首页> 外文期刊>British Journal of Clinical Pharmacology >A proof of concept study to evaluate putative benefits of montelukast in moderate persistent asthmatics.
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A proof of concept study to evaluate putative benefits of montelukast in moderate persistent asthmatics.

机译:概念验证研究评估孟鲁司特在中度持续性哮喘患者中的假定益处。

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AIMS: Whether chronic dosing with montelukast confers benefit in patients with moderate to severe asthma remains to be fully established. A proof of concept study was performed evaluating putative benefits with montelukast in moderate persistent asthmatics who were taken off inhaled corticosteroids (ICS) and switched to salmeterol. The latter was done to dissociate the effects of montelukast from ICS. METHODS: Twenty moderate to severe persistent asthmatics completed a randomized double-blind crossover study. Subjects received montelukast 10 mg daily or placebo for 2 weeks each. This was preceded by a 2-week run-in when ICS were discontinued and salmeterol started, and used on a regular basis throughout the study. Measurements were made after run-in and after both randomized treatments. RESULTS: There were no significant sequence effects for responses as to whether placebo or montelukast were given first or second. Methacholine PD20 values after run-in, first and second placebo were 63 micro g, 60 micro g and 64 micro g, respectively (corresponding to 2, 4 and 6 weeks of ICS washout, respectively). Lung function deteriorated pre vs post run-in, which was significant (P < 0.05) for FEF25-75 % predicted. Montelukast conferred significant (P < 0.05) improvements as change from post run-in compared with placebo in methacholine PD20, FEV1 % predicted, FEF25-75 % predicted, diurnal peak expiratory flow, symptoms and salbutamol use. For the primary outcome of methacholine PD20, this amounted to a 1.6-fold difference (95% CI 1.1, 2.5). CONCLUSIONS: In moderate persistent asthmatics switched from taking ICS to salmeterol alone, adding montelukast conferred significant benefits on all parameters of asthma control. Further studies are indicated to evaluate whether montelukast exhibits additive effects to ICS/long-acting beta2-adrenoceptor agonist combination inhalers upon clinically important outcomes.
机译:目的:孟鲁司特的长期给药是否能使中度至重度哮喘患者受益,尚待充分证实。进行了概念验证研究,以评估孟鲁司特在中度持续性哮喘中的潜在益处,这些哮喘患者已停用吸入皮质类固醇(ICS)并改用沙美特罗治疗。后者的作用是使孟鲁司特的作用与ICS分离。方法:20名中度至重度持续性哮喘患者完成了一项随机双盲交叉研究。受试者接受孟鲁司特每日10 mg或安慰剂,每人2周。在停药ICS并开始使用沙美特罗之前需要进行为期2周的磨合,并在整个研究过程中定期使用。在磨合后和两种随机治疗后进行测量。结果:安慰剂或孟鲁司特是先给予还是次要,对应答没有明显的序列影响。磨合,第一个和第二个安慰剂后的甲氧胆碱PD20值分别为63微克,60微克和64微克(分别对应于ICS洗脱的2、4和6周)。肺部功能恶化之前和之后磨合,这对于FEF25-75%的预测值是显着的(P <0.05)。与乙酰甲胆碱PD20中的安慰剂相比,孟鲁司特在磨合后的变化方面具有显着(P <0.05)改善,预计FEV1%,FEF25-75%,昼夜峰值呼气流量,症状和沙丁胺醇的使用。对于乙酰甲胆碱PD20的主要结局,这相差1.6倍(95%CI 1.1,2.5)。结论:在中度持续性哮喘患者中,从单纯服用ICS改为沙美特罗,加入孟鲁司特对哮喘控制的所有参数均具有显着益处。有进一步的研究表明,孟鲁司特在临床上重要的预后是否可对ICS /长效β2-肾上腺素受体激动剂联合吸入剂表现出加成作用。

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