The interictal suppression hypothesis is the dominant differentiator of seizure onset zones in focal epilepsy.

IF 10.6 1区 医学 Q1 CLINICAL NEUROLOGY
Brain Pub Date : 2024-09-03 DOI:10.1093/brain/awae189
Derek J Doss, Jared S Shless, Sarah K Bick, Ghassan S Makhoul, Aarushi S Negi, Camden E Bibro, Rohan Rashingkar, Abhijeet Gummadavelli, Catie Chang, Martin J Gallagher, Robert P Naftel, Shilpa B Reddy, Shawniqua Williams Roberson, Victoria L Morgan, Graham W Johnson, Dario J Englot
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Abstract

Successful surgical treatment of drug-resistant epilepsy traditionally relies on the identification of seizure onset zones (SOZs). Connectome-based analyses of electrographic data from stereo electroencephalography (SEEG) may empower improved detection of SOZs. Specifically, connectome-based analyses based on the interictal suppression hypothesis posit that when the patient is not having a seizure, SOZs are inhibited by non-SOZs through high inward connectivity and low outward connectivity. However, it is not clear whether there are other motifs that can better identify potential SOZs. Thus, we sought to use unsupervised machine learning to identify network motifs that elucidate SOZs and investigate if there is another motif that outperforms the ISH. Resting-state SEEG data from 81 patients with drug-resistant epilepsy undergoing a pre-surgical evaluation at Vanderbilt University Medical Center were collected. Directed connectivity matrices were computed using the alpha band (8-13 Hz). Principal component analysis (PCA) was performed on each patient's connectivity matrix. Each patient's components were analysed qualitatively to identify common patterns across patients. A quantitative definition was then used to identify the component that most closely matched the observed pattern in each patient. A motif characteristic of the interictal suppression hypothesis (high-inward and low-outward connectivity) was present in all individuals and found to be the most robust motif for identification of SOZs in 64/81 (79%) patients. This principal component demonstrated significant differences in SOZs compared to non-SOZs. While other motifs for identifying SOZs were present in other patients, they differed for each patient, suggesting that seizure networks are patient specific, but the ISH is present in nearly all networks. We discovered that a potentially suppressive motif based on the interictal suppression hypothesis was present in all patients, and it was the most robust motif for SOZs in 79% of patients. Each patient had additional motifs that further characterized SOZs, but these motifs were not common across all patients. This work has the potential to augment clinical identification of SOZs to improve epilepsy treatment.

发作间期抑制假说是区分局灶性癫痫发作起始区的主要依据。
耐药性癫痫的成功手术治疗传统上依赖于癫痫发作区(SOZ)的识别。对来自立体脑电图(SEEG)的电图数据进行基于连接体的分析,可提高对 SOZ 的检测能力。具体来说,基于发作间期抑制假说(ISH)的连接组分析认为,当患者没有癫痫发作时,SOZ 会通过高内向连接性和低外向连接性受到非 SOZ 的抑制。然而,目前还不清楚是否有其他主题能更好地识别潜在的 SOZ。因此,我们试图利用无监督机器学习来识别能阐明 SOZ 的网络图案,并研究是否有其他图案优于 ISH。我们收集了范德比尔特大学医学中心 81 名接受手术前评估的耐药性癫痫患者的静息态 SEEG 数据。利用α波段(8-12Hz)计算了定向连接矩阵。对每位患者的连接矩阵进行了主成分分析(PCA)。对每位患者的成分进行定性分析,以确定不同患者的共同模式。然后使用定量定义来确定与每位患者观察到的模式最匹配的成分。发作间期抑制假说(高内向和低外向连通性)的特征图案在所有患者中都存在,并且在 64/81 例(79%)患者中被发现是用于识别 SOZ 的最稳健图案。与非 SOZ 相比,该主成分在 SOZ 中显示出显著差异。虽然用于识别 SOZ 的其他主成分也存在于其他患者中,但每个患者的情况各不相同,这表明癫痫发作网络具有患者特异性,但 ISH 几乎存在于所有网络中。我们发现,基于发作间期抑制假说的潜在抑制基团存在于所有患者中,而且在 79% 的患者中,它是 SOZs 最稳健的基团。每名患者都有进一步描述 SOZs 特征的其他基调,但这些基调在所有患者中并不常见。这项工作有可能增强SOZ的临床识别能力,从而改善癫痫治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
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