CysLTR1 promoter polymorphism and requirement for leukotriene receptor antagonist in aspirin-intolerant asthma patients

  • Kim S.-H.; 
  • Ye Y.-M.; 
  • Hur G.Y.; 
  • Lee S.-K.; 
  • Sampson A.P.; 
  • 외 2명
Citations

SCOPUS

51

초록

Objectives: Leukotriene receptor antagonists (LTRA), such as montelukast, have been used as a first-line treatment for patients with aspirin-intolerant asthma (AIA). This study evaluated associations between the clinical requirement for LTRA and genetic polymorphisms of the ALOX5, LTC4S, COX-2, CysLTR1 and TBXA2R genes in the arachidonic acid cascade in the long-term management of 89 AIA patients from a Korean population. Methods: Asthma control status was monitored for 1 year with maintenance medications of inhaled corticosteroid and oral LTRA, and AIA patients were classified into three groups according to the mean montelukast dose required per month to maintain asthma control for 1 year: group I (≥200 mg montelukast/month; n = 37), group II (5-150 mg/month; n = 25) and group III (<5 mg/month; n = 27). Genetic polymorphisms in the arachidonic acid cascade were determined using a single-base extension method. Results: We found that there was a significant difference in the genotype frequency of the CysLTR1 promoter polymorphism -634C > T among the three groups (p = 0.007 for group I vs group II, p = 0.017 for group I vs group III), while there were no significant associations between LTRA requirements and polymorphisms of the other genes. The patients with the variant genotype (CT or TT) of the -634C = T CysLTR1 promoter polymorphism showed a higher expression level than those with the common genotype (CC). Conclusion: These findings indicate that the CysLTR1 promoter polymorphism is a useful genetic marker for predicting LTRA requirements in the long-term management of AIA patients. © 2007 Future Medicine Ltd.

키워드

Aspirin-intolerant; Asthma; Cysteinyl leukotriene receptor 1; Genetic polymorphism; Leukotriene receptor antagonist; acetylsalicylic acid; arachidonate 5 lipoxygenase; arachidonic acid; beta 2 adrenergic receptor stimulating agent; budesonide; corticosteroid; cyclooxygenase 2; cysteinyl leukotriene receptor 1; immunoglobulin E; leukotriene C4 synthase; leukotriene receptor; leukotriene receptor blocking agent; methacholine; montelukast; thromboxane A2 receptor; unclassified drug; adult; article; aspirin sensitivity; asthma; bronchus hyperreactivity; controlled study; disease control; drug sensitivity; female; forced expiratory volume; gene expression; gene frequency; genetic association; genetic polymorphism; genetic variability; genotype; human; long term care; maintenance therapy; major clinical study; male; marker gene; patient compliance; pharmacogenetics; promoter region; rhinosinusitis; South Korea; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Asthma; Child; Drug Hypersensitivity; Forced Expiratory Volume; Humans; Korea; Leukotriene Antagonists; Membrane Proteins; Polymorphism, Genetic; Promoter Regions (Genetics); Receptors, Leukotriene
제목
CysLTR1 promoter polymorphism and requirement for leukotriene receptor antagonist in aspirin-intolerant asthma patients
저자
Kim S.-H.; Ye Y.-M.; Hur G.Y.; Lee S.-K.; Sampson A.P.; Lee H.-Y.; Park H.-S.
DOI
10.2217/14622416.8.9.1143
발행일
2007
유형
Article
저널명
Pharmacogenomics
권
8
호
9
페이지
1143 ~ 1150