Kimoto Yuki, Tani Naoki, Emura Takuto, Matsuhashi Takahiro, Yamamoto Takuto, Fujita Yuya, Oshino Satoru, Hosomi Koichi, Khoo Hui Ming, Miura Shimpei, Fujinaga Takahiro, Yanagisawa Takufumi, Kishima Haruhiko
Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Institute for Advanced Co-Creation Studies, Osaka University, Osaka, Japan.
Front Hum Neurosci. 2024 Nov 13;18:1495272. doi: 10.3389/fnhum.2024.1495272. eCollection 2024.
Despite using beta oscillations within the subthalamic nucleus as a biomarker of akinesia or rigidity in Parkinson's disease, a specific biomarker for freezing of gait (FOG) remains unclear. Recently, scalp phase-amplitude coupling (PAC) measured through scalp electroencephalography (EEG) has emerged as a promising tool for analyzing brain function. In this study, we examined whether PAC could be a biomarker for FOG.
We enrolled 11 patients with Parkinson's disease and recorded scalp EEG in preparation for and during gait while simultaneously assessing motor function, including FOG. We investigated changes in cortical PAC during walking with and without FOG and examined its correlation with the postural instability and gait difficulty (PIGD) score.
Patient characteristics were as follows: mean age 59.1 ± 6.9 years, disease duration 13.9 ± 4.1 years, and seven men. Four trials were excluded from the analysis owing to artifacts. In the trials without FOG ( = 18), beta-gamma PAC in the sensorimotor area decreased during gait preparation ( = 0.011; linear mixed-effects model), which was not the case in trials with FOG ( = 6) ( = 0.64; linear mixed-effects model). Using a support vector machine, machine learning of PAC during preparation for walking predicted the presence of FOG with an accuracy of 71.2%. Conversely, PAC increased during walking in trials with FOG ( = 0.0042; linear mixed-effects model), and PAC 20 s after the start of walking was positively correlated with the PIGD score (correlation coefficient = 0.406, = 0.032; Pearson's rank correlation).
Beta-gamma PAC in the sensorimotor area during preparation for walking differs depending on the emergence of FOG. As gait symptoms worsened, beta-gamma PAC in the sensorimotor area during walking gradually increased. Cortical PAC may be a biomarker for FOG in Parkinson's disease and may lead to the development of strategies to prevent falls in the future.
尽管将丘脑底核内的β振荡用作帕金森病运动不能或强直的生物标志物,但步态冻结(FOG)的特定生物标志物仍不明确。最近,通过头皮脑电图(EEG)测量的头皮相位-振幅耦合(PAC)已成为分析脑功能的一种有前景的工具。在本研究中,我们检验了PAC是否可能是FOG的生物标志物。
我们招募了11例帕金森病患者,在准备步态和步态期间记录头皮EEG,同时评估运动功能,包括FOG。我们研究了有FOG和无FOG行走期间皮质PAC的变化,并检验其与姿势不稳和步态困难(PIGD)评分的相关性。
患者特征如下:平均年龄59.1±6.9岁,病程13.9±4.1年,男性7例。由于伪迹,4次试验被排除在分析之外。在无FOG的试验(n = 18)中,感觉运动区的β-γ PAC在步态准备期间降低(P = 0.011;线性混合效应模型),而在有FOG的试验(n = 6)中并非如此(P = 0.64;线性混合效应模型)。使用支持向量机,对步行准备期间PAC进行机器学习预测FOG的存在,准确率为71.2%。相反,在有FOG的试验中步行期间PAC增加(P = 0.0042;线性混合效应模型),步行开始20秒后的PAC与PIGD评分呈正相关(相关系数 = 0.406,P = 0.032;Pearson等级相关)。
步行准备期间感觉运动区的β-γ PAC因FOG的出现而不同。随着步态症状恶化,步行期间感觉运动区的β-γ PAC逐渐增加。皮质PAC可能是帕金森病中FOG的生物标志物,未来可能会导致预防跌倒策略的发展。