Kim Seung-Hyun, Ye Young-Min, Hur Gyu Young, Lee Soo-Keol, Sampson Anthony P, Lee Hyun-Young, Park Hae-Sim
Ajou University School of Medicine, Department of Allergy and Rheumatology, Yeongtonggu Wonchondong San-5, Suwon 443-721, Korea.
Pharmacogenomics. 2007 Sep;8(9):1143-50. doi: 10.2217/14622416.8.9.1143.
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.
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 (> or = 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.
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).
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.
白三烯受体拮抗剂(LTRA),如孟鲁司特,已被用作阿司匹林不耐受性哮喘(AIA)患者的一线治疗药物。本研究评估了韩国人群中89例AIA患者在长期管理中,白三烯受体拮抗剂的临床需求与花生四烯酸级联反应中ALOX5、LTC4S、COX - 2、CysLTR1和TBXA2R基因多态性之间的关联。
使用吸入性糖皮质激素和口服白三烯受体拮抗剂维持治疗,对哮喘控制状态进行1年监测,并根据维持哮喘控制1年每月所需的平均孟鲁司特剂量,将AIA患者分为三组:第一组(孟鲁司特≥200mg/月;n = 37),第二组(5 - 150mg/月;n = 25)和第三组(<5mg/月;n = 27)。采用单碱基延伸法测定花生四烯酸级联反应中的基因多态性。
我们发现三组之间CysLTR1启动子多态性-634C>T的基因型频率存在显著差异(第一组与第二组比较,p = 0.007;第一组与第三组比较,p = 0.017),而白三烯受体拮抗剂需求与其他基因的多态性之间无显著关联(-634C>T)。CysLTR1启动子多态性变异基因型(CT或TT)的患者比野生型基因型(CC)的患者表现出更高的表达水平。
这些发现表明,CysLTR1启动子多态性是预测AIA患者长期管理中白三烯受体拮抗剂需求的有用遗传标志物。