Sasai Taeko, Matsuura Masato, Inoue Yuichi
Japan Somnology Center, Neuropsychiatric Research Institute, Tokyo, Japan ; Yoyogi Sleep Disorder Clinic, Tokyo, Japan ; Department of Somnology, Tokyo Medical University, Tokyo, Japan ; Department of Life Sciences and Bioinformatics, Division of Biomedical Laboratory Sciences, Graduate School of Health Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Sleep. 2013 Dec 1;36(12):1893-9. doi: 10.5665/sleep.3224.
Mild cognitive impairment (MCI) and electroencephalographic (EEG) slowing have been reported as common findings of idiopathic rapid eye movement (REM) sleep behavior disorder (iRBD) and α-synucleinopathies. The objective of this study is to clarify the relation between MCI and physiological markers in iRBD.
Cross-sectional study.
Yoyogi Sleep Disorder Center.
Thirty-one patients with iRBD including 17 younger patients with iRBD (younger than 70 y) and 17 control patients for the younger patients with iRBD.
N/A.
Montreal Cognitive Assessment (MoCA) and n-polysomnogram (PSG) were conducted of all participants. In patients with iRBD, the factors associated with MCI were explored among parameters of REM sleep without atonia (RWA), score of Sniffin' Sticks Test (threshold-discrimination-identification [TDI] score), RBD morbidity, and RBD severity evaluated with the Japanese version of the RBD questionnaire (RBDQ-JP). The younger iRBD group showed significantly lower alpha power during wake and lower MoCA score than the age-matched control group. MCI was detected in 13 of 17 patients (76.5%) on MoCA in this group. Among patients wtih iRBD, the MoCA score negatively correlated with age, proportion of slow wave sleep, TDI score, and EEG spectral power. Multiple regression analysis provided the following equation: MoCA score = 50.871-0.116age -5.307log (δ power during REM sleep) + 0.086*TDI score (R² = 0.598, P < 0.01). The standardized partial regression coefficients were -0.558 for age, -0.491 for log (δ power during REM sleep), and 0.357 for TDI score (F = 9.900, P < 0.001).
Electroencephalographic slowing, especially during rapid eye movement sleep and olfactory dysfunction, was revealed to be associated with cognitive decline in idiopathic rapid eye movement sleep behavior disorder.
轻度认知障碍(MCI)和脑电图(EEG)减慢已被报道为特发性快速眼动(REM)睡眠行为障碍(iRBD)和α-突触核蛋白病的常见表现。本研究的目的是阐明iRBD中MCI与生理标志物之间的关系。
横断面研究。
代代木睡眠障碍中心。
31例iRBD患者,包括17例年龄较轻的iRBD患者(年龄小于70岁)以及17例年龄较轻的iRBD患者的对照患者。
无。
对所有参与者进行蒙特利尔认知评估(MoCA)和整夜多导睡眠图(PSG)检查。在iRBD患者中,在无张力快速眼动睡眠(RWA)参数、嗅觉棒测试得分(阈值-辨别-识别[TDI]得分)、RBD发病率以及用日语版RBD问卷(RBDQ-JP)评估的RBD严重程度中探索与MCI相关的因素。年龄较轻的iRBD组在清醒时的α波功率显著低于年龄匹配的对照组,且MoCA得分更低。该组中17例患者中有13例(76.5%)通过MoCA检测出MCI。在iRBD患者中,MoCA得分与年龄、慢波睡眠比例、TDI得分和EEG频谱功率呈负相关。多元回归分析得出以下方程:MoCA得分 = 50.871 - 0.116×年龄 - 5.307×log(快速眼动睡眠期间的δ波功率) + 0.086×TDI得分(R² = 0.598,P < 0.01)。年龄的标准化偏回归系数为 -0.558,log(快速眼动睡眠期间的δ波功率)为 -0.491,TDI得分为0.357(F = 9.900,P < 0.001)。
脑电图减慢,尤其是在快速眼动睡眠期间以及嗅觉功能障碍,被发现与特发性快速眼动睡眠行为障碍中的认知衰退有关。