Evidence map›Paper›PMID 36672192›Full record

ArticleCells2023

Evaluation of Endocan as a Treatment for Acute Inflammatory Respiratory Failure.

Maxence Hureau, Lucie Portier, Méline Prin, Patricia de Nadai, Joanne Balsamelli, Anne Tsicopoulos, Daniel Mathieu, Philippe Lassalle, Bogdan Grigoriu, Alexandre Gaudet and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Maxence HureauUniv. de Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, CHU Lille, Surgical Critical Care, Department of Anesthesiology and Critical Care, F-59000 Lille, France.
Lucie PortierBiothelis, F-59000 Lille, France.
Méline PrinCentre Hospitalier de Valenciennes, Laboratoire d'Anatomopathologie, F-59300 Valenciennes, France.
Patricia de NadaiUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, F-59000 Lille, France.
Joanne BalsamelliUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, F-59000 Lille, France.
Anne TsicopoulosUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, CHU Lille, Service de Pneumologie et Immuno-Allergologie, Centre de Compétence pour les Maladies Pulmonaires Rares, F-59000 Lille, France.ORCID 0000-0002-1579-2763
Daniel MathieuUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, CHU Lille, Pôle de Médecine Intensive-Réanimation, F-59000 Lille, France.
Philippe LassalleBiothelis, F-59000 Lille, France.ORCID 0000-0001-6434-0344
Bogdan GrigoriuService des Soins Intensifs et Urgences Oncologiques, Institut Jules Bordet, Université Libre de Bruxelles (ULB), 1050 Brussels, Belgium.
Alexandre GaudetUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, CHU Lille, Pôle de Médecine Intensive-Réanimation, F-59000 Lille, France.
Nathalie De Freitas CairesBiothelis, F-59000 Lille, France.
Centre National de la Recherche Scientifique · FRCentre Hospitalier de Valenciennes · FRUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute respiratory distress syndrome (ARDS) is a life-threatening condition resulting from acute pulmonary inflammation. However, no specific treatment for ARDS has yet been developed. Previous findings suggest that lung injuries related to ARDS could be regulated by endocan (Esm-1). The aim of this study was to evaluate the potential efficiency of endocan in the treatment of ARDS.

methodsWe first compared the features of acute pulmonary inflammation and the severity of hypoxemia in a tracheal LPS-induced acute lung injury (ALI) model performed in knockout (

resultsIn our ALI model, we report higher alveolar leukocytes (

conclusionsEndocan appears to be an effective treatment in an ARDS-like model in C57Bl/6 mice.

Indexed as

Acute Lung InjuryPneumoniaRespiratory Distress SyndromeRespiratory InsufficiencyAnimalsLipopolysaccharidesMiceLipopolysaccharidesacute lung injuryacute respiratory distress syndromeendocanEsm-1respiratory failure

Identifiers

PMID36672192
PMCPMC9857156
OpenAlexW4313826415

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.