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与绝经后综合征及激素替代疗法相关的失眠:关于患者与对照者基线差异的睡眠实验室研究,以及关于新型雌激素 - 孕激素组合(Climodien,Lafamme)与单独使用雌激素效果对比的双盲、安慰剂对照研究。

Insomnia related to postmenopausal syndrome and hormone replacement therapy: sleep laboratory studies on baseline differences between patients and controls and double-blind, placebo-controlled investigations on the effects of a novel estrogen-progestogen combination (Climodien, Lafamme) versus estrogen alone.

作者信息

Saletu-Zyhlarz Gerda, Anderer Peter, Gruber Georg, Mandl Magdalena, Gruber Doris, Metka Markus, Huber Johannes, Oettel Michael, Gräser Thomas, Abu-Bakr Manal Hassan, Grätzhofer Elisabeth, Saletu Bernd

机构信息

Department of Psychiatry, University of Vienna, Vienna, Austria.

出版信息

J Sleep Res. 2003 Sep;12(3):239-54. doi: 10.1046/j.1365-2869.2003.00356.x.

Abstract

Differences in sleep and awakening quality between 51 insomniac postmenopausal syndrome patients and normal controls were evaluated. In a subsequent double-blind, placebo-controlled, comparative, randomized, three-arm trial (Climodien 2/3 = estradiol valerate 2 mg + the progestogen dienogest 3 mg = regimen A, estradiol valerate 2 mg = regimen EV, and placebo = regimen P), the effects of 2 months of hormone replacement therapy were investigated, followed by a 2-month open-label phase in which all patients received Climodien 2/2 (EV 2 mg + dienogest 2 mg = regimen A*). Polysomnography at baseline demonstrated significantly deteriorated sleep initiation and maintenance, increased S1 and decreased S2 in patients. Subjective sleep and awakening quality, well-being, morning drive, wakefulness, memory and reaction time performance were deteriorated too. Treatment with both regimen A and regimen EV induced a moderate, although nonsignificant, improvement in the primary efficacy variable wakefulness during the total sleep period compared with baseline, while under placebo no changes occurred. Secondary efficacy variables concerning sleep initiation and maintenance, and sleep architecture showed similar findings. The apnea and apnea-hypopnea indices improved significantly under regimen A, compared with both baseline and placebo. Subjective sleep and awakening quality improved significantly after regimen A and EV compared with baseline, with the drug-induced changes being superior to those induced by placebo. In the open-label phase, subjective sleep quality improved further, significantly in the former regimen A group. Awakening quality, somatic complaints and morning thymopsyche did not yield any significant findings. Concerning morning noopsychic performance, memory improved significantly after regimen A compared with baseline, fine motor activity after regimen EV. Reaction time performance increased with all three compounds. In conclusion, Climodien significantly improved subjective sleep quality, the apnea and apnea-hypopnea indices of insomniac postmenopausal syndrome patients, while it only marginally improved variables concerning objective sleep and awakening quality.

摘要

评估了51例失眠绝经后综合征患者与正常对照者在睡眠和觉醒质量上的差异。在随后的一项双盲、安慰剂对照、比较性、随机、三臂试验(克龄蒙2/3 = 戊酸雌二醇2 mg + 孕激素地诺孕素3 mg = 方案A,戊酸雌二醇2 mg = 戊酸雌二醇方案,安慰剂 = 方案P)中,研究了2个月激素替代疗法的效果,随后是为期2个月的开放标签阶段,在此阶段所有患者均接受克龄蒙2/2(戊酸雌二醇2 mg + 地诺孕素2 mg = 方案A*)。基线时的多导睡眠图显示患者的睡眠起始和维持显著恶化,S1增加而S2减少。主观睡眠和觉醒质量、幸福感、晨醒驱动力、清醒度、记忆力和反应时间表现也都恶化。与基线相比,方案A和戊酸雌二醇方案治疗均使主要疗效变量总睡眠时间内的清醒度有中度改善,虽不显著,而安慰剂组无变化。关于睡眠起始和维持以及睡眠结构的次要疗效变量显示出类似结果。与基线和安慰剂相比,方案A治疗下呼吸暂停和呼吸暂停低通气指数显著改善。与基线相比,方案A和戊酸雌二醇方案治疗后主观睡眠和觉醒质量显著改善,药物引起的变化优于安慰剂引起的变化。在开放标签阶段,主观睡眠质量进一步改善,在前方案A组中显著改善。觉醒质量、躯体不适和晨醒心理状态未得出任何显著结果。关于晨醒精神运动表现,与基线相比,方案A治疗后记忆力显著改善,戊酸雌二醇方案治疗后精细运动活动改善。三种化合物治疗后反应时间表现均增加。总之,克龄蒙显著改善了失眠绝经后综合征患者的主观睡眠质量、呼吸暂停和呼吸暂停低通气指数,而仅略微改善了与客观睡眠和觉醒质量相关的变量。

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