Department of Neuroscience, Mayo Clinic, Jacksonville, Florida 32224, USA.
Mov Disord. 2012 Jan;27(1):72-8. doi: 10.1002/mds.24003. Epub 2011 Oct 28.
The purpose of this study was to determine whether dementia with Lewy bodies with and without probable rapid eye movement sleep behavior disorder differ clinically or pathologically. Patients with dementia with Lewy bodies (DLB) with probable rapid eye movement sleep behavior sleep disorder (n = 71) were compared with those without it (n = 19) on demographics, clinical variables (core features of dementia with Lewy bodies, dementia duration, rate of cognitive/motor changes), and pathologic indices (Lewy body distribution, neuritic plaque score, Braak neurofibrillary tangle stage). Individuals with probable rapid eye movement sleep behavior disorder were predominantly male (82% vs 47%) and had a shorter duration of dementia (mean, 8 vs 10 years), earlier onset of parkinsonism (mean, 2 vs 5 years), and earlier onset of visual hallucinations (mean, 3 vs 6 years). These patients also had a lower Braak neurofibrillary tangle stage (stage IV vs stage VI) and lower neuritic plaque scores (18% vs 85% frequency), but no difference in Lewy body distribution. When probable rapid eye movement sleep behavior disorder developed early (at or before dementia onset), the onset of parkinsonism and hallucinations was earlier and Braak neurofibrillary tangle stage was lower compared with those who developed the sleep disorder after dementia onset. Women with autopsy-confirmed DLB without a history of dream enactment behavior during sleep had a later onset of hallucinations and parkinsonism and a higher Braak NFT stage. Probable rapid eye movement sleep behavior disorder is associated with distinct clinical and pathologic characteristics of dementia with Lewy bodies.
这项研究的目的是确定路易体痴呆伴或不伴可能的快速眼动睡眠行为障碍在临床和病理上是否存在差异。将路易体痴呆伴可能的快速眼动睡眠行为障碍患者(n=71)与不伴该病的患者(n=19)进行比较,比较内容包括人口统计学资料、临床变量(路易体痴呆的核心特征、痴呆持续时间、认知/运动变化率)和病理指标(路易体分布、神经原纤维缠结Braak 分期、神经纤维缠结神经丝缠结阶段)。可能的快速眼动睡眠行为障碍患者主要为男性(82%比 47%),痴呆持续时间较短(平均 8 年比 10 年),帕金森病起病较早(平均 2 年比 5 年),视幻觉起病较早(平均 3 年比 6 年)。这些患者的 Braak 神经丝缠结分期较低(IV 期比 VI 期),神经原纤维缠结斑块评分较低(18%比 85%的频率),但路易体分布无差异。当快速眼动睡眠行为障碍可能在早期(在痴呆发病之前或同时)发生时,帕金森病和幻觉的起病更早,Braak 神经丝缠结分期更低,而在痴呆发病后发生该睡眠障碍的患者则相反。在尸检确诊的无睡眠中梦动行为史的路易体痴呆女性中,幻觉和帕金森病的起病较晚,Braak 神经丝缠结分级较高。可能的快速眼动睡眠行为障碍与路易体痴呆的独特临床和病理特征有关。