Evidence map›Paper›PMID 41820963›Full record

Observational studyCritical care (London, England)2026

Identification of a robust metabolic signature associated with hospital-acquired pneumonia and response to interferon-gamma treatment in critically ill patients.

Melanie Petrier, Debajyoti Sinha, Florian P Martin, Cecile Poulain, Delphine Flattres Duchaussoy, Athanasios Ziogas, Boris Novakovic, Laura Hurtado-Navarro, Anaísa V Ferreira, Joost H A Martens and 7 more

2 registry-linked trialsAbstract readObservational Study
In one paragraph

Observational study in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT02003196 completednot on this map

Effects of Viral Reactivation on Outcomes of Brain-injured Patients ( IBIS-VIRUS)

TypeobservationalSponsorNantes University HospitalRan2014 to 2020Enrolled375ConditionsBrain Injury
NCT04793568 phase2unknown statusnot on this map

Human Recombinant Interferon Gamma-1b for the Prevention of Hospital-acquired Pneumonia in Critically Ill Patients: a Double-blind, International, Phase 2, Randomized, Placebo-controlled Trial - the PREV-HAP Study

TypeinterventionalSponsorNantes University HospitalRan2021 to 2023Enrolled109ConditionsCritically Ill PatientsArmsRecombinant Interferon gamma 1b (IMUKIN®), Recombinant Interferon gamma 1b placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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.

Melanie PetrierCenter for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Debajyoti SinhaCenter for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Florian P MartinCenter for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Cecile PoulainCenter for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Delphine Flattres DuchaussoyNantes Université, CHU Nantes, Service d'Anesthesie Réanimation, Nantes, F-44000, France.
Athanasios ZiogasDepartment of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Boris NovakovicMurdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Australia.
Laura Hurtado-NavarroDepartment of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Anaísa V FerreiraDepartment of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Joost H A MartensDepartment of Molecular Biology, Faculty of Science, Radboud University Nijmegen, Nijmegen, the Netherlands.
Despoina KoulentiCritical Care Department, King's College Hospital NHS Foundation Trust, London, UK.
Laia Fernández-BaratCibeRes (Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, 06/06/0028), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Antoni TorresCibeRes (Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, 06/06/0028), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Emmanuel MontassierCenter for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Mihai G NeteaThe Biomedical Research Institute of Murcia (IMIB-Pascual Parrilla), Murcia, Spain.
Jeremie Poschmann *Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France.
Antoine Roquilly *Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes Université, Inserm, CHU Nantes, Nantes, F-44000, France. antoine.roquilly@univ-nantes.fr.

Funding

European Union's Horizon 2020 research and innovation program HAP2 - number 847782
6 · The paper itself

Abstract

aimOur objective was to increase our understanding of the effects of the time course of metabolic alterations on the risk of hospital-acquired pneumonia (HAP) and response to treatment in critically ill patients.

methodsWe first studied the blood metabolome at day 1, day 3-4 and day 6-7 of patients from a prospective, observational cohort of brain-injured patients in two French centres. We classified the metabolic response by unsupervised longitudinal consensus clustering. To evaluate the robustness of metabolic patterns, a Fast-and-Frugal Tree trained on the discovery cohort was applied to a replication dataset from the PREV-HAP randomised clinical trial testing interferon gamma-1b for the prevention of HAP in critically ill patients. The primary outcome was the association of metabolic response patterns with HAP.

findingsOf the 128 patients analysed (330 samples), 57 (45%) had developed HAP and 21 (16%) acute respiratory distress syndrome (ARDS). Based on metabolites involved in fatty acid metabolism, we identified three metabolic response patterns associated with the risks of HAP (24%, 60% and 78% of HAP, respectively) and ARDS (6%, 16% and 43%, respectively). In a replication dataset (315 samples from 105 patients), we found similarities regarding blood metabolite temporal courses and associations with HAP (18%, 28% and 40% of HAP, respectively). Moreover, the probability of being discharged alive from the ICU with interferon gamma-1b was decreased in patients with low-risk metabolic response patterns and increased in patients with high-risk metabolic response patterns.

conclusionsLongitudinal clustering classified metabolic response patterns into low-, moderate-, and high-risk groups for HAP and can help identify responders and non-responders to interferon gamma-1b after a single treatment injection.

trial registrationNumber clinicaltrial.gov NCT02003196 and NCT04793568.

Indexed as

Healthcare-Associated PneumoniaInterferon-gammaMetabolomeAgedCohort StudiesCritical IllnessFemaleFranceHumansMaleMiddle AgedProspective StudiesInterferon-gammaInterferon-gammaMetabolomePneumoniaPrecision medicine

Identifiers

PMID41820963
PMCPMC13094182

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.