Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Charlestown, MA.
Washington University School of Medicine, Department of Neurology, St. Louis, MO.
J Clin Sleep Med. 2014 Feb 15;10(2):143-53. doi: 10.5664/jcsm.3440.
To assess the effect of armodafinil on task-related prefrontal cortex activation using functional magnetic resonance imaging (fMRI) in patients with obstructive sleep apnea (OSA) and excessive sleepiness despite continuous positive airway pressure (CPAP) therapy.
This 2-week, multicenter, prospective, randomized, double-blind, placebo-controlled, parallel-group study was conducted at five neuroimaging sites and four collaborating clinical study centers in the United States. Patients were 40 right-handed or ambidextrous men and women aged between 18 and 60 years, with OSA and persistent sleepiness, as determined by multiple sleep latency and Epworth Sleepiness Scale scores, despite effective, stable use of CPAP. Treatment was randomized (1:1) to once-daily armodafinil 200 mg or placebo. The primary efficacy outcome was a change from baseline at week 2 in the volume of activation meeting the predefined threshold in the dorsolateral prefrontal cortex during a 2-back working memory task. The key secondary measure was the change in task response latency.
No significant differences were observed between treatment groups in the primary or key secondary outcomes. Armodafinil was generally well tolerated. The most common adverse events (occurring in more than one patient [5%]) were headache (19%), nasopharyngitis (14%), and diarrhea (10%).
Armodafinil did not improve fMRI-measured functional brain activation in CPAP-treated patients with OSA and excessive sleepiness.
Double-Blind, Placebo-Controlled, Functional Neuroimaging Study of Armodafinil (200 mg/Day) on Prefrontal Cortical Activation in Patients With Residual Excessive Sleepiness Associated With Obstructive Sleep Apnea/Hypopnea.
使用功能磁共振成像(fMRI)评估阿莫达非尼对阻塞性睡眠呼吸暂停(OSA)患者持续气道正压通气(CPAP)治疗后仍存在过度嗜睡的前额叶皮层激活的影响。
这是一项为期 2 周、多中心、前瞻性、随机、双盲、安慰剂对照、平行组研究,在美国的五个神经影像学站点和四个合作临床研究中心进行。患者为 40 名右利手或双手灵巧的 18 至 60 岁男女,患有 OSA 和持续嗜睡,通过多次睡眠潜伏期和 Epworth 嗜睡量表评分确定,尽管有效且稳定地使用 CPAP。治疗随机(1:1)分为每日一次阿莫达非尼 200mg 或安慰剂。主要疗效终点为 2 周时双侧背外侧前额叶皮层激活体积与基线相比的变化,该变化符合预设阈值。关键次要指标是任务反应时的变化。
治疗组在主要或关键次要结局方面无显著差异。阿莫达非尼总体耐受性良好。最常见的不良事件(发生于 1 名以上患者[5%])为头痛(19%)、鼻咽炎(14%)和腹泻(10%)。
阿莫达非尼不能改善 CPAP 治疗的 OSA 和过度嗜睡患者的 fMRI 测量的功能性大脑激活。
阿莫达非尼(200mg/天)对阻塞性睡眠呼吸暂停低通气综合征患者残留过度嗜睡相关前额叶皮层激活的双盲、安慰剂对照、功能神经影像学研究。