|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
* From the Departments of Pulmonology (Drs. Slats, van Klink, Bel, and Sterk) and Medical Decision Making (Dr. Sont), Leiden University Medical Center, Leiden, the Netherlands.
Correspondence to: Annelies M. Slats, Department of Pulmonology (C2-P-62), Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands; e-mail: a.m.slats{at}lumc.nl
Abstract
Background: Bronchodilation following deep inspiration is usually impaired in patients with asthma. This might be due to changes in airway mechanics in the presence of inflammation or structural changes within the airways. Although inhaled corticosteroid treatment has been shown to improve airway responses to deep inspiration in patients with asthma, airway inflammation can persist despite inhaled corticosteroid treatment, and thus could still influence the airway mechanics during deep breaths. We hypothesized that oral steroid treatment further optimizes deep inspiration-induced bronchodilation in clinically stable asthmatic patients who are receiving therapy with inhaled corticosteroids.
Methods: Twenty-four atopic patients with mild-to-moderate persistent asthma (FEV1, > 70% predicted; provocative concentration of methacholine causing a 20% fall in FEV1 [PC20], < 8 mg/mL), who were treated with 250 to 2,000 µg of beclomethasone-dipropionate or equivalent, participated in a parallel-design, double-blind study. Before and after treatment with 0.5 mg/kg/d prednisone or placebo for 14 days, a methacholine challenge was performed. Deep inspiration-induced bronchodilation was measured by the ratio of flow at 40% of FVC on the flow-volume curve after maximal inspiration/flow at 40% of FVC on the flow-volume curve after partial (60% of FVC) inspiration (M/P ratio).
Results: The M/P ratio significantly increased from a mean of 1.31 (range, 1.0 to 1.7) to 1.49 (range, 1.1 to 2.3) in the prednisone group. Interestingly, the improvement in the M/P ratio did not correlate with an accompanying significant increase in PC20 for methacholine (mean change, 1.02; SD doubling dose, 0.97) and a decrease in exhaled nitric oxide (mean change, 14 parts per billion [ppb]; SD, 33.4 ppb).
Conclusions: Systemic antiinflammatory treatment in addition to maintenance therapy with inhaled corticosteroids increases bronchodilation by deep inspiration in patients with mild-to-moderate persistent asthma. This suggests that residual inflammation impairs airway mechanics in asthma patients.
Key Words: airway inflammation bronchial hyperreactivity deep inspiration-induced bronchodilation glucocorticosteroid treatment nitric oxide prednisone
This article has been cited by other articles:
![]() |
D. W. Cockcroft Deep inhalation bronchodilation and oral corticosteroids in asthma. Chest, July 1, 2006; 130(1): 7 - 8. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |