Evidence map›Paper›PMID 39998270›Full record

ArticleRespirology (Carlton, Vic.)2025

Functional Lung Imaging Identifies Peripheral Ventilation Changes in ꞵ-ENaC Mice.

Nicole Reyne, Ronan Smith, Patricia Cmielewski, Nina Eikelis, Kris Nilsen, Jennie Louise, Julia Duerr, Marcus A Mall, Mark Lawrence, David Parsons and 1 more

Abstract read
In one paragraph

Article in Respirology (Carlton, Vic.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

11 authors.

Nicole ReyneRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0002-3487-0827
Ronan SmithRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0002-5748-9295
Patricia CmielewskiRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Nina Eikelis4DMedical, Carlton, Victoria, Australia.ORCID 0000-0002-4001-1674
Kris Nilsen4DMedical, Carlton, Victoria, Australia.
Jennie LouiseBiostatistics Unit, South Australian Health and Medical Research Institute, Adelaide, Australia.
Julia DuerrDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Marcus A MallDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Mark LawrenceSCIREQ Scientific Respiratory Equipment Inc, Montreal, Quebec, Australia.
David ParsonsRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Martin DonnelleyRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.

Funding

Cystic Fibrosis Foundation DONNEL21GOGerman Federal Ministry of Education and Research 82DZL009B1German Research Foundation CRC 1449Medical Research Future Fund RFRHPSI000013
6 · The paper itself

Abstract

BACKGROUND AND

objectiveβ-ENaC-Tg mice serve as a relevant model of muco-obstructive lung disease and diffuse-type emphysema, with impaired mucociliary clearance, mucus obstruction, chronic airway inflammation, structural lung damage, and altered lung function. The aim of this study was to undertake a comprehensive analysis of lung function and mechanics of the adult β-ENaC-Tg model.

methodsAdult β-ENaC-Tg and wild-type littermates underwent X-ray velocimetry (XV) scans using a Permetium XV scanner (4DMedical, Melbourne, Australia). For comparative lung mechanics, lung function assessments were conducted with a flexiVent system (SCIREQ, Montreal, Canada).

resultsXV imaging demonstrated elevated ventilation defect percentage, mean specific ventilation, and ventilation heterogeneity in β-ENaC-Tg mice. Spatial analysis of ventilation maps indicated increased ventilation variability in the peripheral lung regions, as well as an increased proportion of under-ventilated areas. The flexiVent analysis indicated that compared to wild types, β-ENaC-Tg mice have a significantly more compliant lungs with increased inspiratory capacity, reduced tissue elastance, and increased hysteresivity (heterogeneity), suggesting loss of parenchymal integrity.

conclusionThis research highlights the utility of XV imaging in evaluating ventilation defects in the β-ENaC-Tg model and provides a comprehensive lung function analysis.

Indexed as

Epithelial Sodium ChannelsLungPulmonary EmphysemaPulmonary VentilationAnimalsDisease Models, AnimalMaleMiceMice, TransgenicRespiratory Function TestsRespiratory MechanicsEpithelial Sodium ChannelsScnn1b protein, mouseanimal modelscystic fibrosislung diseaselung functionmuco‐obstructivex‐ray velocimetry

Identifiers

PMID39998270
PMCPMC11965024

What OpenQuestion holds

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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.