β2-Adrenoceptor regulation and bronchodilator sensitivity after regular treatment with formoterol in subjects with stable asthma,☆☆,,★★

https://doi.org/10.1016/S0091-6749(98)70245-3Get rights and content

Abstract

Objective: We have previously found that β2-adrenoceptor downregulation and bronchodilator desensitization to albuterol occurred at 36 hours after stopping regular treatment with twice daily salmeterol. In this study we have evaluated these same effects with formoterol given once or twice daily on a regular basis. Methods: In a randomized, placebo-controlled, double-blind, double-dummy crossover study, 16 subjects with mild-to-moderate stable asthma (mean [SD] age, 32.5 [15.3] years; mean [SD] FEV1, 73.2 [12.1] percent predicted) receiving regular inhaled corticosteroid therapy received 1 week of treatment with formoterol dry powder (24 μg twice daily [8 <? check case >am<? check case >/8 <? check case >pm<? check case >]), formoterol (24 μg once daily [8 <? check case >pm<? check case >]), or identical placebo. Lymphocyte β2-adrenoceptor parameters and a dose-response curve to inhaled albuterol (200 to 1600 μg) were evaluated at 36 hours after the last dose of each treatment period. Results: There were no significant differences in the mean values for albuterol dose-response effects among the three treatment regimens. Comparison of maximal bronchodilator responses between treatments (mean and SEM as change from baseline) revealed no significant differences between treatments for FEV1 (0.47 L [0.06 L] for placebo vs 0.48 L [0.07 L] for 24 μg once daily formoterol vs 0.51 L [0.08 L] for 24 μg twice daily formoterol) or for forced expiratory flow, mid-expiratory phase (FEF25-75) (0.80 L/sec [0.12 L/sec] for placebo vs 0.80 L/sec [0.16 L/sec] for 24 μg once daily formoterol vs 0.89 L/sec [0.14 L/sec] for 24 μg twice daily formoterol). Formoterol also had no significant effect on mean lymphocyte β2-adrenoceptor density. However, in five of seven patients with the homozygous Gly-16 polymorphism, β2-adrenoceptor density was downregulated by twice daily formoterol, whereas only two such cases exhibited a reduction in maximal FEV1 response to albuterol. Conclusions: The results of this study showed that for patients taking inhaled corticosteroids, overall β2-adrenoceptor regulation and associated bronchodilator sensitivity to inhaled albuterol were unaltered at 36 hours after stopping regular treatment with formoterol. However, in a subset of patients who were Gly-16 homozygous, there was a tendency towards downregulation but not desensitization. Further studies in subjects with more severe asthma are required to assess the clinical relevance of these findings. (J Allergy Clin Immunol 1998;101:337-41.)

Section snippets

Patients

Sixteen asthmatic subjects (eight male and eight female) (mean [SD] age, 32.5 years [15.3 years]) who were all taking inhaled corticosteroids (mean [SD] dose 800 μg/day [664 μg/day]) were recruited to take part in the study. All the subjects were using inhaled short-acting β2-agonists on an as-required basis (<2 puffs/day) for relief of symptoms, five patients were using long-acting β2-agonists (three using salmeterol and two using formoterol), and three patients were also receiving oral

Results

All subjects completed the study, and no significant adverse effects were reported. Regular twice daily treatment with formoterol produced a significant (p < 0.05) improvement in the domiciliary morning and evening peak expiratory flow rates as compared with placebo. Morning peak expiratory flow rates were 395 L/min (27 L/min) for placebo, 424 L/min (30 L/min) for 24 μg once daily formoterol, and 431 L/min (30 L/min) for 24 μg twice daily formoterol. Evening peak expiratory flow rates were 420

Discussion

Our results in asthmatic patients showed that mean values for bronchodilator sensitivity to albuterol were not impaired at 36 hours after stopping regular treatment with 24 μg once or twice daily formoterol. Indeed, this was mirrored by effects on mean values for lymphocyte β2-adrenoceptor, which showed no evidence of downregulation (Bmax) or desensitization (Emax) at the same time point. We recently performed a similar study in healthy volunteers in which β2-adrenoceptor downregulation and

Cited by (0)

From athe Department of Clinical Pharmacology and Therapeutics and Respiratory Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee; and bthe Department of Medicine, Division of Therapeutics, University Hospital of Nottingham, Nottingham.

☆☆

Supported by a university grant, and Ian P. Hall is supported by the National Asthma Campaign.

Reprint requests: Brian J. Lipworth, MD, Department of Clinical Pharmacology and Therapeutics and Respiratory Medicine, Ninewells Hospital and medical School, University of Dundee, Dundee DD1 9SY, Scotland, United Kingdom.

★★

1/1/87717

View full text