Evidence map›Paper›PMID 37637394›Full record

ArticleThe Pan African medical journal2023

[Interventional study on Dolutegravir and other antiretrovirals in patients with subclinical atherosclerosis in the Kinshasa Hospital].

Murielle Longokolo Mashi, Marcel Mbula Mambimbi, Hippolyte Nani-Tuma Situakibanza, Madone Mandina Ndona, Jean-Robert Makulo Risassi, Nadine Mayasi Ngongo, Ben Bepouka, Odio Ossam, Jean Mukaya Tshibola, Frédéric Tshibasu Tshienda and 7 more

Open access · goldAbstract readEnglish Abstract
In one paragraph

Article in The Pan African medical journal, 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
0.3field-weighted citation impact, top 40% 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, 1 citations in OpenAlex.

  1. Article
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

17 authors at 1 institution in 1 country.

Murielle Longokolo MashiService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Marcel Mbula MambimbiService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Hippolyte Nani-Tuma SituakibanzaService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Madone Mandina NdonaService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Jean-Robert Makulo RisassiService de Néphrologie, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Nadine Mayasi NgongoService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Ben BepoukaService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Odio OssamService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Jean Mukaya TshibolaDépartement de Radiologie, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Frédéric Tshibasu TshiendaDépartement de Radiologie, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Eric Mukenge KasongoService de Biologie Clinique, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Mamy Ngole NzitaService de Biologie Clinique, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Lukiana TunaService de Biologie Clinique, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Aimée LuleboÉcole de Santé Publique, Université de Kinshasa, République Démocratique du Congo.
Donatien Mangala SonziService des Maladies infectieuses, Cliniques Universitaires de Kinshasa, Kinshasa, République Démocratique du Congo.
Christian Kisoka LusunsiDepartment of Public Health, Lomo University of Research, Kinshasa, Democratic Republic of Congo.
Benjamin Longo-MbenzaDepartment of Public Health, Lomo University of Research, Kinshasa, Democratic Republic of Congo.
University of Kinshasa · CD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: After 2016, the World Health Organization (WHO) proposed Dolutegravir (DTG) as an alternative first-line treatment for adults. Thus, the purpose of this study was to identify biomarkers of cardiometabolic risk capable of demonstrating the beneficial effect of Dolutegravir (DTG) compared to other antiretrovirals in predicting atherosclerosis in people living with HIV (PLHIV) and hospitalized in Kinshasa Hospital. Methods: we conducted an interventional study of people living with HIV who had received antiretroviral therapy (ART) for at least 6 months and were treated in the structures of the network coordinated by the Catholic Church (BDOM-Bureau Diocésain des Oeuvres Médicales) and of the University Clinics of Kinshasa (CUK) between January 2017 and December 2021. Subclinical atherosclerosis was defined as Pulsed Pressure (PP) ≥60 mm Hg; Carotid Intima-Media Thickness (CIMT) > 0.8 mm; and Systolic Pressure Index (SPI) < 0.9. Logistic regression was used in the statistical analysis of associations. Results: a total of 334 PLHIV were recruited, of whom 96.1% (n=321) were on ART and 13.9% (n=13) were ART naïve patients. The mean age of PLHIV was 51±12 years with a female predominance (70.4%; n=235); the independent determinants of subclinical atherosclerosis were marital status (aOR: 4. 95% CI 1.5-10.5; p<0.006), low socioeconomic level (aOR: 10.7, 95% CI 2.3-48.7 p<0.002), duration of HIV infection (aOR: 6.6, 95% CI 2.8-16; p<0.0001), duration of antiretroviral therapy ≥9 years (aOR: 0.3, 95% CI 0.2-0.7; p<0.005) and total cholesterol ratio/high-density lipoprotein-cholesterol (CT/HDL-c)(aOR: 2, 95% CI 1.1-3.6; p= 0.034). The mean values of traditional and emergent variables were significantly higher in the previous ART regimen without DTG than in the new regimen with DTG. However, dyslipidemia was detected during the new DTG-based regimen. Conclusion: dyslipidemia was common during the DTG-based regimen. Marital status, low socioeconomic level, duration of HIV infection, duration of antiretroviral treatment beyond 9 years and the TC/HDL-c ratio were identified as determinants of subclinical atherosclerosis in PLHIV on ART hospitalized in the Kinshasa hospital.

Indexed as

AtherosclerosisHIV InfectionsAdultAnti-Retroviral AgentsCarotid Intima-Media ThicknessCholesterol, HDLDemocratic Republic of the CongoDolutegravirFemaleHospitalsHumansMaleMiddle AgedResearch DesignAnti-Retroviral AgentsCholesterol, HDLDolutegravirantiretroviral therapyDemocratic Republic of CongoHIV/AIDSKinshasaSubclinical atherosclerosis

Identifiers

PMID37637394
PMCPMC10460102
OpenAlexW4378472914

What OpenQuestion holds

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LicenceCC BY
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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.