Edelman J M, Turpin J A, Bronsky E A, Grossman J, Kemp J P, Ghannam A F, DeLucca P T, Gormley G J, Pearlman D S
Merck & Co., Inc., West Point, Pennsylvania 19486, USA.
Ann Intern Med. 2000 Jan 18;132(2):97-104. doi: 10.7326/0003-4819-132-2-200001180-00002.
Montelukast, an oral, once-daily leukotriene receptor antagonist, provides protection against exercise-induced bronchoconstriction.
To evaluate the effect of 8 weeks of therapy with salmeterol aerosol or montelukast on exercise-induced bronchoconstriction in adults with asthma.
8-week multicenter, randomized, double-blind study.
17 asthma treatment centers in the United States.
191 adults with asthma who had documented exercise-induced bronchoconstriction.
Qualified patients were randomly assigned to double-blind treatment with montelukast (10 mg once in the evening) or salmeterol (50 microg [2 puffs] twice daily).
Changes in pre-exercise and postexercise challenge values; percentage inhibition in the maximal percentage decrease in FEV1; the area above the FEV1-time curve; and time to recovery of FEV1 at days 1 to 3, week 4, and week 8 of treatment.
By day 3, similar and statistically significant reductions in maximal percentage decrease in FEV1 were seen with both therapies. Sustained improvement occurred in the montelukast group at weeks 4 and 8; at these time points, the bronchoprotective effect of salmeterol decreased significantly. At week 8, the percentage inhibition in the maximal percentage decrease in FEV1 was 57.2% in the montelukast group and 33.0% in the salmeterol group (P = 0.002). By week 8, 67% of patients receiving montelukast and 46% of patients receiving salmeterol had a maximal percentage decrease in FEV1 of less than 20%.
The bronchoprotective effect of montelukast was maintained throughout 8 weeks of study. In contrast, significant loss of bronchoprotection at weeks 4 and 8 was seen with salmeterol. Long-term administration of montelukast provided consistent inhibition of exercise-induced bronchoconstriction at the end of the 8-week dosing interval without tolerance.
孟鲁司特是一种口服的每日一次的白三烯受体拮抗剂,可预防运动诱发的支气管收缩。
评估沙美特罗气雾剂或孟鲁司特治疗8周对成年哮喘患者运动诱发支气管收缩的影响。
为期8周的多中心、随机、双盲研究。
美国17个哮喘治疗中心。
191名有运动诱发支气管收缩记录的成年哮喘患者。
符合条件的患者被随机分配接受双盲治疗,分别使用孟鲁司特(每晚10毫克)或沙美特罗(50微克[2喷],每日两次)。
运动前和运动后激发值的变化;FEV1最大百分比下降的抑制百分比;FEV1-时间曲线以上的面积;以及治疗第1至3天、第4周和第8周FEV1恢复的时间。
到第3天,两种治疗方法在FEV1最大百分比下降方面均出现了相似且具有统计学意义的降低。孟鲁司特组在第4周和第8周持续改善;在这些时间点,沙美特罗的支气管保护作用显著下降。在第8周,孟鲁司特组FEV1最大百分比下降的抑制百分比为57.2%,沙美特罗组为33.0%(P = 0.002)。到第8周,接受孟鲁司特治疗的患者中有67%、接受沙美特罗治疗的患者中有46%的FEV1最大百分比下降小于20%。
在为期8周的研究中,孟鲁司特的支气管保护作用持续存在。相比之下,沙美特罗在第4周和第8周出现了显著的支气管保护作用丧失。长期服用孟鲁司特在8周给药间隔结束时能持续抑制运动诱发的支气管收缩,且无耐受性。