Dahlén Sven-Erik, Malmström Kerstin, Nizankowska Ewa, Dahlén Barbro, Kuna Piotr, Kowalski Marek, Lumry William R, Picado César, Stevenson Donald D, Bousquet Jean, Pauwels Romain, Holgate Stephen T, Shahane Aditi, Zhang Ji, Reiss Theodore F, Szczeklik Andrew
Experimental Asthma and Allergy Research, The National Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Am J Respir Crit Care Med. 2002 Jan 1;165(1):9-14. doi: 10.1164/ajrccm.165.1.2010080.
Leukotriene antagonists block the proinflammatory actions of leukotrienes (LT) and have been introduced as new treatments for asthma. Conventional therapy with glucocorticosteroids does not inhibit the biosynthesis of leukotrienes. We therefore tested whether addition of the leukotriene receptor antagonist montelukast was of therapeutic benefit in a group of aspirin-intolerant patients with asthma of whom 90% already were treated with moderate to high doses of glucocorticosteroids. Under double-blind conditions, 80 aspirin-intolerant patients with asthma were randomized to receive 4 wk oral treatment of either 10 mg of montelukast or placebo once daily at bedtime. Pulmonary function was measured as forced expiratory volume in 1 s (FEV(1)) once a week in the clinic and daily as morning and evening peak expiratory flow rate (PEFR). Asthma symptoms and use of rescue bronchodilator were also recorded daily. Asthma specific quality of life (QoL) was assessed before and after the treatments. The group receiving montelukast showed a remarkable improvement of their asthma, whereas the group given placebo showed no change. Thus, from equal baseline values, the mean difference between the groups over the 4-wk treatment period was 10.2% for FEV(1) and 28.0 L for morning PEFR (p for both < 0.001). The improved pulmonary function in the group receiving montelukast occurred at the same time as 27% less bronchodilator was used (p < 0.05), and it was associated with fewer asthma symptoms than in the group given placebo, including 1.3 nights more of sleep per week and 54% fewer asthma exacerbations (p < 0.05). There was also an improvement in asthma-specific QoL (p < 0.05). The therapeutic response to montelukast was consistent across patients with different baseline characteristics and did not correlate with baseline urinary LTE(4). Addition of a leukotriene receptor antagonist such as montelukast improves asthma in aspirin-intolerant patients over and above what can be achieved by glucocorticosteroids.
白三烯拮抗剂可阻断白三烯(LT)的促炎作用,并已作为哮喘的新治疗方法被引入。糖皮质激素的传统疗法并不抑制白三烯的生物合成。因此,我们测试了在一组阿司匹林不耐受的哮喘患者中添加白三烯受体拮抗剂孟鲁司特是否具有治疗益处,这些患者中有90%已经接受了中高剂量糖皮质激素治疗。在双盲条件下,80名阿司匹林不耐受的哮喘患者被随机分为两组,一组每晚睡前口服10mg孟鲁司特,另一组口服安慰剂,为期4周。在诊所每周测量一次肺功能,以1秒用力呼气量(FEV(1))表示,每天早晚测量呼气峰值流速(PEFR)。每天还记录哮喘症状和急救支气管扩张剂的使用情况。在治疗前后评估哮喘特异性生活质量(QoL)。接受孟鲁司特治疗的组哮喘症状有显著改善,而接受安慰剂治疗的组则无变化。因此,从相同的基线值开始,在4周治疗期内,两组之间FEV(1)的平均差异为10.2%,早晨PEFR的平均差异为28.0L(两者p值均<0.001)。接受孟鲁司特治疗的组肺功能改善的同时,支气管扩张剂的使用减少了27%(p<0.05),与接受安慰剂治疗的组相比,哮喘症状更少,包括每周多睡1.3晚,哮喘发作减少54%(p<0.05)。哮喘特异性QoL也有改善(p<0.05)。孟鲁司特的治疗反应在具有不同基线特征的患者中是一致的,且与基线尿LTE(4)无关。添加孟鲁司特等白三烯受体拮抗剂可改善阿司匹林不耐受患者的哮喘,其效果优于糖皮质激素单独治疗所能达到的效果。