Evidence map›Paper›PMID 37052343›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

Plasma Human Immunodeficiency Virus 1 RNA and CD4+ T-Cell Counts Are Determinants of Virological Nonsuppression Outcomes With Initial Integrase Inhibitor-Based Regimens: A Prospective RESPOND Cohort Study.

Hortensia Álvarez, Amanda Mocroft, Lene Ryom, Bastian Neesgaard, Simon Edwards, Veronica Svedhem, Huldrych F Günthard, Robert Zangerle, Colette Smith, Antonella Castagna and 23 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% of its field
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Virologic Failure and Emergent Integrase Strand Transfer Inhibitor Drug Resistance With Long-Acting Cabotegravir for HIV Treatment: A Meta-analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
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  15. Laboratory Report of HIV-1 Low-Level Viremia.Open forum infectious diseases · 2024
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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

33 authors at 20 institutions in 14 countries.

Hortensia ÁlvarezDepartment of Internal Medicine, Infectious Diseases Unit, Complexo Hospitalario Universitario de Ferrol, Ferrol, SERGAS-A Coruña, Spain.ORCID 0000-0002-5002-1737
Amanda MocroftCHIP, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Lene RyomCHIP, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Bastian NeesgaardCHIP, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Simon EdwardsDepartment of HIV, Mortimer Market Centre, London, United Kingdom.
Veronica SvedhemDepartment of Medicine, Medical Unit Infectious Diseases, Karolinska University Hospital, Karolinska Institutet, Huddinge, Sweden.
Huldrych F GünthardDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich and Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
Robert ZangerleAustrian HIV Cohort Study, Medizinische Universität Innsbruck, Innsbruck, Austria.
Colette SmithThe Royal Free HIV Cohort Study, Royal Free Hospital, University College London, London, United Kingdom.
Antonella CastagnaSan Raffaele Scientific Institute, Università Vita-Salute San Raffaele, Milano, Italy.
Antonella d'Arminio MonforteItalian Cohort Naive Antiretrovirals (ICONA), ASST Santi Paolo e Carlo, Milano, Italy.
Ferdinand WitAIDS Therapy Evaluation in the Netherlands (ATHENA) cohort, HIV Monitoring Foundation, Amsterdam, The Netherlands.
Melanie StecherDivision of Infectious Diseases, Department I of Internal Medicine, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID 0000-0002-3460-1299
Clara LehmanDivision of Infectious Diseases, Department I of Internal Medicine, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.
Cristina MussiniModena HIV Cohort, Università degli Studi di Modena, Modena, Italy.
Eric FontasNice HIV Cohort, Université Côte d´Azur et Centre Hospitalier Universitaire, Nice, France.
Eva GonzálezPISCIS Cohort Study, Centre Estudis Epidemologics de ITS i VIH de Catalunya, Badalona, Spain.
Jan-Christian WasmuthMedical Department, University Hospital Bonn, Bonn, Germany.
Anders SönnerborgSwedish InfCare HIV Cohort, Karolinska University Hospital, Stockholm, Sweden.
Stéphane De WitCHU Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.
Nikoloz ChkhartishviliGeorgian National AIDS Health Information System, Infectious Diseases, AIDS and Clinical Immunology Research Center, Tbilisi, Georgia.
Christoph StephanFrankfurt HIV Cohort Study, University Hospital Frankfurt, Goethe-University, Infectious Diseases Unit, Frankfurt, Germany.
Kathy PetoumenosThe Kirby Institute, University of New South Wales, Sydney, Australia.
Nadine JaschinskiCHIP, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Vani VannappagariViiV Healthcare, Research Triangle Park, North Carolina, USA.
Joel GallantGilead Sciences, Foster City, California, USA.
Lital YoungMerck Sharp & Dohme, Luzern, Switzerland.
Alain Volny AnneEuropean AIDS Treatment Group, Brussels, Belgium.
Lauren GreenbergCHIP, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Raquel Martín-IguacelInfectious Diseases Department, Odense University Hospital, Odense, Denmark.
Eva PovedaGroup of Virology and Pathogenesis, Galicia Sur Health Research Institute (IIS Galicia Sur)-Complexo Hospitalario Universitario de Vigo, Vigo, SERGAS-UVigo, Spain.ORCID 0000-0003-4835-9875
Josep M LlibreInfectious Diseases Division and Fight Infections Foundation, University Hospital Germans Trias i Pujol, Barcelona, Spain.
RESPOND (International Cohort Consortium of Infectious Diseases) Study Group
Fundació Lluita contra les Infeccions · ESOdense University Hospital · DKUniversity of Copenhagen · DKComplexo Hospitalario Universitario A Coruña · ESUNSW Sydney · AUInnsbruck Medical University · ATKarolinska University Hospital · SEUniversité Côte d'Azur · FRUniversité Libre de Bruxelles · BEAIDS and Clinical Immunology Research Center · GEStichting HIV Monitoring · NLThe Royal Free Hospital · GBUniversity Hospital Bonn · DEUniversity of Modena and Reggio Emilia · ITUniversity of Zurich · CHVita-Salute San Raffaele University · ITAzienda Socio Sanitaria Territoriale Santi Paolo e CarloGoethe University Frankfurt · DEMSD (Switzerland) · CHEuropean Organisation for Research and Treatment of Cancer · BE

Funding

The Asia-Pacific HIV Research CollaborationU01AI069907 · NIAID · FOUNDATION FOR AIDS RESEARCH · PI ANNETTE H SOHN · 2006 to 2026
$44.8M
NIAID NIH HHS U01 AI069907
6 · The paper itself

Abstract

backgroundThere are conflicting data regarding baseline determinants of virological nonsuppression outcomes in persons with human immunodeficiency virus (HIV) starting antiretroviral treatment (ART). We evaluated the impact of different baseline variables in the RESPOND cohort.

methodsWe included treatment-naive participants aged ≥18 who initiated 3-drug ART, in 2014-2020. We assessed the odds of virological suppression (VS) at weeks 48 and 96 using logistic regression. Viral blips, low-level viremia (LLV), residual viremia (RV), and virological failure (VF) rates were assessed using Cox regression.

resultsOf 4310 eligible participants, 72% started integrase strand transfer inhibitor (INSTI)-based regimens. At 48 and 96 weeks, 91.0% and 93.3% achieved VS, respectively. At 48 weeks, Kaplan-Meier estimates of rates were 9.6% for viral blips, 2.1% for LLV, 22.2% for RV, and 2.1% for VF. Baseline HIV-1 RNA levels >100 000 copies/mL and CD4+ T-cell counts ≤200/µL were negatively associated with VS at weeks 48 (adjusted odds ratio, 0.51 [95% confidence interval, .39-.68] and .40 [.27-.58], respectively) and 96 and with significantly higher rates of blips, LLV, and RV. CD4+ T-cell counts ≤200/µL were associated with higher risk of VF (adjusted hazard ratio, 3.12 [95% confidence interval, 2.02-4.83]). Results were consistent in those starting INSTIs versus other regimens and those starting dolutegravir versus other INSTIs.

conclusionsInitial high HIV-1 RNA and low CD4+ T-cell counts are associated with lower rates of VS at 48 and 96 weeks and higher rates of viral blips, LLV, and RV. Low baseline CD4+ T-cell counts are associated with higher VF rates. These associations remain with INSTI-based and specifically with dolutegravir-based regimens. These findings suggest that the impact of these baseline determinants is independent of the ART regimen initiated.

Indexed as

HIV-1HIV InfectionsHIV Integrase InhibitorsRNA, ViralCD4-Positive T-LymphocytesCohort StudiesHumansProspective StudiesViral LoadViremiaHIV Integrase InhibitorsRNA, Viralblipintegrase inhibitorslow-level viremiaresidual viremiavirological failure

Identifiers

PMID37052343
PMCPMC10893964
OpenAlexW4365442995

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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.