{"title":"Characterizing Higher-order Functional Brain Networks with Simplicial Complexes and Temporal Dynamics.","authors":"Xinyu Li, Pengyu Cheng, Chenlong Wang, Yunlu Cai, Jiaying Yan, Zhaohui Li, Xi Zhang","doi":"10.1109/TBME.2026.3737173","DOIUrl":null,"url":null,"abstract":"<p><p>While conventional approaches characterize brain functional connectivity using static, pairwise interactions, higher-order interactions among multiple regions and their temporal organization are also essential for understanding complex brain dynamics. Here, we propose a temporal higher-order functional brain network framework (THFBN) that integrates simplicial complexes with temporal dynamical modeling to infer directed, time-varying higher-order interactions from stereoelectroencephalography (SEEG) recordings in epilepsy. We show that higher-order interactions across time reveals structured network reconfigurations that are not captured by static higher-order representations alone, giving rise to rapid yet structured network reconfigurations that are not captured by static or pairwise representations. Applying THFBN to epileptic seizures reveals a spatially heterogeneous redistribution of higher-order positive and negative predictive influences across seizure stages, with the strongest variability observed in temporal and insular regions, while positive-negative balance remains generally stable despite substantial changes in influence strength. Together, these findings demonstrate that integrating temporal dynamics with higher-order interactions reveals structured network reconfigurations during seizure evolution that are not captured by conventional connectivity models, and provide a principled framework for studying dynamic higher-order brain organization in epilepsy.</p>","PeriodicalId":13245,"journal":{"name":"IEEE Transactions on Biomedical Engineering","volume":"PP ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2026-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Biomedical Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1109/TBME.2026.3737173","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
While conventional approaches characterize brain functional connectivity using static, pairwise interactions, higher-order interactions among multiple regions and their temporal organization are also essential for understanding complex brain dynamics. Here, we propose a temporal higher-order functional brain network framework (THFBN) that integrates simplicial complexes with temporal dynamical modeling to infer directed, time-varying higher-order interactions from stereoelectroencephalography (SEEG) recordings in epilepsy. We show that higher-order interactions across time reveals structured network reconfigurations that are not captured by static higher-order representations alone, giving rise to rapid yet structured network reconfigurations that are not captured by static or pairwise representations. Applying THFBN to epileptic seizures reveals a spatially heterogeneous redistribution of higher-order positive and negative predictive influences across seizure stages, with the strongest variability observed in temporal and insular regions, while positive-negative balance remains generally stable despite substantial changes in influence strength. Together, these findings demonstrate that integrating temporal dynamics with higher-order interactions reveals structured network reconfigurations during seizure evolution that are not captured by conventional connectivity models, and provide a principled framework for studying dynamic higher-order brain organization in epilepsy.
期刊介绍:
IEEE Transactions on Biomedical Engineering contains basic and applied papers dealing with biomedical engineering. Papers range from engineering development in methods and techniques with biomedical applications to experimental and clinical investigations with engineering contributions.