Evidence map›Paper›PMID 41966981›Full record

ArticleThe Journal of infectious diseases2026

Plasma GDF-15 Levels Are Associated With HIV Reservoir Markers Independently of Inflammation in People With HIV on Antiretroviral Therapy.

Stephane Isnard, Léna Royston, Carolina A Berini, Tsoarello Mabanga, Abdulrahman Al-Abdulmalek, Orthy Aiyana, Liqin Sun, Mohamed El-Far, Amélie Pagliuzza, Delphine Planas and 7 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Stephane IsnardResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Léna RoystonResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.ORCID 0000-0003-2367-7682
Carolina A BeriniResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Tsoarello MabangaResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Abdulrahman Al-AbdulmalekResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.ORCID 0000-0002-9814-2925
Orthy AiyanaResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Liqin SunResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Mohamed El-FarCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.
Amélie PagliuzzaCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.ORCID 0000-0001-8124-2607
Delphine PlanasCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.
Simeng BuResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Meetinder Kaur PardesiResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.
Rémi FromentinCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.ORCID 0000-0002-8153-1799
Petronela AncutaCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.
Madeleine DurandDépartement de Microbiologie, Infectiologie et Immunologie, Faculté de Médecine, Université de Montréal, Montréal, Québec, Canada.ORCID 0000-0002-9459-9549
Nicolas ChomontCentre de Recherche du Centre Hospitalier de l'Université de Montréal,Montréal, Québec, Canada.ORCID 0000-0001-9747-5018
Jean-Pierre RoutyResearch Institute, McGill University Health Centre, Montréal, Québec, Canada.ORCID 0000-0001-9897-7589

Funding

Role of IL-32 as a predictor and mediator of Premature Aging Phenotypes(PAP) in HIV infection.R01AG054324 · NIA · CENTRE HOSPITALIER DE L'UNIVERSITE DE MONTREAL (UNIVERSITY OF MONTREAL HOSPITAL) · PI TREMBLAY, CECILE · 2016 to 2025
$4.2M
Canadian Foundation for AIDS Research 02-512Canadian HIV and Aging Cohort StudyCIHR 103230CIHR 284512CIHR 364423CIHR 398643CIHR 399544CIHR BR4-197730CIHR DCO150GPCIHR PJT 166049CIHR Canadian HIV Trials Network CTN 257CIHR Canadian HIV Trials Network CTN 272Clinical Care Management CoreDépartement de RadiologieFonds de la Recherche Québec-SantéFRQS-SIDA Maladies Infectieuses NetworkMaladies Infectieuses and Thérapie Cellulaire; Réseau de Bioimagerie du Québec MOP 103230Maladies Infectieuses and Thérapie Cellulaire; Réseau de Bioimagerie du Québec PTJ 166049NIA NIH HHS R01 AG054324NIH HHS R01AG054324Radio-Oncologie et Médecine NucléaireRéseau SIDAUniversity of Montreal
6 · The paper itself

Abstract

backgroundPeople with human immunodeficiency virus (HIV) receiving antiretroviral therapy (ART) have increased risks of non-AIDS comorbidities. Growth differentiation factor 15 (GDF-15) is a mitokine released upon mitochondrial stress and is a validated aging biomarker. Herein, we assessed associations between plasma GDF-15 levels, inflammation, and HIV reservoir markers in ART-treated people with HIV (PWH).

methodsBlood samples were collected from 78 ART-naive, 140 ART-treated PWH (median ART duration, 15.6 years) and 83 uninfected control participants. GDF-15 and markers of inflammation were quantified in plasma by enzyme-linked immunosorbent assay (ELISA) and multiplex assays. Integrated HIV DNA levels were measured in isolated CD4 T cells by ultrasensitive quantitative Alu polymerase chain reaction. Intracellular GDF-15 production was assessed ex vivo by flow cytometry, and in supernatants by ELISA after in vitro stimulations.

resultsPlasma GDF-15 levels were higher in ART-treated PWH compared to ART-naive PWH or controls, independently of age. Ex vivo, GDF-15 was produced by classical, intermediate, and nonclassical monocytes, but absent in T cells, B cells, natural killer cells, and dendritic cells. Plasma and monocyte intracellular GDF-15 levels correlated strongly (r = 0.96, P = .002). Plasma GDF-15 levels did not correlate with the majority of inflammatory markers quantified in plasma. Conversely, plasma GDF-15 levels correlated with the validated non-AIDS inflammatory comorbidity marker suPAR (soluble urokinase plasminogen activator receptor; r = 0.59, P < .001), as well as with integrated HIV DNA levels in CD4+ T cells (r = 0.47, P < .01).

conclusionsPlasma levels of GDF-15, mainly produced by monocytes, were positively associated with HIV reservoir markers and coincided with increased level of suPAR, suggesting that HIV persistence is associated with increased mitochondrial stress and comorbidity risks in ART-treated PWH.

Indexed as

Anti-Retroviral AgentsGrowth Differentiation Factor 15HIV InfectionsInflammationAdultBiomarkersCD4-Positive T-LymphocytesDNA, ViralEnzyme-Linked Immunosorbent AssayFemaleHIV-1HumansMaleMiddle AgedViral LoadAnti-Retroviral AgentsBiomarkersDNA, ViralGDF15 protein, humanGrowth Differentiation Factor 15ARTCD4 T cellsGDF-15HIV reservoirsinflammation

Identifiers

PMID41966981
PMCPMC13537152

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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.