作为 SOZ 定位生物标志物的高频爆发的连接性。

Frontiers in network physiology Pub Date : 2024-09-20 eCollection Date: 2024-01-01 DOI:10.3389/fnetp.2024.1441998
Marco Pinto-Orellana, Beth Lopour
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引用次数: 0

摘要

对于难治性癫痫患者来说,癫痫发作起始区(SOZ)在确定手术切除的特定脑区方面起着至关重要的作用。高频振荡(HFO)和基于连接的方法已被确定为定位癫痫发作区的潜在生物标志物。然而,对于如何估算高频振荡事件之间的连通性,以及针对特定受试者的短期可靠性,目前还没有达成共识。因此,我们提出用通道级连通性离散度(CLCD)来量化单个电极间同步的变异性,并识别同步异常的电极群,我们假设这些电极群与 SOZ 相关。此外,我们还开发了一种专门的滤波方法,可以减少因滤波宽带伪影(如尖锐瞬变、尖峰或直流偏移)而引起的振荡成分。因此,我们的连通性估计值对这些波形的存在具有稳健性。为了计算我们的指标,我们首先创建二进制信号,指示每个通道中是否存在高频突变,并据此计算通道之间的成对连通性。然后,通过组合连通性矩阵和测量每个电极的组合连通性值的变异性来计算 CLCD。我们使用两个独立的开放存取数据集测试了我们的方法,这两个数据集分别包含 89 名和 15 名难治性癫痫患者的颅内脑电图信号。这些数据集中的记录以大约 1000 Hz 的频率采样,我们提出的 CLCD 是在波纹带(80-200 Hz)进行估算的。在第一个数据集中,所有患者的平均 ROC-AUC 为 0.73,平均 Cohen's d 为 1.05,而在第二个数据集中,平均 ROC-AUC 为 0.78,Cohen's d 为 1.07。平均而言,SOZ 信道的 CLCD 值低于非 SOZ 信道。此外,基于第二个数据集(包括手术结果(Engel I-IV)),我们的分析表明,较高的 CLCD 四分位数(作为 CLCD 分布散布的度量)与良好的结果(Engel I)相关。这表明,CLCD 可显著帮助识别 SOZ 群,从而为癫痫患者的手术规划提供额外的工具。
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Connectivity of high-frequency bursts as SOZ localization biomarker.

For patients with refractory epilepsy, the seizure onset zone (SOZ) plays an essential role in determining the specific regions of the brain that will be surgically resected. High-frequency oscillations (HFOs) and connectivity-based approaches have been identified among the potential biomarkers to localize the SOZ. However, there is no consensus on how connectivity between HFO events should be estimated, nor on its subject-specific short-term reliability. Therefore, we propose the channel-level connectivity dispersion (CLCD) as a metric to quantify the variability in synchronization between individual electrodes and to identify clusters of electrodes with abnormal synchronization, which we hypothesize to be associated with the SOZ. In addition, we developed a specialized filtering method that reduces oscillatory components caused by filtering broadband artifacts, such as sharp transients, spikes, or direct current shifts. Our connectivity estimates are therefore robust to the presence of these waveforms. To calculate our metric, we start by creating binary signals indicating the presence of high-frequency bursts in each channel, from which we calculate the pairwise connectivity between channels. Then, the CLCD is calculated by combining the connectivity matrices and measuring the variability in each electrode's combined connectivity values. We test our method using two independent open-access datasets comprising intracranial electroencephalography signals from 89 to 15 patients with refractory epilepsy, respectively. Recordings in these datasets were sampled at approximately 1000 Hz, and our proposed CLCDs were estimated in the ripple band (80-200 Hz). Across all patients in the first dataset, the average ROC-AUC was 0.73, and the average Cohen's d was 1.05, while in the second dataset, the average ROC-AUC was 0.78 and Cohen's d was 1.07. On average, SOZ channels had lower CLCD values than non-SOZ channels. Furthermore, based on the second dataset, which includes surgical outcomes (Engel I-IV), our analysis suggested that higher CLCD interquartile (as a measure of CLCD distribution spread) is associated with favorable outcomes (Engel I). This suggests that CLCD could significantly assist in identifying SOZ clusters and, therefore, provide an additional tool in surgical planning for epilepsy patients.

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