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Cross tolerance to salbutamol occurs independently of β2 adrenoceptor genotype-16 in asthmatic patients receiving regular formoterol or salmeterol
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  1. D K C Lee1,
  2. C M Jackson2,
  3. C E Bates1,
  4. B J Lipworth1
  1. 1Asthma and Allergy Research Group, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK
  2. 2Tayside Centre for General Practice, University of Dundee, Dundee DD1 9SY, UK
  1. Correspondence to:
    Professor B J Lipworth
    Asthma and Allergy Research Group, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK; b.j.lipworthdundee.ac.uk

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

  • This study received no support from the pharmaceutical industry and was funded from a departmental research grant from the University of Dundee.