Department of Neurology, McGill University, Montreal General Hospital, Montreal, Quebec, Canada.
Parkinsonism Relat Disord. 2013 Jul;19(7):670-5. doi: 10.1016/j.parkreldis.2013.03.003. Epub 2013 Apr 2.
Although a variety of pharmacologic and non-pharmacologic treatments are effective for insomnia in the general population, insomnia in Parkinson's disease differs in important ways and may need different treatments. No studies have conclusively demonstrated effective insomnia treatments in Parkinson's disease.
We conducted a three-arm six-week randomized pilot study assessing non-pharmacologic treatment (cognitive behavioural therapy with bright light therapy) or doxepin (10 mg daily), compared to an inactive placebo in Parkinson's patients with insomnia. Sleep outcomes included insomnia scales, clinical global impression, sleep diaries and actigraphy. Secondary outcomes included motor severity, fatigue, depression and quality of life.
18 patients were randomized, 6 to each group. Compared to placebo, doxepin improved the Insomnia Severity Index (-9 ± 5.4 vs. -2 ± 3.9, p = 0.03), the SCOPA-night score (-5.2 ± 1.5 vs. -2.3 ± 2.8, p = 0.049), the Pittsburgh Sleep Quality Index-sleep disturbances subscale (-0.5 ± 0.5 vs 0.2 ± 0.4, p = 0.02), and both patient and examiner-rated clinical global impression of change (1.7 ± 0.8 vs. 0.5 ± 0.8, p = 0.03 and 1.4 ± 0.5 vs. 0.3 ± 0.5, p = 0.003). On secondary outcomes doxepin reduced the fatigue severity scale (p = 0.02) and improved scores on the Montreal Cognitive Assessment (p = 0.007). Non-pharmacological treatment reduced the Insomnia Severity Index (-7.8 ± 3.8 vs. -2.0 ± 3.9, p = 0.03), and the examiner-reported clinical global impression of change (p = 0.006), but was associated with decline in Parkinson Disease Questionnaire-39. There were no changes in other primary and secondary outcomes, including actigraphy outcomes. Adverse events were comparable in all groups.
Doxepin and non-pharmacologic treatment substantially improved insomnia in Parkinson's disease. These potential benefits must be replicated in a full confirmatory randomized controlled trial.
尽管各种药物和非药物治疗方法对普通人群的失眠症都有效,但帕金森病患者的失眠症在重要方面存在差异,可能需要不同的治疗方法。目前还没有研究明确证明对帕金森病失眠症有效的治疗方法。
我们进行了一项三臂六周随机试点研究,评估非药物治疗(认知行为疗法联合亮光疗法)或多塞平(每日 10 毫克)与帕金森病伴失眠症患者的安慰剂相比的疗效。睡眠结果包括失眠量表、临床总体印象、睡眠日记和活动记录仪。次要结果包括运动严重程度、疲劳、抑郁和生活质量。
18 名患者被随机分为 3 组,每组 6 名。与安慰剂相比,多塞平改善了失眠严重程度指数(-9 ± 5.4 与-2 ± 3.9,p = 0.03)、SCOPA-night 评分(-5.2 ± 1.5 与-2.3 ± 2.8,p = 0.049)、匹兹堡睡眠质量指数睡眠障碍子量表(-0.5 ± 0.5 与 0.2 ± 0.4,p = 0.02),以及患者和检查者评估的临床总体印象变化(1.7 ± 0.8 与 0.5 ± 0.8,p = 0.03 和 1.4 ± 0.5 与 0.3 ± 0.5,p = 0.003)。在次要结果中,多塞平降低了疲劳严重程度量表(p = 0.02)和蒙特利尔认知评估量表的评分(p = 0.007)。非药物治疗降低了失眠严重程度指数(-7.8 ± 3.8 与-2.0 ± 3.9,p = 0.03)和检查者报告的临床总体印象变化(p = 0.006),但与帕金森病问卷-39 评分下降有关。其他主要和次要结局,包括活动记录仪结果,均无变化。所有组的不良事件相似。
多塞平和非药物治疗显著改善了帕金森病患者的失眠症。这些潜在的益处必须在一项充分的确认性随机对照试验中得到复制。