难治性癫痫患者的脉管和丘脑前核内侧受累。

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2024-12-10 Epub Date: 2024-11-12 DOI:10.1212/WNL.0000000000210039
Ryan McGinn, Erica Leah Von Stein, Anjali Datta, Teresa Wu, Zoe Lusk, Spencer Nam, Manveer Dilts-Garcha, Robert S Fisher, Vivek Buch, Josef Parvizi
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引用次数: 0

摘要

背景和目的:针对丘脑前核(ANT)的深部脑刺激(DBS)已被证明能有效治疗一些药物难治性癫痫患者。然而,相对于其他丘脑核,癫痫发作是如何通过丘脑前核扩散的仍是未知数。本研究旨在通过同时记录 ANT 和脉络核 (PLV) 来研究它们在癫痫发作传播中的作用。我们的目标是确定 ANT 是否是人类丘脑中癫痫发作传播的主要部位,尤其是对于源于颞叶内侧的局灶性癫痫发作:在一项回顾性设计中,我们研究了难治性癫痫患者的脑电图和临床记录,这些患者被植入了跨皮层区域的立体电子脑电图(sEEG)电极,其中一些电极被延伸到丘脑的不同部位(即多部位丘脑记录)。我们从斯坦福综合癫痫中心选取了带有 ANT 和 PLV 电极的患者,并收集了有关发作起始区(通常是颞区)和丘脑 2 个部位的发作活动的时间和解剖信息:我们招募了 17 名成年患者(5 名女性,平均年龄 32 岁),同时记录同侧 ANT 和 PLV。所有患者的手术均安全无并发症。100%的患者在癫痫发作时丘脑受累(88%的患者同时受累于ANT和PLV,82%的患者首先受累于PLV)。在确诊为海马或杏仁发作的患者中,62%最初受累,100%随后受累于PLV核。只有31%的患者最初会扩散到ANT。所有从局灶到双侧的强直阵挛发作和大多数局灶性意识障碍发作均有 ANT 和 PLV 早期受累,并迅速扩散到对侧核团。我们在此报告的癫痫发作传播模式提供了有关 PLV 核在癫痫发作传播过程中的突出参与的见解。这可能会促使未来在更大的患者群中开展前瞻性工作,以了解丘脑传播如何预测切除/烧蚀手术的反应,或 DBS 的个性化(例如,用 PLV 代替或与 ANT 一起使用)是否能改善临床预后。
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Ictal Involvement of the Pulvinar and the Anterior Nucleus of the Thalamus in Patients With Refractory Epilepsy.

Background and objectives: Deep brain stimulation (DBS) targeting the anterior nucleus of the thalamus (ANT) has been shown to be effective in treating some patients with medically refractory epilepsy. However, it remains unknown how seizures spread through the ANT relative to other thalamic nuclei. This study aimed to investigate, through simultaneous recordings from both ANT and pulvinar (PLV) nucleus, their roles in seizure propagation. Our goal was to determine whether the ANT is the primary site of seizure propagation in the human thalamus, especially for focal seizure originating in the medial temporal lobe.

Methods: In a retrospective design, we studied EEGs and clinical notes of patients with refractory epilepsy who were implanted with stereo-EEG (sEEG) electrodes across cortical regions, some of which were extended to reach various sites of the thalamus (i.e., multisite thalamic recordings). We selected patients from the Stanford Comprehensive Epilepsy Center with both ANT and PLV electrodes and collected information about the timing and anatomy of seizure activity in the seizure onset zones, usually temporal, and the 2 thalamic sites.

Results: We recruited 17 (5 female, mean age 32 years) adult patients with simultaneous ipsilateral ANT and PLV recordings. In all patients, the procedure was safe without any complications. In 100% of patients, the thalamus was involved during seizures (in 88% both ANT and PLV and in 82% first the PLV). In patients with confirmed hippocampal or amygdalar onset seizures, 62% had initial involvement and 100% had subsequent involvement of the PLV nucleus. Only 31% showed initial propagation to ANT. All focal-to-bilateral tonic-clonic seizures and most of the focal impaired awareness seizures had early involvement of both ANT and PLV, with rapid spread to the contralateral nuclei.

Discussion: sEEG of thalamic nuclei simultaneously provides an opportunity to understand propagation patterns of seizures with respect to each thalamic subdivision at the individual level. The patterns of seizure propagation, as we report here, provide insights about the prominent involvement of the PLV nucleus during seizure propagation. This may motivate future prospective work in larger cohorts of patients to understand how thalamic propagation may predict response to resective/ablative surgery or whether personalization of DBS (for instance, PLV instead of, or together with, ANT) could improve clinical outcomes.

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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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