Evidence map›Paper›PMID 37066200›Full record

ArticlemedRxiv : the preprint server for health sciences2023

sHIV-1 drug resistance in people on dolutegravir-based ART: Collaborative analysis of cohort studies.

Tom Loosli, Stefanie Hossmann, Suzanne M Ingle, Hajra Okhai, Katharina Kusejko, Johannes Mouton, Pantxika Bellecave, Ard van Sighem, Melanie Stecher, Antonella d'Arminio Monforte and 8 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. 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, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 9 institutions in 7 countries.

Tom LoosliDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland.
Stefanie HossmannInstitute of Social and Preventive Medicine (ISPM), University of Bern, Switzerland.
Suzanne M InglePopulation Health Sciences, Bristol Medical School, University of Bristol, UK.
Hajra OkhaiInstitute for Global Health, University College London, UK.
Katharina KusejkoDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland.
Johannes MoutonDepartment of Medicine, University of Cape Town, Cape Town, South Africa.
Pantxika BellecaveVirology laboratory, University Hospital Bordeaux, Bordeaux, France.
Ard van SighemStichting hiv monitoring, Amsterdam, the Netherlands.
Melanie StecherGerman Center for Infection Research (DZIF), Partner-Site Cologne-Bonn, Cologne, Germany.
Antonella d'Arminio MonforteItalian Cohort Naive Antiretrovirals, (ICONA) L'Azienda Socio Sanitaria Territoriale (ASST) Santi Paolo e Carlo, Milano, Italy.
M John GillSouthern Alberta Clinic, Calgary, AB, Canada.
Caroline A SabinInstitute for Global Health, University College London, UK.
Gary MaartensDepartment of Medicine, University of Cape Town, Cape Town, South Africa.
Huldrych F GünthardDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland.
Jonathan A C SternePopulation Health Sciences, Bristol Medical School, University of Bristol, UK.
Richard LessellsCentre for the AIDS Programme of Research in South Africa (CAPRISA), Durban, South Africa.
Matthias EggerInstitute of Social and Preventive Medicine (ISPM), University of Bern, Switzerland.
Roger KouyosDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland.
University of Zurich · CHUniversity of Cape Town · ZAUniversity College London · GBUniversity of Bern · CHUniversity of Bristol · GBAzienda Socio Sanitaria Territoriale Lariana · ITStichting HIV Monitoring · NLUniversity of Calgary · CAUniversity of Cologne · DE

Funding

Observational Antiretroviral Studies In Southern Africa (OASIS) CollaborationU01AI069924 · NIAID · UNIVERSITAT BERN · PI Cleophas Chimbetete, Mary-Ann Davies · 2006 to 2026
$55.9M
A Randomized Clinical Trial to Evaluate Solutions for the Management of Virologic Failure for Individuals on TLD in Sub-Saharan AfricaR01AI167699 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Suzanne McCluskey · 2022 to 2026
$3.4M
HIV-1 subtype-specific drug resistance in patients failing Dolutegravir-based 1st, 2nd or 3rd line regimens: the International epidemiological Databases to Evaluate AIDS (IeDEA)R01AI152772 · NIAID · UNIVERSITY OF ZURICH · PI Roger Dimitri Kouyos · 2021 to 2026
$3.2M
1/3 Collaborative Research in HIV/AIDS, Alcohol, and Related Comorbidities (COMpAAAS) Tripartite: ART-CC, KP, and VAU01AA026209 · NIAAA · UNIVERSITY OF BRISTOL · PI STERNE, JONATHAN · 2017 to 2021
$2.2M
Medical Research Council MR/M004236/1NIAAA NIH HHS U01 AA026209NIAID NIH HHS R01 AI152772NIAID NIH HHS R01 AI167699NIAID NIH HHS U01 AI069924
6 · The paper itself

Abstract

Background: The widespread use of the integrase strand transfer inhibitor (INSTI) dolutegravir (DTG) in first- and second-line antiretroviral therapy (ART) may facilitate emerging resistance. We combined data from HIV cohorts to examine patterns of drug resistance mutations (DRMs) and identify risk factors for DTG resistance. Methods: Eight cohorts from Canada, Europe, and South Africa contributed data on individuals with genotypic resistance testing on DTG-based ART. Resistance levels were categorised using the Stanford algorithm. We identified risk factors for resistance using mixed-effects ordinal logistic regression models. Results: We included 750 people with genotypic resistance testing on DTG-based ART between 2013 and 2022. Most had HIV subtype B (N=444, 59·2%) and were treatment-experienced; 134 (17.9%) were on DTG dual and 19 (2.5%) on DTG monotherapy. INSTI DRMs were detected in 100 (13·3%) individuals; 21 (2·8%) had more than one mutation. Most (N=713, 95·1%) were susceptible to DTG, 8 (1·1%) had potential-low, 5 (0·7%) low, 18 (2·4%) intermediate and 6 (0·8%) high-level DTG resistance. The risk of DTG resistance was higher on DTG monotherapy (adjusted odds ratio (aOR) 37·25, 95% CI 11·17 to 124·2) and DTG lamivudine dual therapy (aOR 6·59, 95% CI 1·70 to 25·55) compared to combination ART, and higher in the presence of potential-low/low (aOR 4.62, 95% CI 1.24 to 17.2) or intermediate/high-level (aOR 7·01, 95% CI 2·52 to 19·48) nucleoside reverse transcriptase inhibitors (NRTI) resistance. Viral load on DTG showed a trend towards increased DTG resistance (aOR 1·42, 95% CI 0·92 to 2·19 per standard deviation of log Interpretation: Among people experiencing virological failure on DTG-based ART, INSTI DRMs were uncommon, and DTG resistance was rare. DTG monotherapy and NRTI resistance substantially increased the risk for DTG resistance, which is of concern, notably in resource-limited settings.

Identifiers

PMID37066200
PMCPMC10104228
OpenAlexW4362636282

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Registered trials

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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.