Literature DB >> 28881106

Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography.

Wieying Kuo1,2, Thomas Soffers1, Eleni-Rosalina Andrinopoulou3, Tim Rosenow4, Sarath Ranganathan5,6,7, Lidija Turkovic4, Stephen M Stick4,8,9, Harm A W M Tiddens1,2.   

Abstract

OBJECTIVE: To evaluate lung disease progression using airway and artery (AA) dimensions on chest CT over 2-year interval in young CF patients longitudinally and compare to disease controls cross-sectionally.
METHODS: Retrospective analysis of pressure controlled end-inspiratory CTs, 12 routine baseline (CT1 ) and follow up (CT2 ) from AREST CF cohort; 12 disease controls with normal CT. All visible AA-pairs were measured perpendicular to the airway axis. Inner and outer airway diameters and wall (outer-inner radius) thickness were divided by adjacent arteries to compute Ain A-, Aout A-, and AWT A-ratios, respectively. Differences between CF and control data were assessed using mixed effects models predicting AA-ratios per segmental generation (SG). Power calculations were performed with 80% power and ɑ = 0.05.
RESULTS: CF, median age CT1 2 years; CT2 3.9 years, 5 males. Controls, median age 2.9 years, 10 males. Total of 4798 AA-pairs measured. Cross-sectionally: Ain A-ratio showed no difference between controls and CF CT1 or CT2 . Aout A-ratio was significantly higher in CF CT1 (SG 2-4) and CT2 (SG 2-5) compared to controls. AWT A-ratio was increased for CF CT1 (SG 1-5) and CT2 (SG 2-6) compared to controls. CF longitudinally: Ain A-ratio was significantly higher at CT2 compared to CT1 . Increase in Aout A-ratio at CT2 compared to CT1 was visible in SG ≥4. Sample sizes of 21 and 58 would be necessary for 50% and 30% Aout A-ratio reductions, respectively, between CF CT2 and controls.
CONCLUSION: AA-ratio differences were present in young CF patients relative to disease controls. Aout A-ratio as an objective parameter for bronchiectasis could reduce sample sizes for clinical trials.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  biomarkers; bronchiectasis; cystic fibrosis; imaging

Mesh:

Year:  2017        PMID: 28881106     DOI: 10.1002/ppul.23787

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  6 in total

Review 1.  Novel imaging techniques for cystic fibrosis lung disease.

Authors:  Jennifer L Goralski; Neil J Stewart; Jason C Woods
Journal:  Pediatr Pulmonol       Date:  2021-02

2.  Lung inflammation and simulated airway resistance in infants with cystic fibrosis.

Authors:  Emily M DeBoer; Julia S Kimbell; Kaci Pickett; Joseph E Hatch; Kathryn Akers; John Brinton; Graham L Hall; Louise King; Fiona Ramanauskas; Tim Rosenow; Stephen M Stick; Harm A Tiddens; Thomas W Ferkol; Sarath C Ranganathan; Stephanie D Davis
Journal:  Respir Physiol Neurobiol       Date:  2021-06-19       Impact factor: 1.931

3.  Assessment of early lung disease in young children with CF: A comparison between pressure-controlled and free-breathing chest computed tomography.

Authors:  Merel C J Oudraad; Wieying Kuo; Tim Rosenow; Eleni-Rosalina Andrinopoulou; Stephen M Stick; Harm A W M Tiddens
Journal:  Pediatr Pulmonol       Date:  2020-03-02

4.  Airway disease on chest computed tomography of preschool children with cystic fibrosis is associated with school-age bronchiectasis.

Authors:  Nynke R Bouma; Hettie M Janssens; Eleni-Rosalina Andrinopoulou; Harm A W M Tiddens
Journal:  Pediatr Pulmonol       Date:  2019-09-09

5.  Chest computed tomography outcomes in a randomized clinical trial in cystic fibrosis: Lessons learned from the first ataluren phase 3 study.

Authors:  Harm A W M Tiddens; Eleni-Rosalina Andrinopoulou; Joe McIntosh; J Stuart Elborn; Eitan Kerem; Nynke Bouma; Jochem Bosch; Mariette Kemner-van de Corput
Journal:  PLoS One       Date:  2020-11-03       Impact factor: 3.240

6.  Functional respiratory imaging in relation to classical outcome measures in cystic fibrosis: a cross-sectional study.

Authors:  Eline Lauwers; Annemiek Snoeckx; Kris Ides; Kim Van Hoorenbeeck; Maarten Lanclus; Wilfried De Backer; Jan De Backer; Stijn Verhulst
Journal:  BMC Pulm Med       Date:  2021-08-04       Impact factor: 3.317

  6 in total

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