Evidence map›Paper›PMID 39450853›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

No accelerated progression of subclinical atherosclerosis with integrase strand transfer inhibitors compared to non-nucleoside reverse transcriptase inhibitors.

Javier García-Abellán, José A García, Sergio Padilla, Marta Fernández-González, Vanesa Agulló, Paula Mascarell, Ángela Botella, Félix Gutiérrez, Mar Masiá

Abstract readComparative Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Javier García-AbellánInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.ORCID 0000-0002-5217-3726
José A GarcíaInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.ORCID 0000-0002-1203-7260
Sergio PadillaInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.ORCID 0000-0002-8420-7310
Marta Fernández-GonzálezCIBER de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0001-9949-8504
Vanesa AgullóInfectious Diseases Unit, Hospital General Universitario de Elche, Alicante, Spain.ORCID 0000-0002-7036-2184
Paula MascarellInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.ORCID 0000-0002-0566-0935
Ángela BotellaInfectious Diseases Unit, Hospital General Universitario de Elche, Alicante, Spain.
Félix GutiérrezInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.
Mar MasiáInfectious Diseases Unit, Hospital General Universitario de Elche and Universidad Miguel Hernández de Elche, Alicante, Spain.ORCID 0000-0001-9878-2458

Funding

Conselleria de Innovación, Universidades, Ciencia y Sociedad Digital, Generalitat Valenciana AICO/2021/205Consorcio Centro de Investigación Biomédica en RedEuropean Regional Development FundGeneralitat Valenciana A-32 2020Instituto de Salud Carlos III PI16/01740Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and European Union-NextGenerationEU CB21/13/00011Spanish National Plan for Scientific and Technical Research and InnovationUMH-FISABIO
6 · The paper itself

Abstract

backgroundThe role of integrase strand transfer inhibitors (INSTI) in the cardiovascular risk of people with HIV is controversial.

objectivesTo assess the association of INSTI to subclinical atherosclerosis progression measured with the carotid intima-media thickness (cIMT).

methodsProspective study in virologically suppressed people with HIV receiving INSTI- or NNRTI-based regimens. cIMT was measured at baseline, 48 and 96 weeks. cIMT progression was analysed both as a continuous and categorical variable, defined as cIMT increase ≥ 10% and/or new carotid plaque. Adjustments through Cox proportional hazard regression and linear mixed models, and propensity score matching were conducted.

results190 participants were recruited and 173 completed the 96 week follow-up. 107 (56.3%) were receiving an INSTI-containing, 128 (67.4%) a NNRTI-containing and 45 (23.7%) a NNRTI plus an INSTI-containing regimen. The overall median (IQR) 2-year change of cIMT was 0.029 (-0.041 to 0.124) mm; 87 (45.8%) participants experienced a cIMT increase ≥ 10%, of whom 54 (28.4%) developed a new carotid plaque. Adjusted Cox regression showed no differences between INSTI and NNRTI groups in the categorical 2-year progression of cIMT, both including or excluding participants receiving INSTI + NNRTI. Similar results were observed for the continuous cIMT increase through adjusted linear mixed models. Propensity score matching showed no significant differences in the 2 year cIMT change between treatment groups [0.049 mm (-0.031-0.103) in the INSTI group versus 0.047 mm (-0.023-0.115) in the NNRTI group; P = 0.647]. cIMT progression was associated with traditional cardiovascular risk factors.

conclusionsINSTI-based regimens are not associated with increased progression of subclinical atherosclerosis when compared to NNRTI.

Indexed as

AtherosclerosisCarotid Intima-Media ThicknessDisease ProgressionHIV InfectionsReverse Transcriptase InhibitorsAdultFemaleHIV Integrase InhibitorsHumansMaleMiddle AgedProspective StudiesHIV Integrase InhibitorsReverse Transcriptase Inhibitors

Identifiers

PMID39450853
PMCPMC11695909

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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.