Arnulf I, Konofal E, Merino-Andreu M, Houeto J L, Mesnage V, Welter M L, Lacomblez L, Golmard J L, Derenne J P, Agid Y
Fédération des Pathologies du Sommeil, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.
Neurology. 2002 Apr 9;58(7):1019-24. doi: 10.1212/wnl.58.7.1019.
To investigate the potential causes of excessive daytime sleepiness in patients with PD-poor sleep quality, abnormal sleep-wakefulness control, and treatment with dopaminergic agents.
The authors performed night-time polysomnography and daytime multiple sleep latency tests in 54 consecutive levodopa-treated patients with PD referred for sleepiness, 27 of whom were also receiving dopaminergic agonists.
Sleep latency was 6.3 +/- 0.6 minutes (normal >8 minutes), and the Epworth Sleepiness score was 14.3 +/- 4.1 (normal <10). A narcolepsy-like phenotype (> or = 2 sleep-onset REM periods) was found in 39% of the patients, who were sleepier (4.6 +/- 0.9 minutes) than the other 61% of patients (7.4 +/- 0.7 minutes). Periodic leg movement syndromes were rare (15%, range 16 to 43/h), but obstructive sleep apnea-hypopnea syndromes were frequent (20% of patients had an apnea-hypopnea index >15/h; range 15.1 to 50.0). Severity of sleepiness was weakly correlated with Epworth Sleepiness score (r = -0.34) and daily dose of levodopa (r = 0.30) but not with dopamine-agonist treatment, age, disease duration, parkinsonian motor disability, total sleep time, periodic leg movement, apnea-hypopnea, or arousal indices.
In patients with PD preselected for sleepiness, severity of sleepiness was not dependent on nocturnal sleep abnormalities, motor and cognitive impairment, or antiparkinsonian treatment. The results suggest that sleepiness-sudden onset of sleep-does not result from pharmacotherapy but is related to the pathology of PD.
探讨帕金森病(PD)患者日间过度嗜睡的潜在原因——睡眠质量差、睡眠-觉醒控制异常以及多巴胺能药物治疗。
作者对54例因嗜睡前来就诊且连续接受左旋多巴治疗的PD患者进行了夜间多导睡眠图和日间多次睡眠潜伏期测试,其中27例患者还接受了多巴胺能激动剂治疗。
睡眠潜伏期为6.3±0.6分钟(正常>8分钟),爱泼沃斯嗜睡量表(Epworth Sleepiness)评分为14.3±4.1(正常<10)。39%的患者出现发作性睡病样表型(≥2个睡眠起始快速眼动期),这些患者比其他61%的患者更嗜睡(4.6±0.9分钟 vs 7.4±0.7分钟)。周期性肢体运动综合征少见(15%,范围为16至43次/小时),但阻塞性睡眠呼吸暂停低通气综合征常见(20%的患者呼吸暂停低通气指数>15次/小时;范围为15.1至50.0)。嗜睡严重程度与爱泼沃斯嗜睡量表评分(r = -0.34)和左旋多巴日剂量(r = 0.30)弱相关,但与多巴胺能激动剂治疗、年龄、病程、帕金森病运动功能障碍、总睡眠时间、周期性肢体运动、呼吸暂停低通气或觉醒指数无关。
在因嗜睡而入选的PD患者中,嗜睡严重程度不依赖于夜间睡眠异常、运动和认知障碍或抗帕金森病治疗。结果表明,嗜睡——突然入睡——并非由药物治疗引起,而是与PD的病理改变有关。