Dissociation between exhaled nitric oxide and hyperresponsiveness in children with mild intermittent asthma

Citation
M. Silvestri et al., Dissociation between exhaled nitric oxide and hyperresponsiveness in children with mild intermittent asthma, THORAX, 55(6), 2000, pp. 484-488
Citations number
38
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
THORAX
ISSN journal
00406376 → ACNP
Volume
55
Issue
6
Year of publication
2000
Pages
484 - 488
Database
ISI
SICI code
0040-6376(200006)55:6<484:DBENOA>2.0.ZU;2-B
Abstract
Background-Bronchial hyperresponsiveness and airway inflammation are distin ctive features of asthma. Evaluation of nitric oxide (NO) levels in expired air have been proposed as a reliable method for assessing the airway infla mmatory events in asthmatic subjects. A study was undertaken to evaluate wh ether airway hyperresponsiveness is related to levels of exhaled NO. Methods-Thirty two steroid-naive atopic children with mild intermittent ast hma of mean (SD) age 11.8 (2.3) years and 28 age matched healthy controls w ere studied to investigate whether baseline lung function or airway hyperre sponsiveness is related to levels of exhaled NO. Airway responsiveness was assessed as the dose of methacholine causing a 20% decrease in forced expir atory volume in one second (FEV1) from control (PD20 methacholine) and exha led NO levels were measured by chemiluminescence analysis of exhaled air. Results-At baseline asthmatic children had significantly higher NO levels t han controls (mean difference 25.87 ppb (95% CI 18.91 to 32.83); p < 0.0001 ) but there were no significant differences in lung function parameters (fo rced vital capacity (FVC), FEV1 (% pred), and forced expiratory flows at 25 -75% of vital capacity (FEF25-75%)). In the asthmatic group exhaled NO leve ls were not significantly correlated with baseline lung function values or PD20 methacholine. Conclusions-These results suggest that levels of exhaled NO are not accurat e predictors of the degree of airway responsiveness to inhaled methacholine in children with mild intermittent asthma.