Busse William W, Pedersen Søren, Pauwels Romain A, Tan Wan C, Chen Yu-Zhi, Lamm Carl Johan, O'Byrne Paul M
Department of Medicine, University of Wisconsin School of Medicine and Public Health, J5/219 CSC, Box 2454, 600 Highland Ave, Madison, WI 53792, USA.
J Allergy Clin Immunol. 2008 May;121(5):1167-74. doi: 10.1016/j.jaci.2008.02.029. Epub 2008 Apr 11.
The Inhaled Steroid Treatment as Regular Therapy in Early Asthma (START) study enrolled 7241 patients aged 5 to 66 years with recent-onset, mild persistent asthma to assess early intervention with the inhaled corticosteroid budesonide on long-term asthma control.
The open-label phase of the START study was included to determine the effect on lung function and asthma control of adding budesonide to the reference group patients who had not initially received inhaled corticosteroids.
Patients were randomized to double-blind treatment with budesonide, 200 mug (those aged < 11 years) or 400 mug once daily, or placebo plus the usual asthma therapy for 3 years, after which all patients received 2 years of open-label treatment with budesonide once daily.
During the full 5-year study period, postbronchodilator FEV(1) percent predicted decreased, irrespective of randomized treatment during the double-blind phase, by an average of 2.22% (SE, 0.15%). However, patients with inhaled budesonide in the double-blind phase had a significantly lower risk (odds ratio, 0.61; P < .001) of a severe asthma-related event during the full 5-year study period than those in the reference group. Moreover, patients in the reference group used more additional asthma medications during both the open-label and double-blind phases.
In mild persistent asthma early intervention with inhaled budesonide was associated with improved asthma control and less additional asthma medication use.
早期哮喘吸入性类固醇常规治疗(START)研究纳入了7241例年龄在5至66岁的近期发病、轻度持续性哮喘患者,以评估吸入性皮质类固醇布地奈德早期干预对长期哮喘控制的效果。
START研究的开放标签阶段旨在确定在最初未接受吸入性皮质类固醇的参照组患者中加用布地奈德对肺功能和哮喘控制的影响。
患者被随机分为双盲治疗组,分别接受200微克(年龄<11岁者)或400微克布地奈德每日一次治疗,或接受安慰剂加常规哮喘治疗,为期3年,之后所有患者接受为期2年的布地奈德每日一次开放标签治疗。
在整个5年研究期间,无论双盲阶段的随机治疗情况如何,支气管扩张剂后第一秒用力呼气容积(FEV₁)预计值百分比平均下降2.22%(标准误,0.15%)。然而,在整个5年研究期间,双盲阶段接受吸入布地奈德治疗的患者发生严重哮喘相关事件的风险显著低于参照组(比值比,0.61;P<.001)。此外,参照组患者在开放标签阶段和双盲阶段使用的额外哮喘药物更多。
在轻度持续性哮喘中,吸入布地奈德早期干预与改善哮喘控制及减少额外哮喘药物使用有关。