{"title":"Inducing Long-Term Plastic Changes and Visual Attention Enhancement Via One-Week Cerebellar Crus II Intermittent Theta Burst Stimulation (iTBS): An EEG Study.","authors":"Meiliang Liu, Chao Yu, Minjie Tian, Jingping Shi, Yunfang Xu, Zijin Li, Zhengye Si, Xiaoxiao Yang, Xinyue Yang, Junhao Huang, Li Yao, Kuiying Yin, Zhiwen Zhao","doi":"10.1109/JBHI.2025.3551698","DOIUrl":null,"url":null,"abstract":"<p><p>Intermittent theta burst stimulation (iTBS) is a non-invasive technique frequently employed to induce neural plastic changes and enhance visual attention. Currently, most studies utilized a single iTBS session on healthy subjects to induce short-term neural plastic changes within tens of minutes post-stimulation and investigate its single-session effect on attention performance. Few studies have conducted multiple iTBS sessions on the cerebellum to explore long-term effects on the cerebral cortex and daily effects on visual attention performance. In this study, 18 healthy subjects were involved in a randomized, sham-controlled experiment over one week. All the subjects received daily session of bilateral cerebellar Crus II iTBS or sham stimulation and completed a visual search task. Resting-state electroencephalogram (EEG) was collected 48 hours pre- and post-experiment to assess plastic changes induced by iTBS. The results indicated that the iTBS group exhibited higher accuracy and lower time costs than the sham group after three sessions of iTBS. In addition, iTBS-induced plastic changes persisted up to 48 hours post-experiment, including left-shifted individual alpha frequency, increased intrinsic excitability (the likelihood that a neuron will generate an output in response to a given input), and enhanced PLV functional connectivity (phase synchronization between different brain region). Furthermore, we found that cerebellar iTBS induced a remote effect on the frontal region. Our study revealed the capacity of cerebellar Crus II iTBS to induce plastic changes and enhance attention performance, providing a potential avenue for using iTBS to promote rehabilitation.</p>","PeriodicalId":13073,"journal":{"name":"IEEE Journal of Biomedical and Health Informatics","volume":"PP ","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Journal of Biomedical and Health Informatics","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1109/JBHI.2025.3551698","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INFORMATION SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Intermittent theta burst stimulation (iTBS) is a non-invasive technique frequently employed to induce neural plastic changes and enhance visual attention. Currently, most studies utilized a single iTBS session on healthy subjects to induce short-term neural plastic changes within tens of minutes post-stimulation and investigate its single-session effect on attention performance. Few studies have conducted multiple iTBS sessions on the cerebellum to explore long-term effects on the cerebral cortex and daily effects on visual attention performance. In this study, 18 healthy subjects were involved in a randomized, sham-controlled experiment over one week. All the subjects received daily session of bilateral cerebellar Crus II iTBS or sham stimulation and completed a visual search task. Resting-state electroencephalogram (EEG) was collected 48 hours pre- and post-experiment to assess plastic changes induced by iTBS. The results indicated that the iTBS group exhibited higher accuracy and lower time costs than the sham group after three sessions of iTBS. In addition, iTBS-induced plastic changes persisted up to 48 hours post-experiment, including left-shifted individual alpha frequency, increased intrinsic excitability (the likelihood that a neuron will generate an output in response to a given input), and enhanced PLV functional connectivity (phase synchronization between different brain region). Furthermore, we found that cerebellar iTBS induced a remote effect on the frontal region. Our study revealed the capacity of cerebellar Crus II iTBS to induce plastic changes and enhance attention performance, providing a potential avenue for using iTBS to promote rehabilitation.
期刊介绍:
IEEE Journal of Biomedical and Health Informatics publishes original papers presenting recent advances where information and communication technologies intersect with health, healthcare, life sciences, and biomedicine. Topics include acquisition, transmission, storage, retrieval, management, and analysis of biomedical and health information. The journal covers applications of information technologies in healthcare, patient monitoring, preventive care, early disease diagnosis, therapy discovery, and personalized treatment protocols. It explores electronic medical and health records, clinical information systems, decision support systems, medical and biological imaging informatics, wearable systems, body area/sensor networks, and more. Integration-related topics like interoperability, evidence-based medicine, and secure patient data are also addressed.