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Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics
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 L...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831603/ https://www.ncbi.nlm.nih.gov/pubmed/20224678 http://dx.doi.org/10.4168/aair.2010.2.1.48 |
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author | Park, Jong Sook Jang, An Soo Park, Sung Woo Lee, Young Mok Uh, Soo Taek Kim, Yong Hoon Cha, Ji Yean Park, Se Min Park, Choon-Sik |
author_facet | Park, Jong Sook Jang, An Soo Park, Sung Woo Lee, Young Mok Uh, Soo Taek Kim, Yong Hoon Cha, Ji Yean Park, Se Min Park, Choon-Sik |
author_sort | Park, Jong Sook |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2831603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease |
record_format | MEDLINE/PubMed |
spelling | pubmed-28316032010-03-11 Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics Park, Jong Sook Jang, An Soo Park, Sung Woo Lee, Young Mok Uh, Soo Taek Kim, Yong Hoon Cha, Ji Yean Park, Se Min Park, Choon-Sik Allergy Asthma Immunol Res Original Article 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. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2010-01 2009-12-30 /pmc/articles/PMC2831603/ /pubmed/20224678 http://dx.doi.org/10.4168/aair.2010.2.1.48 Text en Copyright © 2010 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Jong Sook Jang, An Soo Park, Sung Woo Lee, Young Mok Uh, Soo Taek Kim, Yong Hoon Cha, Ji Yean Park, Se Min Park, Choon-Sik Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title | Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title_full | Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title_fullStr | Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title_full_unstemmed | Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title_short | Protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
title_sort | protection of leukotriene receptor antagonist against aspirin-induced bronchospasm in asthmatics |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831603/ https://www.ncbi.nlm.nih.gov/pubmed/20224678 http://dx.doi.org/10.4168/aair.2010.2.1.48 |
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