Infantile spasm: A review on the severity of epileptic encephalopathy

Sujithra Srinivas
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Abstract

Infantile spasm (IS) comprises of both an age dependent epileptic seizure and distinctive seizure Onset in infants. In the recent past the key observation in classification and standardization of infantile spasm has culminated many recommendations in distinguishing and recognizing the seizure type and the epileptic syndrome or the West syndrome. The Infantile spasm is an early onset epileptic encephalopathy which presents unique electrographic and clinical features, these features are found in children in the middle of the first year of their birth .However the pathophysiology and the heterogeneity of the infantile spasm remains partially or incompletely understood. In the neurobiological basis there are multiple aetiologies converge to form similar clinical interpretations. The description of the electroencephalographic features of the spasm and its hypsarrthythmia plays a pivot role in early diagnosis. The treatment options for infantile spasm are very limited and it is also called a “catastrophic” due to the poor developmental, cognitive and epileptic progress. In the recent past more detailed information about the electrographic and clinical features of the spasms and hypsarrhythmia in EEG has emerged. The advances in the neuro imaging techniques have revealed about the aetiology and the pathophysiology of infantile spasm to yield a prognosis in patients with infantile spasms. The pathophysiology of infantile spasm needs to be better clarified for any kind of novel treatments and a wide range of preclinical animal studies are essential for advancing the knowledge. Here, in this review paper we focus on the preclinical models of Infantile spasm, with information’s regarding the existing models and research findings, elaborate on some novel models and discuss on new data that can help in advancing the understanding of the cellular mechanisms underlying the specific EEG changes such as ictal electrodecrement and interictal hypsarrhythmia presented in Infantile spasm IS.
婴儿痉挛:癫痫性脑病严重程度的综述
婴儿痉挛(IS)包括年龄依赖性癫痫发作和婴儿独特的癫痫发作。近年来,对小儿痉挛的分类和标准化进行了重点观察,并提出了许多区分和识别癫痫发作类型和癫痫综合征或西综合征的建议。婴儿痉挛是一种早期发作的癫痫性脑病,具有独特的电图和临床特征,这些特征在出生第一年中期的儿童中发现。然而,婴儿痉挛的病理生理学和异质性仍然部分或不完全了解。在神经生物学基础上,有多种病因汇聚形成类似的临床解释。痉挛的脑电图特征及其心律失常的描述在早期诊断中起着关键作用。婴儿痉挛的治疗选择非常有限,由于发育不良,认知和癫痫进展,它也被称为“灾难性的”。近年来,关于脑电图痉挛和心律失常的电图和临床特征的详细信息已经出现。神经影像学技术的进步已经揭示了婴儿痉挛的病因和病理生理学,从而对婴儿痉挛患者的预后产生影响。婴儿痉挛的病理生理学需要更好地阐明任何一种新的治疗方法,广泛的临床前动物研究对于推进这方面的知识至关重要。在本文中,我们重点介绍了婴儿痉挛的临床前模型,介绍了现有模型和研究成果,阐述了一些新的模型,并讨论了一些新的数据,这些数据可以帮助我们更好地理解婴儿痉挛IS中出现的特定脑电图变化(如初始电减量和间期心律失常)的细胞机制。
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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