Literature DB >> 24373575

Mucus removal is impaired in children with cystic fibrosis who have been infected by Pseudomonas aeruginosa.

Beth L Laube1, Gail Sharpless2, Jane Benson2, Kathryn A Carson2, Peter J Mogayzel2.   

Abstract

OBJECTIVE: To determine if mucus removal is impaired in children with cystic fibrosis (CF) who have been recently infected with Pseudomonas aeruginosa. STUDY
DESIGN: We compared mucociliary clearance (MCC), cough clearance (CC), lung morphology, and forced expiratory volume in 1 second (FEV1) in 7- to 14-year-old children with CF and mild lung disease (FEV1 ≥ 80%). Children were either P. aeruginosa negative (n = 8), or P. aeruginosa positive (P. aeruginosa obtained from at least 1 airway culture in the preceding 18 months) (n = 10). MCC and CC were quantified from gamma camera imaging of the right lung immediately after inhalation of (99m)technetium sulfur-colloid (time 0), over the next 60 minutes (average percent clearance over the first 60 minutes [AveMCC60]), 60-90 minutes (average percent clearance between 70 and 90 minutes [AveMCC/CC90]), and after 24 hours (percent clearance after 24 hours [MCC24hrs]). Children coughed 30 times between 60 and 90 minutes. Lung morphology was assessed by high resolution computed tomography (HRCT) scores of both lungs (total score) and of the right lung, using the Brody scale. Percent AveMCC60, AveMCC/CC90, MCC24hrs, FEV1, and HRCT scores were compared across the 2 groups using unpaired t tests. Associations were assessed using Spearman correlation.
RESULTS: There were no differences between the 2 groups in AveMCC60, MCC24hrs, mean HRCT total scores, right lung HRCT scores, or mean FEV1. AveMCC/CC90 was significantly decreased in children with P. aeruginosa compared with those without (16.2% ± 11.0% vs 28.6% ± 7.8%, respectively; P = .016). There was a significant negative correlation of AveMCC60 and AveMCC/CC90 with total lung HRCT score (all P < .05) but not with FEV1.
CONCLUSIONS: Infection with P. aeruginosa is associated with a significant slowing of MCC/CC in children with mild CF and may be a more sensitive indicator of the effects of P. aeruginosa than measurements of FEV1.
Copyright © 2014 Mosby, Inc. All rights reserved.

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Year:  2013        PMID: 24373575     DOI: 10.1016/j.jpeds.2013.11.031

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  7 in total

1.  Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

Authors:  Timothy E Corcoran; Alex S Huber; Michael M Myerburg; Daniel J Weiner; Landon W Locke; Ryan T Lacy; Lawrence Weber; Michael R Czachowski; Darragh J Johnston; Ashok Muthukrishnan; Alison T Lennox; Joseph M Pilewski
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2019-04-10       Impact factor: 2.849

2.  Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR.

Authors:  Scott H Donaldson; Beth L Laube; Timothy E Corcoran; Pradeep Bhambhvani; Kirby Zeman; Agathe Ceppe; Pamela L Zeitlin; Peter J Mogayzel; Michael Boyle; Landon W Locke; Michael M Myerburg; Joseph M Pilewski; Brian Flanagan; Steven M Rowe; William D Bennett
Journal:  JCI Insight       Date:  2018-12-20

Review 3.  Mucosal Immunity in Cystic Fibrosis.

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Journal:  J Immunol       Date:  2021-12-15       Impact factor: 5.426

4.  Putrescine reduces antibiotic-induced oxidative stress as a mechanism of modulation of antibiotic resistance in Burkholderia cenocepacia.

Authors:  Omar M El-Halfawy; Miguel A Valvano
Journal:  Antimicrob Agents Chemother       Date:  2014-05-12       Impact factor: 5.191

5.  Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung.

Authors:  Landon W Locke; Michael M Myerburg; Daniel J Weiner; Matthew R Markovetz; Robert S Parker; Ashok Muthukrishnan; Lawrence Weber; Michael R Czachowski; Ryan T Lacy; Joseph M Pilewski; Timothy E Corcoran
Journal:  Eur Respir J       Date:  2016-03-23       Impact factor: 16.671

6.  Changes in mucociliary clearance over time in children with cystic fibrosis.

Authors:  Beth L Laube; Kathryn A Carson; Christopher M Evans; Vanessa L Richardson; Gail Sharpless; Pamela L Zeitlin; Peter J Mogayzel
Journal:  Pediatr Pulmonol       Date:  2020-05-29

7.  Viscoelastic properties of Pseudomonas aeruginosa variant biofilms.

Authors:  Erin S Gloag; Guy K German; Paul Stoodley; Daniel J Wozniak
Journal:  Sci Rep       Date:  2018-06-26       Impact factor: 4.996

  7 in total

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