Evidence map›Paper›PMID 28449678›Full record

ArticleRespiratory research2017

[

Aurélien Justet, Astrid Laurent-Bellue, Gabriel Thabut, Arnaud Dieudonné, Marie-Pierre Debray, Raphael Borie, Michel Aubier, Rachida Lebtahi, Bruno Crestani

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 116 citations in OpenAlex.

  1. Prognosis of idiopathic pulmonary fibrosis without anti-fibrotic therapy: a systematic review.European respiratory review : an official journal of the European Respiratory Society · 2020
    Pooled it
  2. PulmonaryEuropean journal of nuclear medicine and molecular imaging · 2018
    Trial
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  9. Imaging technologies in experimental pulmonary fibrosis research: essential tool for enhanced translational relevance.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  10. [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
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  14. QuantitativeArthritis research & therapy · 2024
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  16. Respirology case reports · 2024
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  17. Review
  18. Biomarkers in idiopathic pulmonary fibrosis: Current insight and future direction.Chinese medical journal pulmonary and critical care medicine · 2024
    Article
  19. Article
  20. [Science advances · 2024
    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

9 authors at 6 institutions in 1 country.

Aurélien JustetAPHP, Hôpital Bichat, Service de Pneumologie A, DHU FIRE, Centre de compétence des maladies pulmonaires rares, 46 rue Henri Huchard, 75018, Paris, France. aurelienjustet@yahoo.fr.
Astrid Laurent-BellueAPHP, Hôpital Beaujon Service de Médecine nucléaire, Clichy, France.
Gabriel ThabutAPHP, Hôpital Bichat, Service de Pneumologie et de Transplantation Pulmonaire, DHU FIRE, Paris, France.
Arnaud DieudonnéAPHP, Hôpital Beaujon Service de Médecine nucléaire, Clichy, France.
Marie-Pierre DebrayAPHP Hôpital Bichat, Service de Radiologie, Paris, France.
Raphael BorieAPHP, Hôpital Bichat, Service de Pneumologie A, DHU FIRE, Centre de compétence des maladies pulmonaires rares, 46 rue Henri Huchard, 75018, Paris, France.
Michel AubierAPHP, Hôpital Bichat, Service de Pneumologie A, DHU FIRE, Centre de compétence des maladies pulmonaires rares, 46 rue Henri Huchard, 75018, Paris, France.
Rachida LebtahiAPHP, Hôpital Beaujon Service de Médecine nucléaire, Clichy, France.
Bruno CrestaniAPHP, Hôpital Bichat, Service de Pneumologie A, DHU FIRE, Centre de compétence des maladies pulmonaires rares, 46 rue Henri Huchard, 75018, Paris, France. bruno.crestani@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRHôpital Beaujon · FRUniversité Paris Cité · FRDélégation Paris 7 · FRHôpital Bichat-Claude-Bernard · FRSorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a devastating disease characterized by an unpredictable course. Prognostic markers and disease activity markers are needed. The purpose of this single-center retrospective study was to evaluate the prognostic value of lung fluorodeoxyglucose ([

methodsWe included 27 IPF patients (IPF group) and 15 patients with a gastrointestinal neuroendocrine tumor without thoracic involvement (control group). We quantified lung SUV mean and SUV max, MLV and TLG and assessed clinical data, high-resolution CT (HRCT) fibrosis and ground-glass score; lung function; gender, age, physiology (GAP) stage at inclusion and during follow-up; and survival.

resultsLung SUV mean and SUV max were higher in IPF patients than controls (p <0.00001). For patients with IPF, SUV mean, SUV max, MLV and TLG were correlated with severity of lung involvement as measured by a decline in forced vital capacity (FVC) and diffusing capacity of the lungs for carbon monoxide (DLCO) and increased GAP score. In a univariate and in a multivariate Cox proportional-hazards model, risk of death was increased although not significantly with high SUV mean. On univariate analysis, risk of death was significantly associated with high TLG and MLV, which disappeared after adjustment functional variables or GAP index. Increased MLV and TLG were independent predictors of death or disease progression during the 12 months after PET scan completion (for every 100-point increase in TLG, hazard ratio [HR]: 1.11 (95% CI 1.06; 1.36), p = 0.003; for every 100-point increase in MLV, HR: 1.20 (1.04; 1.19), p = 0.002). On multivariable analysis including TLG or MLV with age, FVC, and DLCO or GAP index, TLG and MLV remained associated with progression-free survival (HR: 1.1 [1.03; 1.22], p = 0.01; and 1.13 [1.0; 1.2], p = 0.005).

conclusionFDG lung uptake may be a marker of IPF severity and predict progression-free survival for patients with IPF.

Indexed as

Fluorodeoxyglucose F18ComorbidityDisease-Free SurvivalFranceHumansIdiopathic Pulmonary FibrosisIncidenceMiddle AgedPositron Emission Tomography Computed TomographyPrognosisRadiopharmaceuticalsReproducibility of ResultsRisk FactorsSensitivity and SpecificitySmokingSurvival RateFluorodeoxyglucose F18RadiopharmaceuticalsPET scanPrognosisPulmonary fibrosisTotal lesion glycolysis

Identifiers

PMID28449678
PMCPMC5408423
OpenAlexW2608293247

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.