The University of Southampton
University of Southampton Institutional Repository

Upper and lower airway nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and asthma

Upper and lower airway nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and asthma
Upper and lower airway nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and asthma
BACKGROUND: Patients with primary ciliary dyskinesia (PCD) have abnormal ciliary function and low nitric oxide levels. Nitric oxide (NO) biosynthesis is dependent on nitric oxide synthases (NOS). Cilia line the bronchial but not the alveolar epithelium. It has been hypothesised that NOS function relies on normal ciliary function and that in PCD bronchial but not alveolar NO might therefore be reduced. The aim of this study was to assess bronchial and alveolar NO levels primarily comparing healthy children to PCD and secondarily to cystic fibrosis (CF) and asthmatic children. METHODS: Multiple flow-rate fractional exhaled and nasal NO measurements were performed using a NIOX(®) Flex NO analyser (Aerocrine, Sweden) in children with PCD (n = 14), asthma (n = 18), CF (n = 12) and healthy controls (n = 18). Alveolar and bronchial NO levels were derived using a model of pulmonary NO exchange-dynamics. RESULTS: Both the bronchial and alveolar NO were significantly lower in PCD than healthy controls (mean (SD) 264 (209) picolitres/second (pl/s) vs. 720 (514) pl/s, p = 0.024 and 1.7 (0.8) parts per billion (ppb) vs. 3.5 (1.3) ppb, p = 0.001 respectively.) In asthmatics bronchial NO was found to be significantly higher than in healthy controls and in children with CF alveolar NO was significantly lower (2100 (1935) pl/s, p = 0.045 and 2.5 (1.2) ppb, p = 0.034 respectively.) CONCLUSION: Our findings do not support the hypothesis that NOS and ciliary function are coupled instead suggesting a more generalised mechanism for the low levels of NO seen in PCD. Our findings in CF and asthma corroborate evidence that these are diseases of the lung peripheries and bronchi respectively.
380-386
Walker, W.T.
58aae223-5b0e-4f34-9ee7-58bb68278c3a
Liew, A.
695839f5-30c3-4461-b990-f414147be84e
Harris, A.
13bbc5ce-730a-4918-b751-296ea3d60bb3
Cole, J.
2223ec60-016a-4802-9f1b-31e8198ab881
Lucas, J.S.
5cb3546c-87b2-4e59-af48-402076e25313
Walker, W.T.
58aae223-5b0e-4f34-9ee7-58bb68278c3a
Liew, A.
695839f5-30c3-4461-b990-f414147be84e
Harris, A.
13bbc5ce-730a-4918-b751-296ea3d60bb3
Cole, J.
2223ec60-016a-4802-9f1b-31e8198ab881
Lucas, J.S.
5cb3546c-87b2-4e59-af48-402076e25313

Walker, W.T., Liew, A., Harris, A., Cole, J. and Lucas, J.S. (2013) Upper and lower airway nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and asthma. Respiratory Medicine, 107 (3), 380-386. (doi:10.1016/j.rmed.2012.11.021). (PMID:23290188)

Record type: Article

Abstract

BACKGROUND: Patients with primary ciliary dyskinesia (PCD) have abnormal ciliary function and low nitric oxide levels. Nitric oxide (NO) biosynthesis is dependent on nitric oxide synthases (NOS). Cilia line the bronchial but not the alveolar epithelium. It has been hypothesised that NOS function relies on normal ciliary function and that in PCD bronchial but not alveolar NO might therefore be reduced. The aim of this study was to assess bronchial and alveolar NO levels primarily comparing healthy children to PCD and secondarily to cystic fibrosis (CF) and asthmatic children. METHODS: Multiple flow-rate fractional exhaled and nasal NO measurements were performed using a NIOX(®) Flex NO analyser (Aerocrine, Sweden) in children with PCD (n = 14), asthma (n = 18), CF (n = 12) and healthy controls (n = 18). Alveolar and bronchial NO levels were derived using a model of pulmonary NO exchange-dynamics. RESULTS: Both the bronchial and alveolar NO were significantly lower in PCD than healthy controls (mean (SD) 264 (209) picolitres/second (pl/s) vs. 720 (514) pl/s, p = 0.024 and 1.7 (0.8) parts per billion (ppb) vs. 3.5 (1.3) ppb, p = 0.001 respectively.) In asthmatics bronchial NO was found to be significantly higher than in healthy controls and in children with CF alveolar NO was significantly lower (2100 (1935) pl/s, p = 0.045 and 2.5 (1.2) ppb, p = 0.034 respectively.) CONCLUSION: Our findings do not support the hypothesis that NOS and ciliary function are coupled instead suggesting a more generalised mechanism for the low levels of NO seen in PCD. Our findings in CF and asthma corroborate evidence that these are diseases of the lung peripheries and bronchi respectively.

This record has no associated files available for download.

More information

Published date: 3 January 2013
Organisations: Faculty of Medicine

Identifiers

Local EPrints ID: 347047
URI: http://eprints.soton.ac.uk/id/eprint/347047
PURE UUID: bb6bbc6b-62bb-4cc9-aea7-33d84087311e
ORCID for J.S. Lucas: ORCID iD orcid.org/0000-0001-8701-9975

Catalogue record

Date deposited: 17 Jan 2013 12:28
Last modified: 15 Mar 2024 03:12

Export record

Altmetrics

Contributors

Author: W.T. Walker
Author: A. Liew
Author: A. Harris
Author: J. Cole
Author: J.S. Lucas ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×