Department of Neurology, McGill University, Montreal General Hospital, Montreal, Canada.
Neurology. 2010 Jan 19;74(3):239-44. doi: 10.1212/WNL.0b013e3181ca0166.
Over 50% of persons with idiopathic REM sleep behavior disorder (RBD) will develop Parkinson disease (PD) or dementia. At present, there is no way to predict who will develop disease. Since polysomnography is performed in all patients with idiopathic RBD at diagnosis, there is an opportunity to analyze if baseline sleep variables predict eventual neurodegenerative disease.
In a longitudinally studied cohort of patients with idiopathic RBD, we identified those who had developed neurodegenerative disease. These patients were matched by age, sex, and follow-up duration to patients with RBD who remained disease-free and to controls. Polysomnographic variables at baseline (i.e., before development of neurodegenerative disease) were compared between groups.
Twenty-six patients who developed neurodegenerative disease were included (PD 12, multiple system atrophy 1, dementia 13). The interval between polysomnogram and disease onset was 6.7 years, mean age was 69.5, and 81% were male. There were no differences between groups in sleep latency, sleep time, % stages 2-4, % REM sleep, or sleep efficiency. However, patients with idiopathic RBD who developed neurodegenerative disease had increased tonic chin EMG activity during REM sleep at baseline compared to those who remained disease-free (62.7 +/- 6.0% vs 41.0 +/- 6.0%, p = 0.020). This effect was seen only in patients who developed PD (72.9 +/- 6.0% vs 41.0 +/- 6.0%, p = 0.002), and not in those who developed dementia (54.3 +/- 10.3, p = 0.28). There was no difference in phasic submental REM EMG activity between groups.
In patients with REM sleep behavior disorder initially free of neurodegenerative disease, the severity of REM atonia loss on baseline polysomnogram predicts the development of Parkinson disease.
超过 50%的特发性 REM 睡眠行为障碍(RBD)患者会发展为帕金森病(PD)或痴呆。目前,尚无方法预测谁会患上疾病。由于所有特发性 RBD 患者在诊断时都进行了多导睡眠图检查,因此有机会分析基线睡眠变量是否可以预测最终的神经退行性疾病。
在一项对特发性 RBD 患者进行的纵向研究队列中,我们确定了那些已经患上神经退行性疾病的患者。这些患者按年龄、性别和随访时间与无疾病的 RBD 患者和对照组患者相匹配。比较了各组患者在基线时(即在发生神经退行性疾病之前)的多导睡眠图变量。
共纳入了 26 名患有神经退行性疾病的患者(PD12 例,多系统萎缩 1 例,痴呆 13 例)。多导睡眠图与疾病发作之间的间隔为 6.7 年,平均年龄为 69.5 岁,81%为男性。睡眠潜伏期、睡眠时间、2-4 期睡眠百分比、REM 睡眠时间和睡眠效率在各组之间无差异。然而,与无疾病的患者相比,患有特发性 RBD 并发展为神经退行性疾病的患者在 REM 睡眠期间的颏肌紧张性肌电活动增加(62.7 +/- 6.0%对 41.0 +/- 6.0%,p = 0.020)。这种效应仅见于发展为 PD 的患者(72.9 +/- 6.0%对 41.0 +/- 6.0%,p = 0.002),而发展为痴呆的患者则无差异(54.3 +/- 10.3,p = 0.28)。各组间颏下 REM 肌电活动的相位差异无统计学意义。
在最初无神经退行性疾病的 REM 睡眠行为障碍患者中,基线多导睡眠图上 REM 弛缓丧失的严重程度预测了帕金森病的发展。