Evidence map›Paper›PMID 28473708›Full record

ArticleScientific reports2017

Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease.

Kimberley C W Wang, Chrissie J Astell, Philip Wijesinghe, Alexander N Larcombe, Gavin J Pinniger, Graeme R Zosky, Brendan F Kennedy, Luke J Berry, David D Sampson, Alan L James and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 5 institutions in 2 countries.

Kimberley C W WangTelethon Kids Institute, The University of Western Australia, Subiaco, Western Australia, Australia. kimberley.wang@telethonkids.org.au.
Chrissie J AstellSchool of Anatomy, Physiology and Human Biology, The University of Western Australia, Perth, Western Australia, Australia.
Philip WijesingheOptical+Biomedical Engineering Laboratory, School of Electrical, Electronic & Computer Engineering, The University of Western Australia, Perth, Western Australia, Australia.
Alexander N LarcombeTelethon Kids Institute, The University of Western Australia, Subiaco, Western Australia, Australia.
Gavin J PinnigerSchool of Anatomy, Physiology and Human Biology, The University of Western Australia, Perth, Western Australia, Australia.
Graeme R ZoskyTelethon Kids Institute, The University of Western Australia, Subiaco, Western Australia, Australia.
Brendan F KennedyBRITElab, Harry Perkins Institute of Medical Research QEII Medical Centre, Crawley, Western Australia, Australia.
Luke J BerryTelethon Kids Institute, The University of Western Australia, Subiaco, Western Australia, Australia.
David D SampsonOptical+Biomedical Engineering Laboratory, School of Electrical, Electronic & Computer Engineering, The University of Western Australia, Perth, Western Australia, Australia.ORCID 0000-0001-6724-3873
Alan L JamesSir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Timothy D Le CrasCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Peter B NobleTelethon Kids Institute, The University of Western Australia, Subiaco, Western Australia, Australia.
The University of Western Australia · AUThe Kids Research Institute Australia · AUCincinnati Children's Hospital Medical Center · USSir Charles Gairdner Hospital · AUUniversity of Tasmania · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study tested the utility of optical coherence tomography (OCT)-based indentation to assess mechanical properties of respiratory tissues in disease. Using OCT-based indentation, the elastic modulus of mouse diaphragm was measured from changes in diaphragm thickness in response to an applied force provided by an indenter. We used a transgenic mouse model of chronic lung disease induced by the overexpression of transforming growth factor-alpha (TGF-α), established by the presence of pleural and peribronchial fibrosis and impaired lung mechanics determined by the forced oscillation technique and plethysmography. Diaphragm elastic modulus assessed by OCT-based indentation was reduced by TGF-α at both left and right lateral locations (p < 0.05). Diaphragm elastic modulus at left and right lateral locations were correlated within mice (r = 0.67, p < 0.01) suggesting that measurements were representative of tissue beyond the indenter field. Co-localised images of diaphragm after TGF-α overexpression revealed a layered fibrotic appearance. Maximum diaphragm force in conventional organ bath studies was also reduced by TGF-α overexpression (p < 0.01). Results show that OCT-based indentation provided clear delineation of diseased diaphragm, and together with organ bath assessment, provides new evidence suggesting that TGF-α overexpression produces impairment in diaphragm function and, therefore, an increase in the work of breathing in chronic lung disease.

Indexed as

Tomography, Optical CoherenceAnimalsBiomechanical PhenomenaDiaphragmDisease Models, AnimalDoxycyclineElastic ModulusFemaleFibrosisLung DiseasesMaleMice, TransgenicPleuraTransforming Growth Factor alphaDoxycyclineTransforming Growth Factor alpha

Identifiers

PMID28473708
PMCPMC5431417
OpenAlexW2607712533

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.