Effects of treatment with montelukast alone, budesonide/formoterol alone and a combination of both in cough variant asthma

Respir Res. 2022 Oct 10;23(1):279. doi: 10.1186/s12931-022-02114-6.

Abstract

Background: Whether cysteinyl-leukotriene receptor antagonists (LTRAs) have a similar antitussive effect to inhaled corticosteroids and long-acting β2-agonist (ICS/LABA), and that LTRA plus ICS/LABA is superior to LTRAs alone or ICS/LABA alone in treating cough variant asthma (CVA) remain unclear. This study aimed to investigate and compare the efficacy of montelukast alone, budesonide/formoterol alone and the combination of both in the treatment of CVA.

Methods: Ninety-nine CVA patients were assigned randomly in a 1:1:1 ratio to receive montelukast (M group: 10 mg, once daily), budesonide/formoterol (BF group: 160/4.5 μg, one puff, twice daily), or montelukast plus budesonide/formoterol (MBF group) for 8 weeks. The primary outcomes were changes in the cough visual analogue scale (VAS) score, daytime cough symptom score (CSS) and night-time CSS, and the secondary outcomes comprised changes in cough reflex sensitivity (CRS), the percentage of sputum eosinophils (sputum Eos%) and fractional exhaled nitric oxide (FeNO). CRS was presented with the lowest concentration of capsaicin that induced at least 5 coughs (C5). The repeated measure was used in data analysis.

Results: The median cough VAS score (median from 6.0 to 2.0 in the M group, 5.0 to 1.0 in the BF group and 6.0 to 1.0 in the MBF group, all p < 0.001), daytime CSS (all p < 0.01) and night-time CSS (all p < 0.001) decreased significantly in all three groups after treatment for 8 weeks. Meanwhile, the LogC5 and sputum Eos% improved significantly in all three groups after 8 weeks treatment (all p < 0.05). No significant differences were found in the changes of the VAS score, daytime and night-time CSSs, LogC5 and sputum Eos% among the three groups from baseline to week 8 (all p > 0.05). The BF and MBF groups also showed significant decreases in FeNO after 8 weeks treatment (p = 0.001 and p = 0.008, respectively), while no significant change was found in the M group (p = 0.457). Treatment with MBF for 8 weeks significantly improved the FEV1/FVC as well as the MMEF% pred and decreased the blood Eos% (all p < 0.05).

Conclusions: Montelukast alone, budesonide/formoterol alone and a combination of both were effective in improving cough symptom, decreasing cough reflex sensitivity and alleviating eosinophilic airway inflammation in patients with CVA, and the antitussive effect and anti-eosinophilic airway inflammation were similar. Trial registration ClinicalTrials.gov, number NCT01404013.

Keywords: Budesonide/formoterol; Cough; Cough variant asthma; Eosinophilic airway inflammation; Montelukast.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Acetates
  • Administration, Inhalation
  • Adrenal Cortex Hormones / therapeutic use
  • Antitussive Agents* / therapeutic use
  • Asthma* / diagnosis
  • Asthma* / drug therapy
  • Budesonide / therapeutic use
  • Budesonide, Formoterol Fumarate Drug Combination / therapeutic use
  • Capsaicin
  • Cough / diagnosis
  • Cough / drug therapy
  • Cyclopropanes
  • Formoterol Fumarate / therapeutic use
  • Humans
  • Inflammation
  • Leukotriene Antagonists
  • Quinolines
  • Sulfides

Substances

  • Acetates
  • Adrenal Cortex Hormones
  • Antitussive Agents
  • Budesonide, Formoterol Fumarate Drug Combination
  • Cyclopropanes
  • Leukotriene Antagonists
  • Quinolines
  • Sulfides
  • Budesonide
  • montelukast
  • Capsaicin
  • Formoterol Fumarate

Associated data

  • ClinicalTrials.gov/NCT01404013