Article Text
Abstract
Background: The development of tolerance following the use of long acting β2 agonists in asthmatic patients with either the homozygous arginine (Arg-16) or glycine (Gly-16) genotypes is poorly documented, especially in relation to the acute reliever response to salbutamol in constricted airways. A study was undertaken to evaluate the Arg-16 and Gly-16 genotypes for the acute salbutamol response following methacholine bronchial challenge between the first and last doses of formoterol (FM) and salmeterol (SM) combination inhalers.
Methods: Parallel groups of 10 matched homozygous Arg-16 and 10 homozygous Gly-16 patients completed a randomised, double blind, double dummy, crossover study. Following a 1 week washout period, patients received treatment for 2 weeks with either inhaled budesonide (BUD) 200 µg + FM 6 µg (two puffs twice daily) or inhaled fluticasone propionate (FP) 250 µg + SM 50 µg (one puff twice daily). After washouts and randomised treatments (1 hour after the first and last inhalation) a methacholine challenge was performed followed by salbutamol 200 µg, with recovery over 30 minutes (the primary outcome).
Results: Washout values for forced expiratory volume in 1 second (FEV1), methacholine hyperreactivity, and salbutamol recovery were similar for both treatments and genotypes. Pre-challenge FEV1 values for both genotypes did not differ significantly between the first and last doses of each treatment. Salbutamol recovery as mean (SE) area under the 30 minute time-response curve was significantly delayed (p<0.05) equally in both genotype and treatment groups. There were no differences in salbutamol recovery in either genotype or treatment group.
Conclusion: Acute salbutamol recovery in methacholine constricted airways was significantly delayed to a similar degree in both genotypes due to cross tolerance induced by FM or SM.
- BUD, budesonide
- FEV1, forced expiratory volume in 1 second
- FM, formoterol
- FP, fluticasone propionate
- PEF, peak expiratory flow
- SM, salmeterol
- asthma
- formoterol
- genotype
- salbutamol
- salmeterol
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Footnotes
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This study received no support from the pharmaceutical industry and was funded from a departmental research grant from the University of Dundee.