Abstract

BackgroundMethacholine dose-response curves illustrate pharmacologic bronchoprotection against methacholine-induced airway hyperresponsiveness and can be used to quantitate changes in airway sensitivity (position), reactivity (slope), and maximal responsiveness following drug administration. Our objective was to determine the influence of single-dose glycopyrronium (long-acting muscarinic antagonist) and indacaterol (ultra-long acting β2 agonist), as monotherapy and in combination, on the methacholine dose-response curve of mild asthmatics and to compare these findings with a non-asthmatic control curve.MethodsThis was a randomized, double blind, double dummy, three-way crossover study. For asthmatic participants (n = 14), each treatment arm included a baseline methacholine challenge, drug administration, and repeat methacholine challenges at 1, 24, and 48 h. Non-asthmatic control participants (n = 15) underwent a single methacholine challenge and did not receive any study treatment. Methacholine dose-response curves were graphed as the percent fall in forced expiratory volume in 1 s (FEV1) for each methacholine concentration administered. Best-fit curves were then generated. Differences in airway reactivity were calculated through linear regression. Changes in airway sensitivity were assessed as the shift in the provocative concentration of methacholine causing a 20% fall in FEV1.ResultsCompared to baseline, all treatments significantly reduced airway sensitivity to methacholine at 1 h post-dose (indacaterol ~1.5 doubling concentrations; glycopyrronium ~5 doubling concentrations; combination ~5 doubling concentrations). Bronchoprotection at 24 and 48 h remained significant with glycopyrronium and combination therapy only. Airway reactivity was not influenced by indacaterol whereas glycopyrronium significantly reduced airway reactivity at all time-points (p = 0.003-0.027). The combination significantly decreased slope at 1 (p = 0.021) and 24 (p = 0.039) hours only. The non-asthmatic control and 1-h glycopyrronium curves are nearly identical. Only the non-asthmatic control and 1-h post-combination therapy curves appeared to generate a true response plateau (three data points within 5%), which occurred at a 14% fall in FEV1.ConclusionsMethacholine dose-response curves differentiate the bronchoprotective mechanisms triggered by different classes of asthma medications. Assessment of bronchoprotection using methacholine dose-response curves may be useful during clinical development of respiratory medications when performing superiority, equivalence, or non-inferiority trials.Trial registrationclinicaltrials.gov (NCT02953041). Retrospectively registered on October 24th 2016.

Highlights

  • Methacholine dose-response curves illustrate pharmacologic bronchoprotection against methacholineinduced airway hyperresponsiveness and can be used to quantitate changes in airway sensitivity, reactivity, and maximal responsiveness following drug administration

  • Methacholine dose-response curves differentiate the bronchoprotective mechanisms triggered by different classes of asthma medications

  • Assessment of bronchoprotection using methacholine dose-response curves may be useful during clinical development of respiratory medications when performing superiority, equivalence, or non-inferiority trials

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Summary

Introduction

Methacholine dose-response curves illustrate pharmacologic bronchoprotection against methacholineinduced airway hyperresponsiveness and can be used to quantitate changes in airway sensitivity (position), reactivity (slope), and maximal responsiveness following drug administration. The airway hyperresponsiveness component of asthma results from increases in both sensitivity and maximal responsiveness to bronchoconstrictors [1]. These effects can be visualized on a methacholine dose-response curve (MDRC); compared to healthy controls, the MDRC of asthmatics is shifted to the left (i.e. increased sensitivity to methacholine), has a steeper slope (i.e. increased airway reactivity), and either lacks or exhibits a raised plateau (i.e. excessive airway narrowing). Physiological factors that may increase airway sensitivity are epithelial damage or malfunction and increased inflammatory cell activity [1]. These factors may contribute to abnormal autonomic cholinergic activity in the airways [1]. An increased maximal airway response to methacholine could in turn result from excessive smooth muscle contractility, increased levels of intraluminal secretions and/or airway inflammation [1]

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