Evidence map›Paper›PMID 40874168›Full record

ArticleERJ open research2025

Florence Jeny, Mohamed Nawfal Triba, Simon Chauveau, Dominique Valeyre, Sabrina Mokhtari, Hilario Nunes, Jean-Francois Bernaudin, Philippe Savarin

Erratum issuedAbstract read
In one paragraph

Article in ERJ open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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.

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. Metabolomic signaling in sarcoidosis pathogenesis.Current opinion in immunology · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Florence JenyHypoxia and Lung Laboratory, UMR INSERM 1272, Sorbonne Paris Nord University, SMBH Bobigny, Bobigny, France.ORCID https://orcid.org/0000-0003-4070-5569
Mohamed Nawfal TribaSorbonne Paris Nord University CB3S, UMR 7244, CNRS, Bobigny, France.
Simon ChauveauHypoxia and Lung Laboratory, UMR INSERM 1272, Sorbonne Paris Nord University, SMBH Bobigny, Bobigny, France.
Dominique ValeyreHypoxia and Lung Laboratory, UMR INSERM 1272, Sorbonne Paris Nord University, SMBH Bobigny, Bobigny, France.
Sabrina MokhtariSorbonne Paris Nord University CB3S, UMR 7244, CNRS, Bobigny, France.
Hilario NunesHypoxia and Lung Laboratory, UMR INSERM 1272, Sorbonne Paris Nord University, SMBH Bobigny, Bobigny, France.
Jean-Francois BernaudinHypoxia and Lung Laboratory, UMR INSERM 1272, Sorbonne Paris Nord University, SMBH Bobigny, Bobigny, France.
Philippe SavarinSorbonne Paris Nord University CB3S, UMR 7244, CNRS, Bobigny, France.ORCID https://orcid.org/0000-0003-1451-2376

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sarcoidosis is a systemic inflammatory immune disease characterised by noncaseating granulomas. Its course can vary from benign to very severe, requiring appropriate treatment. Few biomarkers are available to monitor the management of these patients and to identify those at risk of poor prognosis. Given the systemic nature of sarcoidosis, we hypothesised that the analysis of urine metabolites could provide valuable biomarkers for the management of severe disease. Methods: We conducted a comparative analysis of urine metabolomics in a consecutive cohort of 37 well-phenotyped patients, using Results: A urinary metabolomic signature predictive of severe pulmonary sarcoidosis was identified using a PLS model. We selected five metabolites with significant changes in samples from severe sarcoidosis defined by a composite physiologic index >40 compared to those from nonsevere sarcoidosis. These changes correspond to the decreased levels of taurine, hippurate, serine and creatinine and increased levels of 3-hydroxyisovalerate. This metabolite profile suggests an association with activated inflammatory pathways. Conclusions: This study shows that urinary NMR metabolites can discriminate samples between nonsevere and severe sarcoidosis. It suggests that urinary metabolomic studies in sarcoidosis may be particularly useful to identify potentially relevant biomarkers. However, further validation in a larger cohort of patients at different disease stages is warranted to confirm the relevance of these NMR biomarkers for follow-up.

Identifiers

PMID40874168
PMCPMC12378737

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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.