Innsbruck Medical University, Department of Neurology, Innsbruck, Austria.
J Clin Sleep Med. 2013 Aug 15;9(8):805-12. doi: 10.5664/jcsm.2926.
Narcolepsy is reported to affect 26-56/100,000 in the general population. We aimed to describe clinical and polysomnographic features of a large narcolepsy cohort in order to comprehensively characterize the narcoleptic spectrum.
We performed a chart- and polysomnographybased review of all narcolepsy patients of the Innsbruck narcolepsy cohort.
A total of 100 consecutive narcolepsy patients (87 with cataplexy [NC], 13 without cataplexy [N]) were included in the analysis. All subjects had either excessive daytime sleepiness or cataplexy as their initial presenting clinical feature. Age at symptom onset was 20 (6-69) years. Diagnostic delay was 6.5 (0-39) years. The complete narcolepsy tetrad was present in 36/100 patients; 28/100 patients had three cardinal symptoms; 29/100 had two; and 7/100 had only excessive daytime sleepiness. Severity varied broadly with respect to excessive daytime sleepiness (median Epworth Sleepiness Scale score: 18, range 10-24), cataplexy (8-point Likert scale: median 4.5, range 1-8), hypnagogic hallucinations (median 4.5, range 1-7), and sleep paralysis (median 3, range 1-7). Sleep comorbidity was highly prevalent and ranged from sleeprelated movement disorders (n = 55/100), parasomnias (n = 34/100), and sleeprelated breathing disorders (n = 24/100), to insomnia (n = 28/100). REM sleep without atonia or a periodic limb movement in sleep index > 5/h were present in most patients (90/100 and 75/100). A high percentage of narcoleptic patients in the present study had high frequency leg movements (35%) and excessive fragmentary myoclonus (22%). Of the narcolepsy patients with clinical features of REM sleep behavior disorder (RBD), 76.5% had EMG evidence for RBD on the multiple sleep latency test (MSLT), based on a standard cutoff of a minimum of 18% of 3-sec miniepochs.
This study is one of the largest monocentric polysomnographic studies to date of patients with narcolepsy and confirms the frequent comorbidity of narcolepsy with many other sleep disorders. Our study is the first to evaluate the percentage of patients with high frequency leg movements and excessive fragmentary myoclonus in narcolepsy and is the first to demonstrate EMG evidence of RBD in the MSLT. These findings add to the growing body of literature suggesting that motor instability is a key feature of narcolepsy.
据报道,嗜睡症在普通人群中的发病率为 26-56/10 万。我们旨在描述一大群嗜睡症患者的临床和多导睡眠图特征,以便全面描述嗜睡症谱。
我们对因斯布鲁克嗜睡症队列中的所有嗜睡症患者进行了图表和多导睡眠图检查。
共纳入 100 例连续的嗜睡症患者(87 例伴猝倒[NC],13 例无猝倒[N])进行分析。所有患者均以日间过度嗜睡或猝倒为首发临床表现。症状发作年龄为 20(6-69)岁。诊断延迟 6.5(0-39)年。100 例患者中有 36 例存在完整的嗜睡四联症;28 例有三个主要症状;29 例有两个;7 例仅有日间过度嗜睡。日间过度嗜睡的严重程度差异较大(中位 Epworth 嗜睡量表评分:18,范围 10-24),猝倒(8 点 Likert 量表:中位 4.5,范围 1-8),催眠幻觉(中位 4.5,范围 1-7)和睡眠瘫痪(中位 3,范围 1-7)。睡眠共病非常普遍,包括睡眠相关运动障碍(n=55/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)、睡眠相关呼吸障碍(n=24/100)和失眠(n=28/100)。90/100 例和 75/100 例 REM 睡眠无动性或周期性肢体运动指数(PLMS)> 5/h 的患者比例较高。在本研究中,相当比例的嗜睡症患者存在高频腿部运动(35%)和过度片段性肌阵挛(22%)。在具有 REM 睡眠行为障碍(RBD)临床特征的嗜睡症患者中,76.5%的患者在多导睡眠图潜伏期试验(MSLT)上存在肌电图证据的 RBD,基于最小 3 秒微睡眠期的 18%的标准截断值。
本研究是迄今为止最大的单中心多导睡眠图研究之一,研究了嗜睡症患者的临床特征,证实了嗜睡症与许多其他睡眠障碍的常见共病。我们的研究首次评估了嗜睡症中高频腿部运动和过度片段性肌阵挛的患者比例,首次在 MSLT 中证明了 RBD 的肌电图证据。这些发现增加了越来越多的文献,表明运动不稳定是嗜睡症的一个关键特征。