同性恋
透视图(图形)
计算机科学
单调函数
群(周期表)
理论(学习稳定性)
认知心理学
人工智能
选择(遗传算法)
赖特
心理学
癫痫
联轴节(管道)
机器学习
互惠的
计量经济学
价值(数学)
人工神经网络
理论计算机科学
点(几何)
一般化
连接体
社会心理学
模式识别(心理学)
数学
点过程
统计物理学
功能连接
资源(消歧)
作者
Zhaohui Li,Yunlu Cai,Weina Cai,Xin Jin,Xinyu Li,Zhang Xi
标识
DOI:10.1088/1741-2552/ae1ea0
摘要
Abstract Objective. Group interactions capture cooperative dynamics among neural populations quantitatively, while also enabling precise detection of ensemble-level synchrony patterns and transcending the limitations of node-level relationships. To evaluate higher-order group interactions, we propose the PLASSO-homophily framework using multichannel stereo-electroencephalography (SEEG) recorded from patients with epilepsy. Approach. Specifically, we use phase locking value to improve least absolute shrinkage and selection operator method for constructing hypergraphs. Afterwards, we calculate affinity ratios between brain zones. Finally, we investigate higher-order interactions among different groups from a homophily perspective. The extremal result of strict homophily serves as a crucial theoretical framework for understanding homophily concepts, reflecting the constraints that different groups follow in higher-order interactions. Main results. It is observed that group interactions between seizure onset zones (SOZ), propagation zones (PZ) and non-involved zones (NIZ) present significant distinction across different seizure phases. In particular, the homophily of SOZ reaches a peak point during the seizure and sharply decreases in the post-seizure, with the most statistically significant differences on θ and γ bands. Furthermore, during the seizure, SOZ-PZ exhibits enhanced coupling while SOZ-NIZ exhibits impaired functional integration. Finally, among three groups, only SOZ exhibits strict monotonic and majority homophily. Significance. By analyzing changes in in-class and out-class connectivity, we quantitatively assess the activity levels and combinatorial constraints of the SOZ, PZ, and NIZ, thereby providing a novel perspective for exploring seizure mechanisms and developing epilepsy treatments.
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