O'Connor Brian J, Löfdahl Claes-Göran, Balter Meyer, Szczeklik Andrew, Boulet Louis-Philippe, Cairns Charles B
King's College London School of Medicine, London, UK. brian.o'
Respir Med. 2007 Jun;101(6):1088-96. doi: 10.1016/j.rmed.2007.01.017. Epub 2007 Mar 13.
To assess the therapeutic effects of oral zileuton tablets combined with low-dose beclomethasone compared to doubling the dose of beclomethasone, in improving lung function and reducing asthma symptoms.
Randomized, active-control, double-blind, parallel, multi-center study of zileuton (400 or 600 mg QID)+200 microg beclomethasone dipropionate (BDP) BID versus placebo+BDP 400 microg BID in asthmatics with baseline FEV(1) percent predicted values between 40% and 80% following a single-blind ICS (BDP 200 microg BID) 2-week run-in. During the 3-month double-blind treatment period, assessments included safety, daytime and nighttime symptoms, acute asthma exacerbations, beta(2)-agonist use, AM and PM peak expiratory flow (PEF) and FEV(1).
The addition of a 5-lipoxygenase (5-LO) inhibitor added to a low-dose of BDP showed no significant difference in FEV(1) compared to doubling the dose of BDP. FEV(1) improved in all 3 treatment groups, with mean increases of 10% with zileuton 600 mg QID+BDP 200 microg BID, 12% with zileuton 400mg QID+BDP 200 microg BID, and 11% with BDP 400 microg BID by study end. Within each treatment group, there were significant improvements in asthma symptoms and AM and PM PEF compared to baseline. No significant differences were observed between groups with regards to salbutamol use, acute asthma exacerbations, the requirement for oral/parenteral corticosteroids and adverse clinical events.
The addition of a 5-LO inhibitor added to low-dose beclomethasone may be an alternative to higher-doses of ICS in patients unable to achieve sufficient asthma control on low-dose ICS therapy.
评估口服齐留通片联合低剂量倍氯米松与将倍氯米松剂量加倍相比,在改善肺功能和减轻哮喘症状方面的治疗效果。
一项随机、活性对照、双盲、平行、多中心研究,比较齐留通(400或600毫克每日四次)+200微克二丙酸倍氯米松(BDP)每日两次与安慰剂+400微克BDP每日两次对基线第一秒用力呼气容积(FEV₁)预测值在40%至80%之间的哮喘患者的疗效,患者在单盲吸入性糖皮质激素(BDP 200微克每日两次)为期2周的导入期后参与研究。在3个月的双盲治疗期内,评估内容包括安全性、白天和夜间症状、急性哮喘加重、β₂激动剂使用情况、上午和下午的呼气峰值流速(PEF)以及FEV₁。
与将BDP剂量加倍相比,在低剂量BDP基础上加用5-脂氧合酶(5-LO)抑制剂在FEV₁方面无显著差异。所有3个治疗组的FEV₁均有改善,到研究结束时,齐留通600毫克每日四次+BDP 200微克每日两次组平均增加10%,齐留通400毫克每日四次+BDP 200微克每日两次组平均增加12%,BDP 400微克每日两次组平均增加11%。在每个治疗组内,与基线相比,哮喘症状以及上午和下午的PEF均有显著改善。在沙丁胺醇使用、急性哮喘加重、口服/胃肠外糖皮质激素需求以及不良临床事件方面,各治疗组之间未观察到显著差异。
对于在低剂量吸入性糖皮质激素治疗下无法实现充分哮喘控制的患者,在低剂量倍氯米松基础上加用5-LO抑制剂可能是高剂量吸入性糖皮质激素的一种替代方案。