Evidence map›Paper›PMID 38902794›Full record

Trial reportBMC research notes2024

FDG-PET/CT-based respiration-gated lung segmentation and quantification of lung inflammation in COPD patients.

Ayse Dudu Altintas Dogan, Thomas Quist Christensen, Torben Tranborg Jensen, Claus Bogh Juhl, Ole Hilberg, Else-Marie Bladbjerg, Søren Hess

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC research notes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03466021 (Effects of GLP-1 Receptor Agonist Treatment on Pulmonary Function and Quality of Life in Obese Patients With Chronic Obstructive Pulmonary Disease.), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT03466021 phase4completednot on this map

Effects of GLP-1 Receptor Agonist Treatment on Pulmonary Function and Quality of Life in Obese Patients With Chronic Obstructive Pulmonary Disease.

TypeinterventionalSponsorClaus Bogh JuhlRan2018 to 2020Enrolled40ConditionsPulmonary Disease, Chronic ObstructiveArmsLiraglutide, Placebo
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
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

7 authors.

Ayse Dudu Altintas DoganDepartment of Medicine, Regional Hospital Horsens, Sundvej 30, 8700, Horsens, Denmark. ayse.dogan@rsyd.dk.ORCID http://orcid.org/0000-0001-6953-9969
Thomas Quist ChristensenDepartment of Radiology and Nuclear Medicine, Hospital South West Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark.
Torben Tranborg JensenDepartment of Medicine, Hospital South West Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark.
Claus Bogh JuhlDepartment of Medicine, Hospital South West Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark.
Ole HilbergDepartment of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Esbjerg, Denmark.
Else-Marie BladbjergDepartment of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Esbjerg, Denmark.
Søren HessDepartment of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Esbjerg, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objective and results descriptionThe study objective was to investigate the potential of quantitative measures of pulmonary inflammation by [18 F]Fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) as a surrogate marker of inflammation in COPD. Patients treated with anti-inflammatory Liraglutide were compared to placebo and correlated with inflammatory markers. 27 COPD-patients (14 receiving Liraglutide treatment and 13 receiving placebo) underwent 4D-respiratory-gated FDG-PET/CT before and after treatment. Two raters independently segmented the lungs from CT images and measured activity in whole lung, mean standard uptake values (SUVmean) corrected for lean-body-mass in the phase-matched PET images of the whole segmented lung volume, and total lesion glycolysis (TLG; SUVmean multiplied by volume). Inter-rater reliability was analyzed with Bland-Altman analysis and correlation plots. We found no differences in metabolic activity in the lungs between the two groups as a surrogate of pulmonary inflammation, and no changes in inflammation markers. The purpose of the research and brief summary of main findings. The degree of and changes in pulmonary inflammation in chronic obstructive pulmonary disease (COPD) may be difficult to ascertain. Measuring metabolic activity as a surrogate marker of inflammation by FDG-PET/CT may be useful, but data on its use in COPD including reproducibility is still limited, especially with respiration-gated technique, which should improve quantification in the lungs. We assessed several quantitative measures of metabolic activity and correlated them with inflammation markers, and we assessed reproducibility of the methods. We found no differences in metabolic activity between the two groups (before and after 40 weeks treatment with Liraglutide vs. placebo). Bland-Altman analysis showed good agreement between the two raters.

trial registrationThe study was conducted between February 2018 and March 2020 at the Department of Pulmonary Diseases at Hospital South West Jutland and Lillebaelt Hospital, Denmark, and registered from March 2018 at clinicaltrials.gov with trial registration number NCT03466021.

Indexed as

Fluorodeoxyglucose F18LungPositron Emission Tomography Computed TomographyPulmonary Disease, Chronic ObstructiveAgedFemaleHumansLiraglutideMaleMiddle AgedPneumoniaRadiopharmaceuticalsRespirationFluorodeoxyglucose F18LiraglutideRadiopharmaceuticalsCOPDFDG-PET/CTGLP-1 RAInflammationRespiration-gated

Identifiers

PMID38902794
PMCPMC11188287

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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.