1 CIRUS, Centre for Sleep and Chronobiology, Woolcock Institute of Medical Research, University of Sydney, Sydney, Australia.
2 NeuroSleep, National Health and Medical Research Council Centre of Research Excellence, Sydney, Australia.
Am J Respir Crit Care Med. 2018 Oct 1;198(7):941-950. doi: 10.1164/rccm.201712-2439OC.
Patients with obstructive sleep apnea (OSA) unable to tolerate standard treatments have few alternatives. They may benefit from weight loss, but the major symptom of daytime performance impairment may remain during weight loss programs.
We hypothesized that wakefulness-promoter armodafinil would improve driving task performance over placebo in patients undergoing weight loss.
This was a placebo-controlled, double-blind, randomized trial of armodafinil versus placebo daily for 6 months in patients who were also randomized to one of two diets for 6 months with follow-up at 1 year in overweight, adult, patients with OSA who had rejected standard treatment and suffered daytime sleepiness.
Primary outcome was change in steering deviation in the final 30 minutes of a 90-minute afternoon driving task (AusED) at 6 months. Secondary outcomes were Epworth Sleepiness Scale, Functional Outcomes of Sleep Questionnaire, and fat mass measured by dual-emission X-ray absorptiometry. Armodafinil improved driving task performance over placebo at 3 months (12.9 cm; 95% confidence interval, 4.1-21.7; P = 0.004), but not the primary time point of 6 months (5.5 cm; 95% confidence interval, -3.3 to 14.3; P = 0.223). Patients on armodafinil lost 2.4 kg more fat than those on placebo at 6 months (95% confidence interval, 0.9-4.0; P = 0.002). Other secondary outcomes were not significantly improved.
Armodafinil did not improve driving task performance at the primary endpoint of 6 months. Armodafinil might be a useful adjunctive to weight loss in patients with OSA rejecting conventional treatments but this needs to be directly tested in a specifically designed, properly powered clinical trial. Clinical trial registered with Australian and New Zealand Clinical Trials Registry (ACTRN 12611000847910).
无法耐受标准治疗的阻塞性睡眠呼吸暂停(OSA)患者选择有限。他们可能受益于减肥,但在减肥计划期间,白天表现受损的主要症状可能仍然存在。
我们假设觉醒促进剂阿莫达非尼将改善减肥患者的驾驶任务表现,优于安慰剂。
这是一项安慰剂对照、双盲、随机临床试验,对拒绝标准治疗且白天嗜睡的超重成年 OSA 患者,在 6 个月内给予阿莫达非尼或安慰剂每日治疗,并随机分为两种饮食方案治疗 6 个月,在 1 年时进行随访。
主要结局是在 90 分钟下午驾驶任务的最后 30 分钟内转向偏差的变化,在 6 个月时评估。次要结局是 Epworth 睡眠量表、睡眠功能结局问卷和双能 X 射线吸收法测量的脂肪量。阿莫达非尼在 3 个月时改善了驾驶任务表现,优于安慰剂(12.9cm;95%置信区间,4.1-21.7;P=0.004),但在 6 个月时主要时间点没有改善(5.5cm;95%置信区间,-3.3 至 14.3;P=0.223)。在 6 个月时,服用阿莫达非尼的患者比服用安慰剂的患者多减去 2.4kg 脂肪(95%置信区间,0.9-4.0;P=0.002)。其他次要结局没有显著改善。
阿莫达非尼在 6 个月的主要终点时,没有改善驾驶任务表现。阿莫达非尼可能是拒绝传统治疗的 OSA 患者减肥的有用辅助手段,但这需要在专门设计的、适当的临床试验中进行直接测试。临床研究注册于澳大利亚和新西兰临床试验注册中心(ACTRN 12611000847910)。