Bronchoprotective effect of vilanterol against methacholine-induced bronchoconstriction in mild asthmatics A randomized three-way crossover study

被引:3
|
作者
Westbury, Grace L. M. [1 ]
Blais, Christianne M. [2 ]
Davis, Beth E. [2 ]
Cockcroft, Donald W. [1 ,2 ]
机构
[1] Univ Saskatchewan, Coll Med, Div Respirol Crit Care & Sleep Med, Dept Physiol, Saskatoon, SK, Canada
[2] Univ Saskatchewan, Dept Med, Saskatoon, SK, Canada
关键词
ACTING BETA(2)-ADRENOCEPTOR AGONIST; INHALED METHACHOLINE; IN-VITRO; SALMETEROL; TOLERANCE; BRONCHODILATOR; RESPONSIVENESS; SALBUTAMOL; OLODATEROL; LUNG;
D O I
10.1016/j.anai.2018.07.005
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Ultra-long-acting beta 2 agonists (uLABA) are relatively new anti-asthma medications of which there are three different formulations currently available: olodaterol, indacaterol, and vilanterol. The first 2 formulations have been shown to exert bronchoprotective effects; they are able to prevent airway smooth muscle contraction on exposure to constricting stimuli. However, studies have found that these 2 drugs produce different degrees and durations of bronchoprotection against methacholine. Objective: The objective of this study was to investigate the degree of bronchoprotection provided by vilanterol against methacholine-induced bronchoconstriction. Methods: Fourteen patients with mild-to-moderate asthma (8 male; baseline percent predicted forced expiratory volume in 1 second [FEV1] > 65%; provocative concentration of methacholine causing a 20% reduction in FEV1 [PC20] <= 8 mg/mL) completed this randomized, double-blind, 3-way crossover study. Methacholine challenges were performed before treatment administration (placebo, 100 mu g fluticasone furoate, or 25 mu g vilanterol + 100 mu g fluticasone furoate) and at 0.5 and 24 hours posttreatment. Each treatment arm was separated by a minimum 7-day washout period. A combination therapy of vilanterol+fluticasone furoate was used, because vilanterol is not available as a monotherapy. Results: Significant bronchoprotection was evident after the combination treatment at both 0.5 and 24 hours with doubling dose shifts in methacholine PC20 of 2.0 (P=.0004) and 1.6 (P=.0001), respectively. Clinically significant bronchodilation was only recorded at 24 hours after combination treatment (P < .05). Conclusion: These findings suggest that vilanterol (in combination with fluticasone furoate) provides significant bronchoprotection against methacholine-induced bronchoconstriction for at least 24 hours in patients with mild-to-moderate asthma. Clinical Trial Registration: clinicaltrials.gov (NCT03315000). (C) 2018 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:328 / 332
页数:5
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