孤立的快速眼动睡眠行为障碍与24小时休息活动测量的改变有关

Joseph R. Winer, Renske Lok, Adrian Ekelmans, Flavia Bueno, Kathleen L. Poston, Jamie M. Zeitzer, Emmanuel H. During
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摘要

孤立性快速眼动睡眠行为障碍(iRBD)是指快速眼动睡眠过程中运动抑制的丧失,是路易体病的前驱症状,超过80%的iRBD患者会发展为帕金森病或路易体痴呆。休息-活动模式的破坏是帕金森病的一个已建立的预测因子,但在iRBD患者中尚未得到很好的表征。在这里,我们验证了基于加速度计的24小时活动测量的假设,即相对于匹配的健康对照,iRBD患者的碎片性和可变性更大。材料与方法38例iRBD患者使用Axivity腕带加速度计监测24小时活动(平均±SD) 24.6±8.8天。选择年龄、性别和体重指数匹配的健康老年人(N = 119)作为对照。处理原始加速度计数据,计算24小时活动的非参数和余弦测量。功能主成分分析(fPCA)用于检测24小时活动模式的差异。结果与匹配的对照组相比,iRBD患者在最活跃的10小时内,其余弦振幅、中观和活动显著降低,反映了整体活动水平较低和活动中断。他们在夜间的活动也明显增加(L5)。FPCA表明,白天活动减少和夜间活动增加可以解释iRBD中观察到的总体差异。结论休息-活动节律的多个指标支持iRBD中24小时活动测量改变的假设。这种功能障碍可能反映了睡眠-觉醒调节回路的退化,这是iRBD的一种症状,表明路易体病的早期阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated REM sleep behavior disorder is associated with altered 24-h rest-activity measures
Introduction Isolated REM sleep behavior disorder (iRBD), the loss of motor inhibition during REM sleep, is a symptom of prodromal Lewy body disease, with over 80% of iRBD patients progressing to Parkinson's disease or dementia with Lewy bodies. Disruption of rest-activity patterns, an established predictor of Parkinson's disease, has not been well characterized in patients with iRBD. Here, we tested the hypothesis that accelerometer-based measures of 24-h activity would indicate greater fragmentation and variability in patients with iRBD relative to matched healthy controls. Materials and methods Patients with iRBD ( N = 38) had 24-h activity monitored for (mean ± SD) 24.6 ± 8.8 days using an Axivity wrist-worn accelerometer. Age, sex, and body mass index matched healthy older adults ( N = 119) were selected as controls. Raw accelerometer data were processed and nonparametric and cosinor measures of 24-h activity were calculated. Functional principal component analyses (fPCA) were applied to detect differences in 24-h activity patterns. Results Compared to matched controls, individuals with iRBD had significantly lower cosine amplitude, mesor, and activity during their most active 10 hours, reflecting overall lower levels of activity and disrupted activity. They also had significantly increased movement during the night (L5). FPCA indicated that decreased daytime and increased nighttime activity may explain overall differences observed in iRBD. Conclusion Multiple metrics of rest-activity rhythms support the hypothesis that 24-h activity measures are altered in iRBD. This dysfunction may reflect degeneration of sleep-wake regulating circuits, representing a symptom of iRBD and indicating the early stages of Lewy body disease.
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