Ahn Seong-Ho, Jang Han Na, Kim Seeun, Kim Min-Jee, Yum Mi-Sun, Jeong Dong-Hwa
Department of Artificial Intelligence, The Catholic University of Korea, 43 Jibong-ro, Bucheon, 14662, Gyeonggi-do, Republic of Korea.
Department of Pediatrics, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.
Sci Rep. 2025 Mar 19;15(1):9490. doi: 10.1038/s41598-025-93385-8.
Infantile epileptic spasm syndrome (IESS) is characterized by clustered epileptic spasms and hypsarrhythmia on electroencephalography (EEG). This study aimed to investigate the temporal dynamics and dynamic synchronization of neural networks in IESS using EEG microstate analysis of interictal recordings from 49 healthy controls (HC) and 42 patients with IESS. Five microstate maps were identified, and features including the global explained variance (GEV), mean correlation, occurrence, time coverage, mean time duration, and transition probabilities were extracted. Significant differences were observed in patients with IESS compared to HCs, with increased microstate features and transition probabilities in microstates A and B, and reduced values in microstates D and E. Furthermore, in patients with structural/metabolic etiologies, microstate A demonstrated heightened microstate features and transition probabilities compared to genetic/unknown etiologies. These microstate characteristics enabled accurate classification of IESS versus HCs and differentiation between structural/metabolic and genetic/unknown etiologies. The altered microstate topologies in IESS reflect disruptions in brain network dynamics, suggesting that specific microstate features and transition probabilities could serve as potential diagnostic biomarkers. This study underscores the potential of EEG microstate analysis in understanding neural dysfunction, particularly in structural/metabolic subtypes of IESS.
婴儿痉挛症综合征(IESS)的特征是癫痫痉挛成簇发作,脑电图(EEG)显示高峰失律。本研究旨在通过对49名健康对照(HC)和42名IESS患者的发作间期记录进行EEG微状态分析,研究IESS神经网络的时间动态和动态同步性。识别出五个微状态图,并提取了包括全局解释方差(GEV)、平均相关性、发生率、时间覆盖率、平均持续时间和转移概率等特征。与HC相比,IESS患者存在显著差异,微状态A和B的微状态特征和转移概率增加,而微状态D和E的值降低。此外,在具有结构/代谢病因的患者中,与遗传/未知病因相比,微状态A表现出更高的微状态特征和转移概率。这些微状态特征能够准确区分IESS与HC,并区分结构/代谢病因和遗传/未知病因。IESS中微状态拓扑结构的改变反映了脑网络动力学的破坏,表明特定的微状态特征和转移概率可作为潜在的诊断生物标志物。本研究强调了EEG微状态分析在理解神经功能障碍方面的潜力,特别是在IESS的结构/代谢亚型中。