Department of Neurology, University of Minnesota, Minneapolis, United States of America.
Department of Neurology, University of Minnesota, Minneapolis, United States of America.
Neurobiol Dis. 2023 Jan;176:105963. doi: 10.1016/j.nbd.2022.105963. Epub 2022 Dec 12.
Excessive daytime sleepiness is a recognized non-motor symptom that adversely impacts the quality of life of people with Parkinson's disease (PD), yet effective treatment options remain limited. Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for PD motor signs. Reliable daytime sleep-wake classification using local field potentials (LFPs) recorded from DBS leads implanted in STN can inform the development of closed-loop DBS approaches for prompt detection and disruption of sleep-related neural oscillations. We performed STN DBS lead recordings in three nonhuman primates rendered parkinsonian by administrating neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). Reference sleep-wake states were determined on a second-by-second basis by video monitoring of eyes (eyes-open, wake and eyes-closed, sleep). The spectral power in delta (1-4 Hz), theta (4-8 Hz), low-beta (8-20 Hz), high-beta (20-35 Hz), gamma (35-90 Hz), and high-frequency (200-400 Hz) bands were extracted from each wake and sleep epochs for training (70% data) and testing (30% data) a support vector machines classifier for each subject independently. The spectral features yielded reasonable daytime sleep-wake classification (sensitivity: 90.68 ± 1.28; specificity: 88.16 ± 1.08; accuracy: 89.42 ± 0.68; positive predictive value; 88.70 ± 0.89, n = 3). Our findings support the plausibility of monitoring daytime sleep-wake states using DBS lead recordings. These results could have future clinical implications in informing the development of closed-loop DBS approaches for automatic detection and disruption of sleep-related neural oscillations in people with PD to promote wakefulness.
日间过度嗜睡是一种公认的非运动症状,会对帕金森病 (PD) 患者的生活质量产生不利影响,但有效的治疗选择仍然有限。丘脑底核 (STN) 的深部脑刺激 (DBS) 是治疗 PD 运动症状的有效方法。使用植入 STN 的 DBS 导联记录的局部场电位 (LFP) 进行可靠的日间睡眠-觉醒分类,可以为开发用于及时检测和中断与睡眠相关的神经振荡的闭环 DBS 方法提供信息。我们在通过施用神经毒素 1-甲基-4-苯基-1,2,3,6-四氢吡啶 (MPTP) 使三只非人类灵长类动物患上帕金森病后,对 STN 的 DBS 导联进行了记录。通过对眼睛(睁眼、清醒和闭眼、睡眠)的视频监控,逐秒确定参考睡眠-觉醒状态。从每个清醒和睡眠期提取 delta(1-4 Hz)、theta(4-8 Hz)、低β(8-20 Hz)、高β(20-35 Hz)、γ(35-90 Hz)和高频(200-400 Hz)频段的频谱功率,用于为每个受试者独立训练(70%的数据)和测试(30%的数据)支持向量机分类器。这些频谱特征产生了合理的日间睡眠-觉醒分类(灵敏度:90.68±1.28;特异性:88.16±1.08;准确性:89.42±0.68;阳性预测值;88.70±0.89,n=3)。我们的研究结果支持使用 DBS 导联记录监测日间睡眠-觉醒状态的合理性。这些结果可能对开发闭环 DBS 方法具有未来的临床意义,以便自动检测和中断 PD 患者与睡眠相关的神经振荡,从而促进觉醒。