Ademuwagun Ibitayo Abigail, Rotimi Solomon Oladapo, Syrbe Steffen, Ajamma Yvonne Ukamaka, Adebiyi Ezekiel
Covenant University Bioinformatics Research, Covenant University, Ota, Nigeria.
Department of Biochemistry, Covenant University, Ota, Nigeria.
Front Neurol. 2021 Mar 24;12:600050. doi: 10.3389/fneur.2021.600050. eCollection 2021.
Genetic epilepsy occurs as a result of mutations in either a single gene or an interplay of different genes. These mutations have been detected in ion channel and non-ion channel genes. A noteworthy class of ion channel genes are the voltage gated sodium channels (VGSCs) that play key roles in the depolarization phase of action potentials in neurons. Of huge significance are , and genes that are highly expressed in the brain. Genomic studies have revealed inherited and mutations in sodium channels that are linked to different forms of epilepsies. Due to the high frequency of sodium channel mutations in epilepsy, this review discusses the pathogenic mutations in the sodium channel genes that lead to epilepsy. In addition, it explores the functional studies on some known mutations and the clinical significance of VGSC mutations in the medical management of epilepsy. The understanding of these channel mutations may serve as a strong guide in making effective treatment decisions in patient management.
遗传性癫痫是由单个基因的突变或不同基因之间的相互作用引起的。这些突变已在离子通道基因和非离子通道基因中被检测到。一类值得注意的离子通道基因是电压门控钠通道(VGSCs),它们在神经元动作电位的去极化阶段起着关键作用。在大脑中高度表达的基因具有极其重要的意义。基因组研究已经揭示了与不同形式癫痫相关的钠通道的遗传和突变。由于癫痫中钠通道突变的频率很高,本综述讨论了导致癫痫的钠通道基因中的致病突变。此外,它还探讨了对一些已知突变的功能研究以及VGSC突变在癫痫医学管理中的临床意义。对这些通道突变的理解可能会为患者管理中的有效治疗决策提供有力指导。