Dong Menglong, Fan Mengmeng, Wang Yi, Lin Zhifeng, Zhao Xianchao, Chen Guoyan, Zhang Liping, Su Changjun, Cheng Jin-Xiang
Department of Neurology, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710038, China.
Sleep Breath. 2025 Aug 4;29(4):261. doi: 10.1007/s11325-025-03411-2.
The study investigated the differences in sleep electroencephalography characteristics between obstructive sleep apnea (OSA) patients with and without excessive daytime sleepiness (EDS), aiming to explore mechanisms underlying the development of EDS in OSA.
Sixty-one adult OSA patients were divided into OSA + EDS and OSA - EDS groups based on the Epworth Sleepiness Scale (ESS). Electroencephalography (EEG) data were analyzed for power spectral density (PSD) and functional connectivity using coherence and weighted phase lag index (wPLI).
Compared to the OSA - EDS group, the OSA + EDS group exhibited: (1) More severe nocturnal hypoxia during non-rapid eye movement (NREM) sleep; (2) Increased gamma band PSD during NREM stages 1-2; (3) Enhanced wPLI in the delta band during NREM stage 1 and wakefulness, correlated positively with the severity of OSA.
OSA patients with EDS show distinct neurophysiological patterns characterized by gamma hyperactivation during light sleep and compensatory delta-band synchronization during sleep-wake transition phase. Respiratory events may disrupt EEG dynamics in specific frequency bands, contributing to sleep instability and EDS. These findings highlight the importance of NREM sleep disruption and support tailored therapeutic interventions targeting cortical instability in OSA patients with persistent EDS.
本研究调查了伴有和不伴有日间过度嗜睡(EDS)的阻塞性睡眠呼吸暂停(OSA)患者睡眠脑电图特征的差异,旨在探索OSA患者发生EDS的潜在机制。
根据爱泼华嗜睡量表(ESS),将61例成年OSA患者分为OSA+EDS组和OSA-EDS组。使用相干性和加权相位滞后指数(wPLI)分析脑电图(EEG)数据的功率谱密度(PSD)和功能连接性。
与OSA-EDS组相比,OSA+EDS组表现出:(1)非快速眼动(NREM)睡眠期间夜间缺氧更严重;(2)NREM 1-2期γ波段PSD增加;(3)NREM 1期和清醒期间δ波段wPLI增强,与OSA严重程度呈正相关。
伴有EDS的OSA患者表现出独特的神经生理模式,其特征为浅睡眠期间γ波过度激活以及睡眠-觉醒转换期δ波段代偿性同步化。呼吸事件可能扰乱特定频段的脑电图动态,导致睡眠不稳定和EDS。这些发现凸显了NREM睡眠中断的重要性,并支持针对持续性EDS的OSA患者皮质不稳定进行量身定制的治疗干预。