医学
安慰剂
耐受性
曲唑酮
多导睡眠图
麻醉
阿托莫西汀
不利影响
内科学
呼吸暂停
注意缺陷多动障碍
哌醋甲酯
替代医学
抗抑郁药
病理
海马体
精神科
作者
Atqiya Aishah,Molly Kim,L. Gell,Daniel Vena,Ali Azarbarzin,Huy Pho,Daniel Norman,Joseph Ojile,Neda Esmaeili,Luigi Taranto‐Montemurro,Andrew Wellman,Scott A. Sands,Ludovico Messineo
出处
期刊:Thorax
[BMJ]
日期:2025-05-13
卷期号:80 (9): 641-649
被引量:1
标识
DOI:10.1136/thorax-2024-222513
摘要
Introduction Combination of the noradrenergic atomoxetine with either the antimuscarinic aroxybutynin or trazodone has been shown to improve obstructive sleep apnoea (OSA) severity. However, atomoxetine may contribute to apnoea-cycling and reduced drug tolerability due to wake-promoting, especially in a subgroup (poor cytochrome 2D6 metabolisers leading to higher blood concentration of medication). We investigated the effect of a potentially more manageable noradrenergic, viloxazine, with and without trazodone, on OSA severity. Methods In this double-blind, placebo-controlled, cross-over study, 24 patients with OSA (18–75 years) were analysed and randomised to 500 mg viloxazine, 500/75 mg viloxazine-trazodone (vilo-trazo) or placebo; taken before bed for 2 weeks with 1-week washout between treatments. In-laboratory polysomnography was performed at the end of each cross-over period. Mixed-model analyses compared the effect of vilo-trazo versus placebo on AHI 4 (apnoea-hypopnoea index with 4% desaturations; primary outcome) and hypoxic burden (secondary outcome). Additional outcomes examined the effects of vilo-trazo versus viloxazine on total sleep time (TST) and wake-after-sleep-onset (WASO). Safety endpoints (patient-reported outcomes, heart rate and adverse events) were also assessed. Results Vilo-trazo reduced AHI 4 (mean difference (95% CI): 10.5 (6.6, 13.6) events/hour, p<0.001) and hypoxic burden (16.7 (9.6, 21.8) %min/hr, p<0.001) versus placebo. Compared with viloxazine, TST tended to be longer on vilo-trazo (22.3 (−1.4, 46.0) min, p<0.065), while WASO was unchanged. TST and WASO remained significantly reduced on vilo-trazo versus placebo. Both interventions worsened patient-reported outcomes, although to a lesser extent on vilo-trazo, and increased heart rate versus placebo. Commonly reported adverse events were insomnia, constipation, headache and xerostomia. Conclusions Viloxazine-trazodone reduced OSA severity. Potential deleterious effects of viloxazine on sleep quality appeared partly attenuated by trazodone. Trial registration number NCT05793684 .
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