Duncan Dominique, Vespa Paul, Toga Arthur W
USC Stevens Neuroimaging and Informatics Institute, University of Southern California, 2025 Zonal Ave, Los Angeles, CA, 90033, USA.
Division of Neurosurgery and Department of Neurology, University of California at Los Angeles School of Medicine, 10833 LeConte Avenue, CHS 18-218, Los Angeles, CA, 90024, USA and USC Stevens Neuroimaging and Informatics Institute, University of Southern California, 2025 Zonal Ave, Los Angeles, CA, 90033, USA.
Discrete Continuous Dyn Syst Ser B. 2018 Jan;23(1):161-172. doi: 10.3934/dcdsb.2018010.
Epilepsy is among the most common serious disabling disorders of the brain, and the global burden of epilepsy exerts a tremendous cost to society. Most people with epilepsy have acquired forms, and the development of antiepileptogenic interventions could potentially prevent or cure these epilepsies [3, 13]. The discovery of potential antiepileptogenic treatments is currently a high research priority. Clinical validation would require a means to identify populations of patients at particular high risk for epilepsy after a potential epileptogenic insult to know when to treat and to document prevention or cure. We investigate the development of post-traumatic epilepsy (PTE) following traumatic brain injury (TBI), because this condition offers the best opportunity to know the time of onset of epileptogenesis in patients. Epileptogenesis is common after TBI, and because much is known about the physical history of PTE, it represents a near-ideal human model in which to study the process of developing seizures. Using scalp and depth EEG recordings for six patients, the goal of our analysis is to find a way to quantitatively detect features in the EEG that could potentially help predict seizure onset post trauma. Unsupervised Diffusion Component Analysis [5], a novel approach based on the diffusion mapping framework [4], reduces data dimensionality and provides pattern recognition that can be used to distinguish different states of the patient, such as seizures and non-seizure spikes in the EEG. This method is also adapted to the data to enable the extraction of the underlying brain activity. Previous work has shown that such techniques can be useful for seizure prediction [6]. Some new results that demonstrate how this algorithm is used to detect spikes in the EEG data as well as other changes over time are shown. This nonlinear and local network approach has been used to determine if the early occurrences of specific electrical features of epileptogenesis, such as interictal epileptiform activity and morphologic changes in spikes and seizures, during the initial week after TBI predicts the development of PTE.
癫痫是最常见的严重致残性脑部疾病之一,癫痫的全球负担给社会带来了巨大成本。大多数癫痫患者为后天获得性癫痫,抗癫痫发生干预措施的研发有可能预防或治愈这些癫痫[3, 13]。发现潜在的抗癫痫发生治疗方法是当前的一项高度优先研究课题。临床验证需要一种方法来识别在遭受潜在致痫性损伤后癫痫发作风险特别高的患者群体,以便知道何时进行治疗并记录预防或治愈情况。我们研究创伤性脑损伤(TBI)后创伤后癫痫(PTE)的发生情况,因为这种情况为了解患者癫痫发生的起始时间提供了最佳机会。癫痫发生在TBI后很常见,而且由于对PTE的病史了解很多,它代表了一个近乎理想的人类模型,可用于研究癫痫发作的发展过程。我们对6名患者进行头皮和深部脑电图记录,分析的目标是找到一种方法来定量检测脑电图中的特征,这些特征可能有助于预测创伤后癫痫发作的起始。无监督扩散成分分析[5]是一种基于扩散映射框架[4]的新方法,可降低数据维度并提供模式识别,用于区分患者的不同状态,如脑电图中的癫痫发作和非癫痫发作尖峰。该方法还适用于数据,以提取潜在的脑活动。先前的研究表明,此类技术可用于癫痫发作预测[6]。展示了一些新结果,这些结果说明了该算法如何用于检测脑电图数据中的尖峰以及随时间的其他变化。这种非线性和局部网络方法已被用于确定TBI后第一周内癫痫发生的特定电特征(如发作间期癫痫样活动以及尖峰和癫痫发作的形态变化)的早期出现是否可预测PTE的发展。