Evidence map›Paper›PMID 41867239›Full record

ArticlemedRxiv : the preprint server for health sciences2026

HIV viral non-suppression and drug resistance among persons who inject drugs on dolutegravir antiretroviral therapy in Kenya.

Loice W Mbogo, Ceejay L Boyce, Betsy Sambai, Stephen E Hawes, Brandon L Guthrie, William Sinkele D Min, David Kimani, Vincent Adhanja, Bhavna H Chohan, Robert A Smith and 8 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Loice W MbogoUniversity of Washington Global Assistance Program-Kenya, Nairobi, Kenya.ORCID 0000-0001-5916-7188
Ceejay L BoyceCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.ORCID 0000-0002-3716-8216
Betsy SambaiUniversity of Washington Global Assistance Program-Kenya, Nairobi, Kenya.
Stephen E HawesDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, USA.ORCID 0000-0002-3361-6026
Brandon L GuthrieDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, USA.
William Sinkele D MinNational HIV and STI Control Programme (NASCOP), Kenya Ministry of Health, Nairobi, Kenya.ORCID 0000-0001-6898-207X
David KimaniUniversity of Washington Global Assistance Program-Kenya, Nairobi, Kenya.
Vincent AdhanjaUniversity of Washington Global Assistance Program-Kenya, Nairobi, Kenya.
Bhavna H ChohanDepartment of Global Health, University of Washington, Seattle, USA School of Public Health and School of Medicine, University of Washington, Seattle, USA.ORCID 0000-0002-2125-6799
Robert A SmithDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, USA.ORCID 0000-0003-3202-1650
Aliza Monroe-WiseDepartment of Global Health, University of Washington, Seattle, USA School of Public Health and School of Medicine, University of Washington, Seattle, USA.
Esther GitauSupport for Addictions Prevention and Treatment in Africa (SAPTA), Nairobi, Kenya.
Sarah MasyukoDepartment of Global Health, University of Washington, Seattle, USA School of Public Health and School of Medicine, University of Washington, Seattle, USA.
Vincent C MarconiDivision of Infectious Diseases Emory University School of Medicine and Department of Global Health, Emory University, Atlanta, USA.ORCID 0000-0001-8409-4689
Geoffrey S GottliebDepartment of Global Health, University of Washington, Seattle, USA School of Public Health and School of Medicine, University of Washington, Seattle, USA.ORCID 0000-0002-5749-481X
Paul K DrainDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, USA.
Lisa M FrenkelCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.
Carey FarquharDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, USA.

Funding

Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
Drug Resistance Genotypic and Phenotypic Correlates of Efavirenz and Dolutegravir based Treatment Outcomes across Non-B HIV-1 subtypesR01AI147309 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI DRAIN, PAUL K, FRENKEL, LISA M · 2019 to 2023
$4.6M
Integrating Assisted Partner Services and Phylogenetics for HIV and HCV PreventionR01DA043409 · NIDA · UNIVERSITY OF WASHINGTON · PI FARQUHAR, CAREY, HERBECK, JOSHUA T · 2017 to 2021
$3.6M
NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI147309NIDA NIH HHS R01 DA043409
6 · The paper itself

Abstract

Background: Maintaining viral suppression among people who inject drugs ( Methods: We enrolled Kenyan PWID who had transitioned from an efavirenz ( Results: Among 250 participants, 125 were receiving methadone, 199 (79.6) reported heroin use, 70% were male, and median age was 39 years. 194 (77.6%) participants completed all five study visits, 41 (16.4%) were lost to follow-up and 15 (6.0%) died. Across all study visits, 166 (66.0%) of the 250 participants were always suppressed, and 84 (33.6%) were viremic at least once during follow-up, including 8 (3.2%) who were always viremic and 76 (30.4%) who were intermittently suppressed. Living in an improvised shelter or outdoors was significantly associated with a higher risk of viremia (HR=4.35, 95% CI: 1.52-12.53). 93 specimens had drug resistance genotyping, 27 (29%) of which were from participants with incomplete follow-up. NNRTI resistance was frequent (37-41% across visits), whereas major resistance mutations were infrequent to tenofovir (4.3%), lamivudine (7.5%), and DTG (1%, minority variant S153F detected at 1% frequency). Accessory DTG mutations, which do not independently reduce susceptibility, were more common, observed in 41% (38/93) of genotyped specimens, most often T97A, E138K, and L74M. Conclusion: Among PWID living with HIV on TLD in Kenya, one-third had intermittent or sustained viral non-suppression across two years of follow-up. While NNRTI resistance was common, DTG resistance mutations were rare. Improving viral suppression among PWID living with HIV will reduce transmission risks and improve clinical outcomes.

Indexed as

antiretroviral therapy (ART)dolutegravirdrug resistancelongitudinal cohort studyPersons who inject drugs (PWID)viral non-suppression

Identifiers

PMID41867239
PMCPMC13004105

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.