Structural network-specific effect of extreme capsule stimulation for drug-resistant focal epilepsy.

IF 11.7 1区 医学 Q1 CLINICAL NEUROLOGY Brain Pub Date : 2025-08-01 DOI:10.1093/brain/awaf097
Yueyang Cheng, Di Wang, Xiaohua Zhang, Guangyuan Jin, Di Wu, Qiao Wang, Jialin Du, Lei Qi, Cuiping Xu, Zichen Qiao, Xiaopeng Wang, Junliang Ge, Siyi Wang, Hao Yan, Xueyuan Wang, Huaqiang Zhang, Tao Yu, Yuping Wang, Fang-Cheng Yeh, Guoguang Zhao, Liankun Ren
{"title":"Structural network-specific effect of extreme capsule stimulation for drug-resistant focal epilepsy.","authors":"Yueyang Cheng, Di Wang, Xiaohua Zhang, Guangyuan Jin, Di Wu, Qiao Wang, Jialin Du, Lei Qi, Cuiping Xu, Zichen Qiao, Xiaopeng Wang, Junliang Ge, Siyi Wang, Hao Yan, Xueyuan Wang, Huaqiang Zhang, Tao Yu, Yuping Wang, Fang-Cheng Yeh, Guoguang Zhao, Liankun Ren","doi":"10.1093/brain/awaf097","DOIUrl":null,"url":null,"abstract":"<p><p>Treatment for drug-resistant epilepsy in poor candidates for resection surgeries remains challenging. The prevailing deep brain stimulation of subcortical nuclei is effective but exhibits heterogeneous efficacy and unpredictable side effects. Therefore, the investigation of novel deep brain stimulation targets is of paramount importance. Here, we focused on the unique structure known as the extreme capsule (EC), which is a 'butterfly'-like structure passing through the uncinate fasciculus, the inferior fronto-occipital fasciculus and the convergence of the short association fibres connecting to the insula. We investigated the modulatory effect of EC stimulation in 11 drug-resistant epilepsy patients (mean age, 28 years; eight males and three females) who underwent stereo-electroencephalography as part of presurgical evaluation. One electrode was extended to the EC ipsilateral to the presumed seizure onset zone. Structural connectivity to the EC derived from structural human connectome data (n = 1065) was estimated to compare with the effective connectivity to the EC using single-pulse stimulation at 1 Hz during the resting state. To assess the modulatory effect of EC stimulation, we used stepwise incremental stimulation ranging from 5 to 145 Hz in a cyclical pattern. We evaluated how neural activity across distributed cortical areas synchronized with EC stimulation frequencies, in addition to the changes in interictal epileptiform discharges and ripples during the stimulation period compared with the baseline. Moreover, 1 Hz burst stimulation mode was applied to refine the stimulation protocol further. We showed that the EC effective connectivity aligned well with the EC structural network. We also observed that the synchronized and desynchronized modulatory effect of EC stimulation was frequency specific across all the patients. Most importantly, we found that the modulatory effect of EC stimulation was constrained by its structural connectivity. Specifically, high-frequency stimulation of the EC significantly suppressed the epileptic discharges in the ipsilateral orbitofrontal lobe, occipital gyrus, inferior frontal gyrus, insula and temporal pole, which were inside the EC structural network rather than outside it (P < 0.001). Of note, EC 1 Hz burst stimulation demonstrated a comparable inhibitory efficacy to conventional high-frequency stimulation (ANOVA, F = 5.331, P < 0.001). This proof-of-concept study demonstrates that the EC is a promising deep brain stimulation target for treating substantial focal epilepsy with seizure originating from EC structurally connected cortex. It also demonstrates the feasibility of transforming knowledge of white matter node stimulation for seizures originating from its physically connected cortex and offers a promising therapeutic approach using alternative stimulation methods.</p>","PeriodicalId":9063,"journal":{"name":"Brain","volume":" ","pages":"2920-2934"},"PeriodicalIF":11.7000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/brain/awaf097","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Treatment for drug-resistant epilepsy in poor candidates for resection surgeries remains challenging. The prevailing deep brain stimulation of subcortical nuclei is effective but exhibits heterogeneous efficacy and unpredictable side effects. Therefore, the investigation of novel deep brain stimulation targets is of paramount importance. Here, we focused on the unique structure known as the extreme capsule (EC), which is a 'butterfly'-like structure passing through the uncinate fasciculus, the inferior fronto-occipital fasciculus and the convergence of the short association fibres connecting to the insula. We investigated the modulatory effect of EC stimulation in 11 drug-resistant epilepsy patients (mean age, 28 years; eight males and three females) who underwent stereo-electroencephalography as part of presurgical evaluation. One electrode was extended to the EC ipsilateral to the presumed seizure onset zone. Structural connectivity to the EC derived from structural human connectome data (n = 1065) was estimated to compare with the effective connectivity to the EC using single-pulse stimulation at 1 Hz during the resting state. To assess the modulatory effect of EC stimulation, we used stepwise incremental stimulation ranging from 5 to 145 Hz in a cyclical pattern. We evaluated how neural activity across distributed cortical areas synchronized with EC stimulation frequencies, in addition to the changes in interictal epileptiform discharges and ripples during the stimulation period compared with the baseline. Moreover, 1 Hz burst stimulation mode was applied to refine the stimulation protocol further. We showed that the EC effective connectivity aligned well with the EC structural network. We also observed that the synchronized and desynchronized modulatory effect of EC stimulation was frequency specific across all the patients. Most importantly, we found that the modulatory effect of EC stimulation was constrained by its structural connectivity. Specifically, high-frequency stimulation of the EC significantly suppressed the epileptic discharges in the ipsilateral orbitofrontal lobe, occipital gyrus, inferior frontal gyrus, insula and temporal pole, which were inside the EC structural network rather than outside it (P < 0.001). Of note, EC 1 Hz burst stimulation demonstrated a comparable inhibitory efficacy to conventional high-frequency stimulation (ANOVA, F = 5.331, P < 0.001). This proof-of-concept study demonstrates that the EC is a promising deep brain stimulation target for treating substantial focal epilepsy with seizure originating from EC structurally connected cortex. It also demonstrates the feasibility of transforming knowledge of white matter node stimulation for seizures originating from its physically connected cortex and offers a promising therapeutic approach using alternative stimulation methods.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
极端胶囊刺激对耐药局灶性癫痫的结构网络特异性效应。
治疗耐药癫痫的不良候选人切除手术仍然具有挑战性。目前流行的皮层下核深部脑刺激是有效的,但表现出不均匀的疗效和不可预测的副作用。因此,研究新的DBS靶点具有至关重要的意义。在这里,我们关注的是被称为极限囊(EC)的独特结构,它是一种“蝴蝶”状结构,穿过钩状束、额枕下束和连接岛叶的短联合纤维的会聚。我们对11例耐药癫痫患者(平均年龄28岁;男性:女性= 8:3)接受立体脑电图作为术前评估的一部分。一个电极延伸到假定癫痫发作区的EC同侧。从人类结构连接组数据(n=1065)得出的脑脊液的结构连通性估计与静息状态下使用1hz单脉冲刺激的脑脊液的有效连通性进行比较。为了评估电刺激的调制效果,我们采用了5 Hz至145 Hz的周期性逐步增量刺激。我们评估了分布皮质区域的神经活动如何与EC刺激频率同步,以及与基线相比,刺激期间癫痫样放电和波纹的间隔变化。此外,采用1hz突发刺激模式,进一步完善了刺激方案。结果表明,电导器的有效连通性与电导器的结构网络一致。我们进一步观察到,同步和非同步的电刺激调制效应在所有患者中都是频率特异性的。最重要的是,我们发现电刺激的调制效应受其结构连通性的限制。具体而言,高频刺激脑电图显著抑制同侧脑电图结构网络内的眶额叶、枕回、额下回、脑岛和颞极的癫痫放电(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Brain
Brain 医学-临床神经学
CiteScore
20.30
自引率
4.10%
发文量
458
审稿时长
3-6 weeks
期刊介绍: Brain, a journal focused on clinical neurology and translational neuroscience, has been publishing landmark papers since 1878. The journal aims to expand its scope by including studies that shed light on disease mechanisms and conducting innovative clinical trials for brain disorders. With a wide range of topics covered, the Editorial Board represents the international readership and diverse coverage of the journal. Accepted articles are promptly posted online, typically within a few weeks of acceptance. As of 2022, Brain holds an impressive impact factor of 14.5, according to the Journal Citation Reports.
期刊最新文献
Long non-coding RNA Carip loss alters parabrachial synapses and drives pain hypersensitivity. The use of animals in neuroscience research. Loss of REST associated with Alzheimer's disease pathology is ameliorated by NAD. Hippocampal growth and function are reduced in the newborn following fetal growth restriction BTK inhibition suppresses neuroinflammation and neurodegeneration in amyotrophic lateral sclerosis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1