Academic Unit of Neurology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, University of Dublin, Room 5.43, 152-160 Pearse Street, Dublin 2, D02 R590, Ireland.
Department of Neurology, University Medical Centre Utrecht Brain Centre, Utrecht University, Utrecht, 3584 CG, The Netherlands.
Brain Topogr. 2024 Oct 4;38(1):3. doi: 10.1007/s10548-024-01078-8.
Amyotrophic lateral sclerosis (ALS) is characterised primarily by motor system degeneration, with clinical evidence of cognitive and behavioural change in up to 50% of cases. We have shown previously that resting-state EEG captures dysfunction in motor and cognitive networks in ALS. However, the longitudinal development of these dysfunctional patterns, especially in networks linked with cognitive-behavioural functions, remains unclear. Longitudinal studies on non-motor changes in ALS are essential to further develop our understanding of disease progression, improve care and enhance the evaluation of new treatments. To address this gap, we examined 124 ALS individuals with 128-channel resting-state EEG recordings, categorised by cognitive impairment (ALSci, n = 25), behavioural impairment (ALSbi, n = 58), or non-impaired (ALSncbi, n = 53), with 12 participants meeting the criteria for both ALSci and ALSbi. Using linear mixed-effects models, we characterised the general and phenotype-specific longitudinal changes in brain network, and their association with cognitive performance, behaviour changes, fine motor symptoms, and survival. Our findings revealed a significant decline in [Formula: see text]-band spectral power over time in the temporal region along with increased [Formula: see text]-band power in the fronto-temporal region in the ALS group. ALSncbi participants showed widespread β-band synchrony decrease, while ALSci participants exhibited increased co-modulation correlated with verbal fluency decline. Longitudinal network-level changes were specific of ALS subgroups and correlated with motor, cognitive, and behavioural decline, as well as with survival. Spectral EEG measures can longitudinally track abnormal network patterns, serving as a candidate stratification tool for clinical trials and personalised treatments in ALS.
肌萎缩侧索硬化症(ALS)主要表现为运动系统退化,多达 50%的病例有认知和行为改变的临床证据。我们之前已经表明,静息状态 EEG 可以捕捉到 ALS 中运动和认知网络的功能障碍。然而,这些功能障碍模式的纵向发展,特别是与认知行为功能相关的网络,仍然不清楚。ALS 中非运动变化的纵向研究对于进一步了解疾病进展、改善护理和增强新治疗方法的评估至关重要。为了弥补这一空白,我们检查了 124 名 ALS 个体的 128 通道静息状态 EEG 记录,根据认知障碍(ALSci,n=25)、行为障碍(ALSbi,n=58)或无损伤(ALSncbi,n=53)进行分类,其中 12 名参与者符合 ALSci 和 ALSbi 的标准。使用线性混合效应模型,我们描述了脑网络的一般和表型特异性纵向变化,以及它们与认知表现、行为变化、精细运动症状和生存的关系。我们的研究结果表明,随着时间的推移,ALS 组颞区的[Formula: see text]频带光谱功率显著下降,额颞区的[Formula: see text]频带功率增加。ALSncbi 参与者表现出广泛的β频带同步性下降,而 ALSci 参与者则表现出与言语流畅性下降相关的增加的共调制。纵向网络水平的变化是 ALS 亚组的特异性,并与运动、认知和行为下降以及生存相关。光谱 EEG 测量可以纵向跟踪异常网络模式,作为 ALS 临床试验和个性化治疗的候选分层工具。