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
相关论文
共 50 条
  • [31] Development of a Sublingual/Oral Formulation of Ketamine for Use in Neuropathic Pain Preliminary Findings from a Three-Way Randomized, Crossover Study
    Chong, Chui
    Schug, Stephan A.
    Page-Sharp, Madhu
    Jenkins, Barry
    Ilett, Kenneth F.
    CLINICAL DRUG INVESTIGATION, 2009, 29 (05) : 317 - 324
  • [32] A Randomized, Double-Blind, Placebo- and Positive-Controlled, Three-Way Crossover Study in Healthy Participants to Investigate the Effect of Savolitinib on the QTc Interval
    Sahota, Tarjinder
    Dota, Corina D.
    Vik, Torbjorn
    Yan, Weili
    Verheijen, Remy B.
    Walker, Stephen
    Li, Yan
    Goldwater, Ronald
    Ghiorghiu, Dana
    Mellemgaard, Anders
    Ahmed, Ghada F.
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2021, 10 (05): : 521 - 534
  • [33] Effect of low-dose rabeprazole and omeprazole on gastric acidity: results of a double blind, randomized, placebo-controlled, three-way crossover study in healthy subjects
    Des Varannes, SB
    Gharib, H
    Bicheler, V
    Bost, R
    Bonaz, B
    Stanescu, L
    Delchier, JC
    Bonnot-Marlier, S
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 20 (08) : 899 - 907
  • [34] THE PROTECTIVE EFFECT OF LOW-DOSE INHALED FENOTEROL AGAINST METHACHOLINE AND EXERCISE-INDUCED BRONCHOCONSTRICTION IN ASTHMA - A DOSE-RESPONSE STUDY
    MAGNUSSEN, H
    RABE, KF
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 90 (05) : 846 - 851
  • [35] Comparison of the effects of fasting morning, fasting evening and fed bedtime administration of tenatoprazole on intragastric pH in healthy volunteers: a randomized three-way crossover study
    Thomson, ABR
    Cohen, P
    Ficheux, H
    Fiorentini, P
    Domagala, F
    Homerin, M
    Taccoen, A
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2006, 23 (08) : 1179 - 1187
  • [36] Comparison of the effects of fasting morning, fasting evening, and fed bedtime administration of tenatoprazole on intragastric pH in healthy volunteers: A randomized three-way crossover study
    Thomson, Alan B. R.
    Cohen, Patrick
    Ficheux, Herve
    Domagala, Florence
    Homerin, Michel
    GASTROENTEROLOGY, 2006, 130 (04) : A177 - A177
  • [37] Pharmacokinetic properties of rosuvastatin after single-dose, oral administration in Chinese volunteers: A randomized, open-label, three-way crossover study
    Li, Yunxia
    Jiang, Xuehua
    Lan, Ke
    Zhang, Ruoqi
    Li, Xue
    Jiang, Qian
    CLINICAL THERAPEUTICS, 2007, 29 (10) : 2194 - 2203
  • [38] NALOXEGOL RESTORES CODEINE-INDUCED INHIBITION OF HIGH-AMPLITUDE PROPAGATING CONTRACTIONS IN A RANDOMIZED, THREE-WAY CROSSOVER COLONIC HIGH-RESOLUTION MANOMETRY STUDY IN HEALTHY VOLUNTEERS
    Pannemans, Jasper
    Demedts, Ingrid
    Geysen, Hannelore
    Vanuytsel, Tim
    Pauwels, Ans
    Tack, Jan F.
    GASTROENTEROLOGY, 2019, 156 (06) : S595 - S596
  • [40] HEMODYNAMIC AND PHARMACOKINETIC INTERACTIONS OF INTRANASAL BREMELANOTIDE AND ETHANOL IN A PHASE 1, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, THREE-PERIOD, THREE-WAY CROSSOVER STUDY
    Lucas, J.
    Clayton, A. H.
    DeRogatis, L. R.
    Jordan, R.
    JOURNAL OF SEXUAL MEDICINE, 2017, 14 (02): : E32 - E32