Evidence map›Paper›PMID 37539492›Full record

ArticleThe Journal of antimicrobial chemotherapy2023

Long-term effects on subclinical cardiovascular disease of switching from boosted protease inhibitors to dolutegravir.

Ana González-Cordón, Lambert Assoumou, Graeme Moyle, Laura Waters, Margaret Johnson, Pere Domingo, Julie Fox, Hans-Jürgen Stellbrink, Giovanni Guaraldi, Mar Masiá and 10 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

20 authors at 15 institutions in 6 countries.

Ana González-CordónHospital Clínic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Lambert AssoumouINSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique, Sorbonne Université, Paris, France.
Graeme MoyleConsultant Physician in HIV Medicine, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
Laura WatersMortimer Market Centre, Central and North West London NHS Foundation Trust, London, UK.
Margaret JohnsonSenior Consultant Physician in Thoracic Medicine, Royal Free London NHS Foundation Trust, London, UK.
Pere DomingoCIBER de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0003-1138-5770
Julie FoxHIV Research Lead, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Hans-Jürgen StellbrinkProfessor of Medicine, Infektionsmedizinisches Centrum, Hamburg, Germany.
Giovanni GuaraldiProfessor of Medicine, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-5724-3914
Mar MasiáCIBER de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0001-9878-2458
Mark GompelsClinical Lead for Allergy, Immunology and HIV, North Bristol NHS Trust, Bristol, UK.
Stephane De WitProfessor of Medicine, Centre Hospitalier Universitaire Saint-Pierre, Brussels, Belgium.
Eric FlorenceHead of the HIV Clinic, Universitair Ziekenhuis Antwerpen, Antwerp, Belgium.
Stefan EsserAcademic Director, Universitätsklinikum, Essen, Germany.
François RaffiProfessor of Infectious Diseases, Centre Hospitalier Universitaire, Nantes, France.
Georg BehrensProfesor of Immunology, Medizinische Hochschule, Hannover, Germany.
Anton PozniakConsultant Physician in HIV Medicine, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
Jose M GatellGlobal Medical Director, ViiV Healthcare, Brentford, UK.
Esteban MartínezHospital Clínic-IDIBAPS, University of Barcelona, Barcelona, Spain.
NEAT 022 Study Group
Instituto de Salud Carlos III · ESChelsea and Westminster Hospital NHS Foundation Trust · GBAntwerp University Hospital · BECentral and North West London NHS Foundation Trust · GBCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Saint-Pierre · BEEssen University Hospital · DEGuy's and St Thomas' NHS Foundation Trust · GBInfektionsmedizinisches Centrum Hamburg · DEMedizinische Hochschule Hannover · DENorth Bristol NHS Trust · GBRoyal Free London NHS Foundation Trust · GBUniversity of Modena and Reggio Emilia · ITViiV Healthcare (United Kingdom) · GBInserm · FR

Funding

Medical Research Council MC_UU_00004/03Medical Research Council MC_UU_12023/2Medical Research Council MC_UU_12023/23
6 · The paper itself

Abstract

backgroundIn the NEAT022 trial, switching from boosted PIs (PI/r) to dolutegravir in people with HIV (PWH) with high cardiovascular risk decreased plasma lipids, soluble CD14 and adiponectin, and showed consistent favourable, although non-significant, effects on carotid intima-media thickness (CIMT) progression at 48 weeks. We hereby communicate planned final 96 week results on biomarker changes and CIMT progression.

methodsPWH on a PI/r-based triple therapy regimen were randomly assigned (1:1) to switch the PI/r component to dolutegravir either immediately (DTG-I group) or after 48 weeks (DTG-D group) and were followed up to 96 weeks. We assessed changes in biomarkers associated with inflammation, endothelial dysfunction, monocyte immune activation, oxidation, insulin resistance, hypercoagulability, heart failure, myocardial injury and glomerular and tubular kidney injury, and right and left CIMT progression at 48 and 96 weeks.

resultsOf 415 PWH randomized, 287 (69%) and 143 (34%) contributed to the biomarker and CIMT substudies respectively. There were significant 96 week changes in biomarkers associated with inflammation, immune activation, oxidation, insulin resistance and myocardial injury. Most changes were favourable, except for adiponectin reduction, which may suggest higher insulin resistance. We were unable to detect significant changes in the progression of CIMT between arms or within arms at 96 weeks. DISCUSSION: After 96 weeks, switching from PI/r to dolutegravir in PWH with high cardiovascular risk led to significant changes in several biomarkers associated with cardiovascular disease. Although most changes were favourable, adiponectin reduction was not. There were non-significant changes in CIMT progression.

Indexed as

Anti-HIV AgentsCardiovascular DiseasesHIV InfectionsHIV Protease InhibitorsInsulin ResistanceAdiponectinBiomarkersCarotid Intima-Media ThicknessDolutegravirHumansInflammationAdiponectinAnti-HIV AgentsBiomarkersDolutegravirHIV Protease Inhibitors

Identifiers

PMID37539492
PMCPMC7617418
OpenAlexW4385562416

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.