Marshall Nathaniel S, Yee Brendon J, Desai Anup V, Buchanan Peter R, Wong Keith K H, Crompton Renee, Melehan Kerri L, Zack Nadene, Rao Srinivas G, Gendreau R Michael, Kranzler Jay, Grunstein Ronald R
NHMRC Centre for Sleep Medicine, Woolcock Institute of Medical Research, University of Sydney, NSW Australia.
Sleep. 2008 Jun;31(6):824-31. doi: 10.1093/sleep/31.6.824.
Mirtazapine is an a2A antagonist and mixed 5-HT2/5-HT3 antagonist that has been proposed as a potential treatment for obstructive sleep apnea (OSA). A small, randomized, controlled trial has previously found an approximate halving in the severity of OSA with daily doses of 4.5 and 15 mg. We aimed to confirm and extend these findings in 2 randomized placebo-controlled, proof-of-concept trials.
Two randomized, double-blind, placebo-controlled trials of mirtazapine for OSA (apnea-hypopnea index 10-40/h). Study 1: 3-way crossover, dose-finding study testing the self-administration of mirtazapine (7.5, 15, 30, and/or 45 mg) or placebo 30 minutes prior to bedtime for 2 weeks at each dose. Twenty patients were randomly assigned to 1 of 6 different dose-sequence groups, with each patient exposed to a maximum of 3 doses. Study 2: 3-arm, randomized, parallel-group trial of mirtazapine at 15 mg or mirtazapine 15 mg + Compound CD0012 or placebo for 4 weeks in 65 patients with OSA.
Two patients withdrew from Study 1 after complaints of unacceptable lethargy. Fifteen patients were withdrawn from study 2, 7 after complaints of unacceptable lethargy or other side-effects. No measurement of sleep apnea improved due to mirtazapine in either study. Weight gain was significantly greater on mirtazapine than on placebo in both trials.
Mirtazapine did not improve sleep apnea in either trial. Mirtazapine caused weight gain, which may further worsen OSA. Therefore, mirtazapine is not recommended for the treatment of OSA.
米氮平是一种α2A拮抗剂及5-HT2/5-HT3混合拮抗剂,已被提议作为阻塞性睡眠呼吸暂停(OSA)的一种潜在治疗方法。之前一项小型随机对照试验发现,每日服用4.5毫克和15毫克剂量的米氮平可使OSA严重程度大致减半。我们旨在通过两项随机安慰剂对照的概念验证试验来证实并扩展这些发现。
两项关于米氮平治疗OSA(呼吸暂停低通气指数为10 - 40次/小时)的随机、双盲、安慰剂对照试验。研究1:三向交叉剂量探索研究,在睡前30分钟自行服用米氮平(7.5、15、30和/或45毫克)或安慰剂,每种剂量服用2周。20名患者被随机分配到6个不同剂量序列组中的1组,每位患者最多接受3种剂量。研究2:对65名OSA患者进行的三臂随机平行组试验,分别给予15毫克米氮平、15毫克米氮平 + 化合物CD0012或安慰剂,为期4周。
研究1中有两名患者因抱怨出现无法接受的嗜睡而退出。研究2中有15名患者退出,7名是因为抱怨出现无法接受的嗜睡或其他副作用。两项研究中,米氮平均未使睡眠呼吸暂停的测量指标得到改善。两项试验中,服用米氮平的患者体重增加显著高于服用安慰剂的患者。
两项试验中米氮平均未改善睡眠呼吸暂停。米氮平导致体重增加,这可能会使OSA进一步恶化。因此,不推荐使用米氮平治疗OSA。