Evidence map›Paper›PMID 39284856›Full record

ArticleScientific reports2024

Assessment of respiratory mechanics and X-ray velocimetry functional imaging in two cystic fibrosis rat models.

Nicole Reyne, Ronan Smith, Patricia Cmielewski, Nina Eikelis, Mark Lawrence, Jennie Louise, Piraveen Pirakalathanan, David Parsons, Martin Donnelley

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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

9 authors.

Nicole ReyneRobinson Research Institute, University of Adelaide, Adelaide, SA, Australia. nikki.reyne@adelaide.edu.au.
Ronan SmithRobinson Research Institute, University of Adelaide, Adelaide, SA, Australia.
Patricia CmielewskiRobinson Research Institute, University of Adelaide, Adelaide, SA, Australia.
Nina Eikelis4DMedical, Melbourne, VIC, Australia.
Mark LawrenceSCIREQ Scientific Respiratory Equipment Inc, Montreal, QC, Canada.
Jennie LouiseBiostatistics Unit, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Piraveen Pirakalathanan4DMedical, Melbourne, VIC, Australia.
David ParsonsRobinson Research Institute, University of Adelaide, Adelaide, SA, Australia.
Martin DonnelleyRobinson Research Institute, University of Adelaide, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0002-5320-7756

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two cystic fibrosis (CF) rat models, one carrying the common Phe508del mutation and the other a nonsense cystic fibrosis transmembrane conductance regulator (CFTR) mutation (knockout) were previously characterised. Although relevant CFTR mRNA reductions were present in the lung, no overt CF lung disease was observed. This study used flexiVent lung mechanic assessment and regional ventilation assessment via X-ray velocimetry (XV) functional imaging to assess the lung phenotype in both models. To determine the sensitivity of XV regional ventilation imaging, the effect of a localised physical obstruction (delivery of agar beads to part of the lungs) on lung ventilation was examined. At baseline, Phe508del and knockout CF rats had a lower inspiratory capacity, total respiratory system compliance, and static compliance than wildtype rats. Following agar bead delivery all XV ventilation parameters were altered, with substantial increases in poorly ventilated regions and ventilation heterogeneity. XV ventilation maps accurately identified locations of bead-induced airflow changes. Despite unremarkable lung histopathology, this study indicated that CF rats display altered respiratory mechanics, with CF rats needing to exert additional effort to expand and deflate their lungs due to increased stiffness. This study demonstrated the utility of XV imaging providing spatial lung ventilation information.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDisease Models, AnimalLungRespiratory MechanicsAnimalsMaleRatsRats, Sprague-DawleyRheologyCystic Fibrosis Transmembrane Conductance RegulatorAnimal modelsCystic fibrosisflexiVentLungLung functionX-ray velocimetry

Identifiers

PMID39284856
PMCPMC11405763

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.