Boeve B F, Silber M H, Ferman T J, Kokmen E, Smith G E, Ivnik R J, Parisi J E, Olson E J, Petersen R C
Sleep Disorders Center, Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Neurology. 1998 Aug;51(2):363-70. doi: 10.1212/wnl.51.2.363.
REM sleep behavior disorder (RBD) has been reported with various neurodegenerative disorders, most frequently in disorders with Lewy body pathology. RBD often precedes the onset of PD, and a recent prospective study showed that 38% of patients with RBD eventually developed PD.
We identified 37 patients with degenerative dementia and a history of bursts of vigorous movement of the arms and legs with vocalization during sleep and associated with dream recall. Patients with and without two or more signs of parkinsonism were compared. Clinical, laboratory, and neuropsychometric features were analyzed, and criteria for the clinical diagnosis of dementia with Lewy bodies (DLB) were applied to all patients.
Thirty-four of the 37 patients were male with mean age at onset of 61.5 years for RBD and 68.1 years for cognitive decline. RBD commenced before or concurrently with dementia in all patients but two. Parkinsonism (two or more signs) occurred in 54% of the sample (20/37), with a mean age at onset of 69.1 years. Polysomnography (PSG) confirmed RBD in all patients studied. Neuropsychological testing demonstrated impaired perceptual-organizational skills, verbal fluency, and marked constructional dyspraxia in more than one-half the patients. There were no statistically significant differences in the frequency of clinical features or in neuropsychological performance between patients with and without parkinsonism. Thirty-four patients (92%) met criteria for clinically possible or probable DLB. Three patients were autopsied; all had limbic with or without neocortical Lewy bodies.
We report a group of predominantly male patients with a characteristic association of RBD and degenerative dementia. The clinical and neuropsychometric features of the groups of patients with and without parkinsonism are similar. We hypothesize that the underlying pathology in these patients is DLB.
快速眼动睡眠行为障碍(RBD)已在多种神经退行性疾病中被报道,最常见于伴有路易小体病理改变的疾病。RBD常先于帕金森病(PD)发病,最近一项前瞻性研究表明,38%的RBD患者最终发展为PD。
我们确定了37例患有退行性痴呆且有睡眠期间手臂和腿部剧烈运动伴发声并与梦境回忆相关病史的患者。比较有和没有两种或更多帕金森病体征的患者。分析临床、实验室和神经心理测量特征,并将路易体痴呆(DLB)的临床诊断标准应用于所有患者。
37例患者中有34例为男性,RBD发病的平均年龄为61.5岁,认知功能下降发病的平均年龄为68.1岁。除2例患者外,所有患者的RBD均在痴呆之前或同时开始。54%的样本(20/37)出现帕金森病体征(两种或更多体征),发病的平均年龄为69.1岁。多导睡眠图(PSG)证实所有研究患者均有RBD。神经心理学测试显示,超过一半的患者存在感知组织技能受损、语言流畅性受损和明显的结构性失用症。有和没有帕金森病体征的患者在临床特征频率或神经心理表现方面没有统计学上的显著差异。34例患者(92%)符合临床可能或很可能的DLB标准。3例患者接受了尸检;所有患者均有边缘系统路易小体,部分伴有或不伴有新皮质路易小体。
我们报告了一组以男性为主的患者,其具有RBD与退行性痴呆的特征性关联。有和没有帕金森病体征的患者组的临床和神经心理测量特征相似。我们推测这些患者的潜在病理是DLB。