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Effects of tiagabine on slow wave sleep and arousal threshold in patients with obstructive sleep apnea

机译:钛滨对阻塞性睡眠呼吸暂停患者慢波睡眠与唤醒阈值的影响

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ABSTRACT: Introduction: Obstructive sleep apnea (OSA) severity is markedly reduced during slow-wave sleep (SWS) even in patients with a severe disease. The reason for this improvement is uncertain but likely relates to non-anatomical factors (i.e. reduced arousability, chemosensitivity, and increased dilator muscle activity). The anticonvulsant tiagabine produces a dose-dependent increase in SWS in subjects without OSA. This study aimed to test the hypothesis that tiagabine would reduce OSA severity by raising the overall arousal threshold during sleep. Aims and Methods: After a baseline physiology night to assess patients' OSA phenotypic traits, a placebo-controlled, double-blind, crossover trial of tiagabine 12 mg administered before sleep was performed in 14 OSA patients. Under each condition, we assessed the effects on sleep and OSA severity using standard clinical polysomnography. Results: Tiagabine increased slow-wave activity (SWA) of the electroencephalogram (1-4 Hz) compared to placebo (1.8 [0.4] vs. 2.0 [0.5] Log?V2, p = .04) but did not reduce OSA severity (apnea-hypopnea index [AHI] 41.5 [20.3] vs. 39.1 [16.5], p > .5). SWS duration (25 [20] vs. 26 [43] mins, p > .5) and arousal threshold (?26.5 [5.0] vs. ?27.6 [5.1] cmH2O, p = .26) were also unchanged between nights. Conclusions: Tiagabine modified sleep microstructure (increase in SWA) but did not change the duration of SWS, OSA severity, or arousal threshold in this group of OSA patients. Based on these findings, tiagabine should not be considered as a therapeutic option for OSA treatment.
机译:摘要:简介:在患有严重疾病的患者中,梗阻性睡眠呼吸暂停(OSA)严重程度显着降低了慢波睡眠(SWS)。这种改进的原因是不确定,但可能涉及非解剖因子(即减少棘突性,化学敏感度和扩张肌肉活性增加)。抗惊厥药钛合滨在没有OSA的受试者中产生的剂量依赖性增加。本研究旨在测试Tiagabine通过在睡眠期间提高整个唤醒阈值来减少OSA严重程度的假设。目的和方法:在基线生理学夜间评估患者的OSA表型特征,在14例患者中进行睡眠前施用的钛合滨12毫克的安慰剂控制,双盲,交叉试验。在每种情况下,我们使用标准临床多面程评估对睡眠和OSA严重程度的影响。结果:与安慰剂相比,噻吩并增加了脑电图(1-4Hz)的慢波活动(1-4 Hz)(1.8 [0.4],对数值,log?v2,p = .04),但没有减少OSA严重程度(呼吸暂停 - 缺氧指数[AHI] 41.5 [20.3]与39.1 [16.5],P> .5)。 SWS持续时间(25 [20]与26 [43] min,p> .5)和唤醒阈值(α26.5[5.0]与α27.6[5.1] CMH2O,P = .26)也不改变。结论:钛合滨改性睡眠微观结构(SWA增加)但没有改变这组OSA患者的SWS,OSA严重程度或唤醒阈值的持续时间。基于这些发现,噻嗪不应被视为OSA治疗的治疗选择。

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