Angerbauer Raphael, Stefani Ambra, Zitser Jennifer, Ibrahim Abubaker, Anselmi Victoria, Süzgün Merve Aktan, Egger Kristin, Brandauer Elisabeth, Högl Birgit, Cesari Matteo
Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Sleep Center and Movement Disorders Unit, Neurology Department, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
J Sleep Res. 2025 Jun;34(3):e14351. doi: 10.1111/jsr.14351. Epub 2024 Sep 25.
Previous studies indicated that patients with isolated rapid eye movement (REM) sleep behaviour disorder (iRBD) exhibit alterations in spectral electroencephalographic (EEG), spindle, and slow-wave features. As it is currently unknown how these EEG features evolve over time, this study aimed to evaluate their temporal progression in patients with iRBD in comparison to controls. We included 23 patients with iRBD and 23 controls. Two polysomnographies (baseline and follow-up) were recorded with a mean (standard deviation) interval of 4.0 (2.5) years and were automatically analysed for sleep stages, spectral bandpower, spindles, and slow waves. We used linear models to evaluate differences at each time point, and linear mixed-effects models to analyse differences in temporal progression between the groups. At baseline, patients with iRBD presented EEG slowing both in REM (expressed as significantly reduced α-bandpower and increased δ-bandpower in frontal channels) and in non-REM (NREM) sleep (significantly increased slow-to-fast ratio in central channels). These differences vanished at follow-up. In both REM and NREM sleep, γ-bandpower was increased at follow-up in patients with iRBD, resulting in significantly different temporal progression between groups (in occipital channels during REM sleep and frontal channels during NREM sleep). Relative power of sleep spindles was significantly higher at baseline in patients with iRBD in frontal channels, but we observed a significant reduction over time in central channels. Finally, slow waves were significantly shorter in patients with iRBD at both time-points. Our results underscore the need of considering longitudinal data when analysing sleep EEG features in patients with iRBD. The observed temporal changes as markers of progression of neurodegeneration require further investigations.
先前的研究表明,患有孤立性快速眼动(REM)睡眠行为障碍(iRBD)的患者在频谱脑电图(EEG)、纺锤波和慢波特征方面存在改变。由于目前尚不清楚这些EEG特征如何随时间演变,本研究旨在评估iRBD患者与对照组相比这些特征的时间进展情况。我们纳入了23例iRBD患者和23例对照。记录了两次多导睡眠图(基线和随访),平均(标准差)间隔为4.0(2.5)年,并自动分析睡眠阶段、频谱带功率、纺锤波和慢波。我们使用线性模型评估每个时间点的差异,并使用线性混合效应模型分析两组之间时间进展的差异。在基线时,iRBD患者在REM睡眠(表现为额叶通道α带功率显著降低和δ带功率增加)和非REM(NREM)睡眠(中央通道慢-快比值显著增加)中均出现EEG减慢。这些差异在随访时消失。在REM和NREM睡眠中,iRBD患者在随访时γ带功率均增加,导致两组之间时间进展存在显著差异(REM睡眠期间枕叶通道和NREM睡眠期间额叶通道)。iRBD患者额叶通道睡眠纺锤波的相对功率在基线时显著更高,但我们观察到随着时间推移中央通道显著降低。最后,iRBD患者在两个时间点的慢波均显著更短。我们的结果强调在分析iRBD患者的睡眠EEG特征时需要考虑纵向数据。观察到的作为神经退行性变进展标志物的时间变化需要进一步研究。