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Inhibition of the early asthmatic response to inhaled allergen by the 5-lipoxygenase activating protein inhibitor GSK2190915: a dose–response study

机译:5-脂氧合酶激活蛋白抑制剂GSK2190915抑制哮喘对吸入性变应原的早期哮喘反应:一项剂量反应研究

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Background: GSK2190915, a 5-lipoxygenase activating protein inhibitor, inhibits the production of cysteinyl leukotrienes and leukotriene B4 and 5-oxo-6,8,11,14-eicosatetraenoic acid. We have previously reported that GSK2190915 100 mg daily inhibits early and late asthmatic responses to inhaled allergen; the effects of lower doses have not been reported. This study assessed the dose–response effects of GSK2190915 10 mg and 50 mg on the early asthmatic response (EAR) to inhaled allergen.Methods: Nineteen subjects with mild asthma and an EAR were enrolled in a randomized, double-blind, three-way crossover study of GSK2190915 10 mg, 50 mg, and placebo orally once-daily for 3 days. Allergen challenge was performed 2 hours after the third dose.Results: Compared with placebo, GSK2190915 10 mg and 50 mg caused significant, dose-dependent attenuation of the minimum forced expiratory volume at 1 second (FEV1) absolute change from baseline; mean treatment differences were 0.21 L (95% confidence interval [CI] 0.04 L, 0.38 L) and 0.41 L (95% CI 0.24 L, 0.58 L), respectively. GSK2190915 50 mg was more effective than 10 mg; mean difference between treatments was 0.20 L, (95% CI 0.03 L, 0.36 L). Compared with placebo, GSK2190915 50 mg, but not 10 mg, significantly inhibited the weighted mean FEV1 absolute change from baseline.Conclusion: GSK2190915 50 mg attenuated the EAR similarly to GSK2190915 100 mg in our previous study, suggesting 50 mg is at the top of the dose–response curve. GSK2190915 10 mg is a suboptimal dose. The EAR can be used to assess the therapeutic dose of a new treatment for asthma.
机译:背景:GSK2190915,一种5-脂氧合酶激活蛋白抑制剂,可抑制半胱氨酰白三烯和白三烯B4和5-oxo-6,8,11,14-二十碳四烯酸的产生。我们以前曾报道过,每天100 mg GSK2190915会抑制早期和晚期哮喘对吸入性变应原的反应。尚未报道较低剂量的作用。这项研究评估了10 mg和50 mg GSK2190915对吸入性变应原的早期哮喘反应(EAR)的剂量反应。方法:对19名轻度哮喘和EAR患者进行了随机,双盲,三向研究每天一次口服10毫克,50毫克和安慰剂的GSK2190915的交叉研究,持续3天。结果:与安慰剂相比,10 mg和50 mg GSK2190915与安慰剂相比,在1秒钟时的最小强制呼气量(FEV1)与基线相比发生了剂量依赖性的显着衰减;平均治疗差异分别为0.21 L(95%置信区间[CI] 0.04 L,0.38 L)和0.41 L(95%CI 0.24 L,0.58 L)。 GSK2190915 50 mg比10 mg更有效;处理之间的平均差为0.20 L(95%CI 0.03 L,0.36 L)。与安慰剂相比,GSK2190915 50 mg(而非10 mg)显着抑制了FEV1加权平均绝对值相对于基线的变化。结论:GSK2190915 50 mg对EAR的衰减与GSK2190915 100 mg在我们先前的研究中相似,表明50 mg位于最上方剂量反应曲线。 GSK2190915 10 mg为次佳剂量。 EAR可用于评估哮喘新疗法的治疗剂量。

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