Evidence map›Paper›PMID 42609932›Full record

ArticleOpen forum infectious diseases2026

Cardiovascular Disease Risk with Integrase Inhibitor-based Antiretroviral Therapy: A Causal Inference Analysis in RESPOND.

Bernard Surial, Bastian Neesgaard, Frédérique Chammartin, Lene Ryom, Kathy Petoumenos, Joanne Reekie, Roger Paredes, Robert Zangerle, Colette Smith, Charlotte Martin and 17 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 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

27 authors.

Bernard SurialDepartment of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0002-1402-974X
Bastian NeesgaardCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Frédérique ChammartinDivision of Clinical Epidemiology, Department of Clinical Research, University Hospital and University of Basel, Basel, Switzerland.
Lene RyomDepartment of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Kathy PetoumenosThe Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
Joanne ReekieCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-8529-3559
Roger ParedesDepartment of Infectious Diseases, Hospital Universitari Germans Trias I Pujol, Badalona, Spain.ORCID https://orcid.org/0000-0002-6553-691X
Robert ZangerleDepartment of Dermatology, Venereology, and Allergy, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-5375-7299
Colette SmithThe Royal Free HIV Cohort Study, Royal Free Hospital, University College London, London, UK.
Charlotte MartinInfectious Diseases Department, CHU Saint-Pierre, Université Libre de Bruxelles (ULB), Brussels, Belgium.ORCID https://orcid.org/0000-0002-8995-6230
Ferdinand WitAIDS Therapy Evaluation in the Netherlands (ATHENA) Cohort, HIV Monitoring Foundation, Amsterdam, The Netherlands.
Nadine JaschinskiCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Cristina MussiniModena HIV Cohort, Università degli Studi di Modena, Modena, Italy.
Antonella d'Arminio MonforteIcona Foundation, Milan, Italy.
Antonella CastagnaIcona Foundation, Milan, Italy.ORCID https://orcid.org/0000-0002-8338-9714
Christina CarlanderDepartment of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0001-9962-5964
Larysa HetmanPublic Health Center of Ukraine, Ministry of Health, Kyiv, Kyiv Oblast, Ukraine.
Elena SohaniDepartment of Dermatology, Venereology, and Allergy, Medical University Innsbruck, Innsbruck, Austria.
Clara LehmannDepartment I of Internal Medicine, Division of Infectious Diseases, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.
Sean R HoseinEuropean AIDS Treatment Group, Brussels, Belgium.
Jean Andre Van WykViiV Healthcare, London, UK.
Emiliano BissioMerck & Co., Inc., Rahway, New Jersey, USA.
Jens LundgrenCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-8901-7850
Andri RauchDepartment of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0001-5297-6062
Huldrych F GünthardDepartment of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0002-1142-6723
Gilles WandelerDepartment of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0002-5278-8763
Lauren GreenbergCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A previous RESPOND analysis suggested that integrase inhibitors (INSTIs) increase cardiovascular disease (CVD) risk compared with other antiretroviral therapy (ART). We reanalyzed the data using target trial emulations examining the impact of methodological choices. Methods: Treatment-naïve analyses included ART-naïve adults with detectable HIV viraemia and recent CD4 and HIV-RNA measurements. Treatment-experienced analyses included adults with suppressed HIV-RNA receiving INSTI-free ART. We estimated adjusted risk differences (RDs) and risk ratios (RRs) for CVD events comparing INSTI initiation or switching versus other ART using inverse-probability weighting and pooled logistic regression. Results: Among 7111 treatment-naïve individuals, 95 CVD events occurred over a median of 62 months. Risk ratios comparing INSTI initiation with starting other ART were 1.07 (95% confidence interval .29-4.93) at 1 year, 1.21 (.41-3.91) at 2 years, and 1.87 (1.06-3.26) at 6 years. Corresponding RDs were 0.02% (-.32-.29), 0.09% (-.43-.53), and 1.03% (0.08-2.07). Among 22 921 treatment-experienced individuals, 800 CVD events occurred over a median of 37 months. Risk ratios were 1.55 (1.16-2.00) at 1 year, 1.30 (1.07-1.62) at 2 years, and 0.93 (.78-1.09) at 6 years. Corresponding RDs were 0.26% (.08-.47), 0.29% (.03-.58), and -0.22 (-.66-.25). Conclusions: Switching to INSTIs was associated with a transient increase in CVD risk during the first 2 years among treatment-experienced individuals, whereas starting INSTIs in ART-naïve individuals was associated with a gradual increase over time, albeit based on few events. Absolute RDs remained small, but the findings suggest a potential impact of INSTIs on the development of CVD.

Indexed as

cardiovascular diseaseHIVintegrase inhibitorstarget trial emulation

Identifiers

PMID42609932
PMCPMC13479176

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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.