietro Vernazza,et al.  Sexual Activity Without Condoms and Risk of HIV Transmission in Serodifferent Couples When the HIV-Positive Partner Is Using Suppressive Antiretroviral Therapy. , 2016, JAMA.

[34]  T. Klimkait,et al.  Should viral load thresholds be lowered? , 2016, Medicine.

[35]  C. Beyrer,et al.  Marked sex differences in all-cause mortality on antiretroviral therapy in low- and middle-income countries: a systematic review and meta-analysis , 2016, Journal of the International AIDS Society.

[36]  D. Cummings,et al.  The Role of Viral Introductions in Sustaining Community-Based HIV Epidemics in Rural Uganda: Evidence from Spatial Clustering, Phylogenetics, and Egocentric Transmission Models , 2014, PLoS medicine.

[37]  R. Gray,et al.  Evaluation of current rapid HIV test algorithms in Rakai, Uganda. , 2013, Journal of virological methods.

[38]  R. Gray,et al.  A Qualitative Study of Barriers to Enrollment into Free HIV Care: Perspectives of Never-in-Care HIV-Positive Patients and Providers in Rakai, Uganda , 2013, BioMed research international.

[39]  R. Haubrich,et al.  Antiretroviral drug resistance in HIV-1-infected patients experiencing persistent low-level viremia during first-line therapy. , 2011, The Journal of infectious diseases.

[40]  Stephen R Cole,et al.  Constructing inverse probability weights for marginal structural models. , 2008, American journal of epidemiology.

[41]  W. Pan Akaike's Information Criterion in Generalized Estimating Equations , 2001, Biometrics.

[42]  L. Chang,et al.  Prevalence and Predictors of Persistent Human Immunodeficiency Virus Viremia and Viral Rebound After Universal Test and Treat: A Population-Based Study , 2021 .

[43]  R. Gray,et al.  Human immunodeficiency virus care cascade among sub‐populations in Rakai, Uganda: an observational study , 2017, Journal of the International AIDS Society.

[44]  S. Cole,et al.  Selection Bias Due to Loss to Follow Up in Cohort Studies. , 2016, Epidemiology.

[45]  N. Michael,et al.  Joint United Nations Programme on HIV/AIDS. , 2004, Military medicine.