Allergy Asthma Immunol Res.  2010 Jan;2(1):48-54. 10.4168/aair.2010.2.1.48.

Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics

Affiliations
  • 1Division of Respiratory and Allergy Medicine, Soonchunhyang University Hospital, College of Medicine, Bucheon, Korea. mdcspark@unitel.co.kr
  • 2Division of Respiratory and Allergy Medicine, Soonchunhyang University Hospital, College of Medicine, Seoul, Korea.
  • 3Division of Respiratory and Allergy Medicine, Soonchunhyang University Hospital, College of Medicine, Cheonan, Korea.
  • 4Genome Research Center for Allergy and Respiratory Disease, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.

Abstract

PURPOSE
Leukotriene receptor antagonists (LTRAs) are used to treat aspirin-intolerant asthma (AIA); however, the protective effects of long-term LTRA administration against aspirin-induced bronchospasm have not been evaluated.
OBJECTIVES
We investigated the efficacy of a 12-week treatment with a LTRA in protecting against aspirin-induced asthma in AIA patients.
METHODS
Fifty-two adult patients with AIA underwent an aspirin challenge test just before administration of montelukast (10 mg/day) and just after 12 weeks of treatment. The protective effect was assessed as the disappearance of aspirin-induced bronchospasm after 12 weeks of treatment. The results were compared according to the patients' clinical and physiological parameters.
RESULTS
The decline in FEV1 following aspirin challenge was significantly reduced from 28.6+/-1.9% to 10.2+/-1.7% (P=0.0001) after 12 weeks of montelukast treatment. However, 14 subjects (30%) still showed a positive response (>15% decline in FEV1) to aspirin challenge. Grouping the subjects into good and poor responders according to post-treatment responses revealed that the pretreatment aspirin-induced FEV1 decline was significantly greater in the poor responders and that the triggering dose of aspirin and the induction time for a positive response were lower and shorter, respectively, in the poor responders. Histories of aspirin hypersensitivity and sinusitis were more prevalent among the poor responders than among the good responders.
CONCLUSIONS
Twelve weeks of treatment with montelukast protected against aspirin-induced bronchospasm in 70% of the AIA cases. A poor response was associated with more severe aspirin-induced bronchospasms before treatment and a history of aspirin hypersensitivity or sinusitis. CLINICAL IMPLICATIONS: A severe response to aspirin challenge may be a predictor of poor responsiveness to leukotriene antagonist treatment.

Keyword

Asthma; leukotriene antagonists; aspirin; eosinophils

MeSH Terms

Acetates
Adult
Aspirin
Asthma
Asthma, Aspirin-Induced
Bronchial Spasm
Eosinophils
Humans
Hypersensitivity
Leukotriene Antagonists
Quinolines
Receptors, Leukotriene
Sinusitis
Acetates
Aspirin
Leukotriene Antagonists
Quinolines
Receptors, Leukotriene

Figure

  • Fig. 1 Change of % fall of FEV1 ratio following aspirin challenge after treatment with Montelukast. Aspirin induced - % fall in FEV1 were measured before and after treatment with daily 10 mg of Montelukast for 12 wk.


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