维洛嗪和曲唑酮对阻塞性睡眠呼吸暂停的影响:一项随机、安慰剂对照、交叉研究。

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM
Thorax Pub Date : 2025-05-13 DOI:10.1136/thorax-2024-222513
Atqiya Aishah,Molly Kim,Laura Gell,Daniel Vena,Ali Azarbarzin,Huy Pho,Daniel Norman,Joseph Ojile,Neda Esmaeili,Luigi Taranto-Montemurro,Andrew Wellman,Scott Sands,Ludovico Messineo
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引用次数: 0

摘要

去甲肾上腺素能阿托西汀与抗uscarinic阿oxy布宁或曲唑酮联合使用已被证明可改善阻塞性睡眠呼吸暂停(OSA)的严重程度。然而,由于唤醒作用,托莫西汀可能导致呼吸暂停循环和药物耐受性降低,特别是在一个亚组中(细胞色素2D6代谢不良导致血药浓度升高)。我们研究了一种可能更易于管理的去肾上腺素能药物,维洛嗪,与曲唑酮和不含曲唑酮,对OSA严重程度的影响。方法在这项双盲、安慰剂对照、交叉研究中,对24例OSA患者(18-75岁)进行分析,并随机分配至500mg维洛嗪、500/ 75mg维洛嗪-曲唑酮(vilo-trazo)或安慰剂组;睡前服用2周,两次治疗之间间隔1周。在每个交叉期结束时进行实验室多导睡眠图检查。混合模型分析比较了vilo-trazo和安慰剂对AHI4(呼吸暂停-低通气指数)的影响,低通气指数为4%;主要结局)和缺氧负担(次要结局)。其他结果检验了vilo-trazo与viloxazine对总睡眠时间(TST)和睡眠后觉醒(WASO)的影响。安全性终点(患者报告的结局、心率和不良事件)也进行了评估。结果与安慰剂相比,vilo -trazo降低了AHI4(平均差异(95% CI): 10.5(6.6, 13.6)事件/小时,p<0.001)和缺氧负担(16.7 (9.6,21.8)%min/hr, p<0.001)。与viloxazine相比,vilo-trazo组的TST更长(22.3 (-1.4,46.0)min, p<0.065),而WASO不变。与安慰剂相比,vilo-trazo组的TST和WASO仍显著降低。两种干预措施都使患者报告的结果恶化,尽管vilo-trazo的程度较轻,并且与安慰剂相比心率增加。常见的不良反应是失眠、便秘、头痛和口干。结论斯维洛嗪-曲唑酮可降低OSA严重程度。维洛嗪对睡眠质量的潜在有害影响被曲唑酮部分减弱。试验注册号05793684。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of viloxazine and trazodone in obstructive sleep apnoea: a randomised, placebo-controlled, cross-over study.
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 AHI4 (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 AHI4 (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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来源期刊
Thorax
Thorax 医学-呼吸系统
CiteScore
16.10
自引率
2.00%
发文量
197
审稿时长
1 months
期刊介绍: Thorax stands as one of the premier respiratory medicine journals globally, featuring clinical and experimental research articles spanning respiratory medicine, pediatrics, immunology, pharmacology, pathology, and surgery. The journal's mission is to publish noteworthy advancements in scientific understanding that are poised to influence clinical practice significantly. This encompasses articles delving into basic and translational mechanisms applicable to clinical material, covering areas such as cell and molecular biology, genetics, epidemiology, and immunology.
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