Evidence map›Paper›PMID 42371909›Full record

Observational studyPloS one2026

Circulating biomarkers of bronchoalveolar injury help predict the need for mechanical ventilation in patients with moderate to severe COVID-19 pneumonia: A prospective cohort study.

Jérôme Allardet-Servent, Nathalie Hezard, Christel Pissier, Nathalie Bardin, Frédéric Cohen, Aurélie Dehaene, Rettinavelou Soundaravelou, Philippe Halfon, Anderson D Loundou, Marie-Christine Alessi and 1 more

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2026. 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

11 authors.

Jérôme Allardet-ServentDepartment of Critical Care, Hôpital Européen, Marseille, France.ORCID 0000-0002-6464-2382
Nathalie HezardDepartment of Hematology, Biogénopôle, Hôpital de la Timone, APHM, Marseille, France.
Christel PissierDepartment of Oncobiology, Hôpital Nord, APHM, Marseille, France.
Nathalie BardinC2VN, INSERM 1263, INRAE 1260, Aix Marseille University, Marseille, France.
Frédéric CohenDepartment of Radiology, Hôpital Européen, Marseille, France.
Aurélie DehaeneDepartment of Radiology, Hôpital Européen, Marseille, France.
Rettinavelou SoundaravelouDepartment of Critical Care, Hôpital Européen, Marseille, France.
Philippe HalfonDepartment of Infectious Disease, Hôpital Européen, Marseille, France.
Anderson D LoundouDepartment of Epidemiology, EA 3279-CEReSS, Aix Marseille University, Marseille, France.
Marie-Christine AlessiC2VN, INSERM 1263, INRAE 1260, Aix Marseille University, Marseille, France.
Pierre-Emmanuel MorangeC2VN, INSERM 1263, INRAE 1260, Aix Marseille University, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere respiratory failure is a major complication of SARS-CoV-2 infection, and the need for mechanical ventilation (MV) is associated with a worse outcome. Whether some soluble biomarkers of lung injury can help predict MV requirement remains unclear.

methodsThis prospective, observational, monocentric cohort study consecutively enrolled patients with laboratory-confirmed COVID-19 pneumonia within 48 h of hospital admission. The serum concentrations of five key bronchoalveolar epithelial and endothelial biomarkers were determined at Day 0, 7 and 14: Krebs von den Lungen-6 (KL-6); soluble receptor for advanced glycation end-products (sRAGE); club cell protein 16 (CC16); angiopoietin-2 (Ang-2); and soluble CD146 (sCD146). The respiratory severity of COVID-19 pneumonia was defined by the maximal level of respiratory support received during hospitalization: oxygen (by mask or nasal prong); high flow oxygen therapy (HFOT); and MV. End-points were the need for MV during hospitalization and the time to liberation from oxygen.

resultsFifty-four COVID-19 patients were enrolled; 23 (43%) required MV, 13 (24%) HFOT, and 18 (33%) oxygen. At inclusion, levels of KL-6, sRAGE, and CC16 were significantly higher in MV compared with non-MV patients (p < 0.05), with sRAGE showing the greatest difference (2.4-fold increase). In multivariate logistic regression, sRAGE (OR per 1000 pg/mL increase 1.316; 95% CI [1.040-1.667]; p = 0.022) and SpO2/FIO2 (OR 0.984; 95% CI [0.970-0.998]; p = 0.008) were identified as independent risk factors for MV. Furthermore, patients with an sRAGE ≥ 5449 pg/mL at inclusion had a lower probability of weaning from oxygen at Day 60 (HR 0.36; 95% CI [0.19-0.67]; p = 0.001). From Day 7 to Day 14, CC16 levels increased while sCD146 levels decreased in MV patients.

conclusionAmong five circulating biomarkers of bronchoalveolar injury, sRAGE showed the most favorable kinetic profile, rapidly increasing in MV patients. The early measurement of sRAGE and SpO2/FIO2 upon hospital admission may effectively identify COVID-19 patients at high risk of requiring MV and prolonged oxygen support.

Indexed as

BiomarkersCOVID-19Respiration, ArtificialAgedAngiopoietin-2CD146 AntigenFemaleHumansMaleMiddle AgedMucin-1Prospective StudiesReceptor for Advanced Glycation End ProductsSARS-CoV-2Severity of Illness IndexUteroglobinAngiopoietin-2BiomarkersCD146 AntigenMUC1 protein, humanMucin-1Receptor for Advanced Glycation End ProductsSCGB1A1 protein, humanUteroglobin

Identifiers

PMID42371909
PMCPMC13313340

What OpenQuestion holds

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LicenceCC BY
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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.