Flinders Health and Medical Research Institute/Adelaide Institute for Sleep Health, Flinders University, Bedford Park, South Australia, Australia.
Neuroscience Research Australia (NeuRA), University of New South Wales (UNSW), Randwick, Sydney, New South Wales, Australia.
J Clin Sleep Med. 2023 Jan 1;19(1):85-96. doi: 10.5664/jcsm.10256.
Recent findings indicate that noradrenergic and muscarinic processes are crucial for pharyngeal muscle control during sleep. However, to date, reductions in obstructive sleep apnea (OSA) severity have only been detected when noradrenergic agents are combined with an antimuscarinic. Accordingly, this study aimed to determine if reboxetine alone and combined with oxybutynin reduces OSA severity. The pathophysiological mechanisms underpinning the effects of these agents were also investigated via endotyping analysis.
Sixteen people (6 women) with OSA completed 3 polysomnograms (∼1-week washout) according to a double-blind, placebo-controlled, three-way crossover design across 2 sites. Single doses of 4 mg reboxetine, placebo, or 4 mg reboxetine + 5 mg oxybutynin were administered before sleep (order randomized).
Reboxetine reduced the apnea-hypopnea index (primary outcome) by 5.4 (95% confidence interval -10.4 to -0.3) events/h, = .03 (-24 ± 27% in men; -0.7 ± 32% in women). Oxybutynin did not cause additional reductions in apnea-hypopnea index. Reboxetine alone reduced the 4% oxygen desaturation index by (mean ± standard deviation) 5.2 ± 7.2 events/h and reboxetine+oxybutynin by 5.1 ± 10.6 events/h vs placebo, = .02. Nadir oxygen saturation also increased by 7 ± 11% with reboxetine and 5 ± 9% with reboxetine+oxybutynin vs placebo, = .01. Mechanistically, reboxetine and reboxetine+oxybutynin improved pharyngeal collapsibility and respiratory control (loop gain). Larger reductions in apnea-hypopnea index with reboxetine in men were associated with higher baseline loop gain.
These findings show the first evidence that reboxetine alone reduces OSA severity. The data provide novel insight into the role of norepinephrine reuptake inhibitors on upper airway stability during sleep and are important to inform future pharmacotherapy development for OSA.
Registry: Australian New Zealand Clinical Trials Registry; Name: Reboxetine and Combination Therapy with AD128 in Sleep Apnoea Trial: A Double-Blind, 3-Way Cross-Over Study; URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=374614&isReview=true; Identifier: ACTRN12620000662965.
Altree TJ, Aishah A, Loffler KA, Grunstein RR, Eckert DJ. The norepinephrine reuptake inhibitor reboxetine alone reduces obstructive sleep apnea severity: a double-blind, placebo-controlled, randomized crossover trial. . 2023;19(1):85-96.
最近的研究结果表明,去甲肾上腺素能和毒蕈碱能过程对于睡眠期间咽肌的控制至关重要。然而,迄今为止,只有当使用去甲肾上腺素能药物与抗毒蕈碱药物联合使用时,才检测到阻塞性睡眠呼吸暂停(OSA)严重程度的降低。因此,本研究旨在确定单独使用瑞波西汀和与奥昔布宁联合使用是否可以降低 OSA 的严重程度。还通过表型分析研究了这些药物作用的病理生理机制。
16 名 OSA 患者(6 名女性)在两个地点根据双盲、安慰剂对照、三向交叉设计完成了 3 次多导睡眠图(约 1 周洗脱期)。在睡前给予 4mg 瑞波西汀、安慰剂或 4mg 瑞波西汀+5mg 奥昔布宁的单剂量(随机排序)。
瑞波西汀降低了呼吸暂停低通气指数(主要结局)5.4(95%置信区间 -10.4 至 -0.3)次/小时,=0.03(男性中 -24±27%;女性中-0.7±32%)。奥昔布宁没有导致呼吸暂停低通气指数的额外降低。单独使用瑞波西汀可将 4%氧减饱和度指数降低(平均值±标准差)5.2±7.2 次/小时,瑞波西汀+奥昔布宁降低 5.1±10.6 次/小时,与安慰剂相比,=0.02。最低氧饱和度也增加了 7±11%,瑞波西汀增加了 5±9%,与安慰剂相比,=0.01。从机制上讲,瑞波西汀和瑞波西汀+奥昔布宁改善了咽腔塌陷和呼吸控制(环路增益)。男性中瑞波西汀治疗后呼吸暂停低通气指数的较大降低与较高的基线环路增益相关。
这些发现首次表明,单独使用瑞波西汀可降低 OSA 的严重程度。这些数据提供了关于去甲肾上腺素再摄取抑制剂在睡眠期间对上气道稳定性影响的新见解,对于为 OSA 开发未来的药物治疗具有重要意义。
澳大利亚新西兰临床试验注册处;名称:瑞波西汀和 AD128 在睡眠呼吸暂停中的联合治疗试验:双盲、三向交叉研究;网址:https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=374614&isReview=true;标识符:ACTRN12620000662965。
Altree TJ、Aishah A、Loffler KA、Grunstein RR、Eckert DJ。去甲肾上腺素再摄取抑制剂瑞波西汀单独使用可降低阻塞性睡眠呼吸暂停严重程度:一项双盲、安慰剂对照、随机交叉试验。睡眠,2023 年;19(1):85-96。