Candidate Genes Associated with the Course of Epilepsy in Cerebral Palsy: Remission or Refractoriness

P. L. Sokolov, N. V. Chebanenko, D. M. Mednaya, Vladimir V. Arkhipov
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Abstract

Epilepsy often accompanies congenital cerebral palsy (CP). Canalopathies can be the cause of congenital epilepsy. The aim of the study is to determine the influence of various determinants on the course of epilepsy. Materials and methods: The results of clinical and genetic analysis of 136 cases of cerebral palsy (CP) with epilepsy are presented. The patients were divided into groups according to the syndromes according to the classification of CP (Panteliadis and R. Korinthenberg, 2005). Epileptic syndromes were divided into three groups: focal childhood epilepsy with structural brain changes and benign epileptiform discharges (BEDC) in EEG - 41 children (30.1%), structural focal epilepsy - 37 children (27.2%), epileptic encephalopathies 58 children (42.7%). Pathogenic variants in genes were confirmed by next generation sequencing (NGS) Sanger methods of venous blood. Results. Remission was more difficult to achieve in patients with determinants of regulation of general aspects of cellular metabolism, mitochondrial function, cytoskeleton formation and function, and transport across the outer membrane. The need for polypharmacy was in the groups that regulate the function of mitochondria, the formation and functioning of the cytoskeleton, and the regulation of membrane excitability. Conclusion. Determinant analysis provides a better understanding of the mechanisms of patient responsiveness to anticonvulsant therapy. The determinant of mitochondrial function most significantly affects its effectiveness. Probably, the violation of energy metabolism in the cell neutralizes the stabilization of the neuronal membrane under the influence of anticonvulsants. The determinant of the formation and functioning of the cytoskeleton, according to our preliminary data, is associated with the formation of malformations of the brain. In this case, the refractoriness of epilepsy can be secondary and determined by the severity of structural changes in the brain.
与脑瘫癫痫病程相关的候选基因:缓解还是难治
先天性脑瘫(CP)常伴有癫痫。胼胝体病可能是先天性癫痫的病因。本研究旨在确定各种决定因素对癫痫病程的影响。材料和方法本研究对 136 例伴有癫痫的脑性瘫痪(CP)患者进行了临床和遗传分析。根据 CP 分类法(Panteliadis 和 R. Korinthenberg,2005 年),按照综合征将患者分组。癫痫综合征分为三组:伴有脑结构改变和脑电图良性癫痫样放电(BEDC)的局灶性儿童癫痫--41 名儿童(30.1%)、结构性局灶性癫痫--37 名儿童(27.2%)、癫痫性脑病--58 名儿童(42.7%)。通过对静脉血进行下一代测序(NGS)桑格方法确认了基因中的致病变异。结果显示对细胞代谢、线粒体功能、细胞骨架的形成和功能以及跨外膜转运等一般方面有决定性调控因素的患者更难获得缓解。调节线粒体功能、细胞骨架的形成和功能以及膜兴奋性调节的组别需要多种药物治疗。结论决定因素分析有助于更好地了解患者对抗惊厥治疗反应性的机制。线粒体功能的决定因素对疗效影响最大。在抗惊厥药的影响下,细胞内能量代谢的破坏可能会中和神经元膜的稳定性。根据我们的初步数据,细胞骨架的形成和功能的决定因素与大脑畸形的形成有关。在这种情况下,癫痫的折射性可能是继发性的,由大脑结构变化的严重程度决定。
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