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皮质发育畸形为何会引发癫痫。

Why Malformations of Cortical Development Cause Epilepsy.

作者信息

Represa Alfonso

机构信息

INSERM, Institut de Neurobiologie de la Méditerranée, Aix-Marseille University, Marseille, France.

出版信息

Front Neurosci. 2019 Mar 29;13:250. doi: 10.3389/fnins.2019.00250. eCollection 2019.

Abstract

Malformations of cortical development (MCDs), a complex family of rare disorders, result from alterations of one or combined developmental steps, including progenitors proliferation, neuronal migration and differentiation. They are an important cause of childhood epilepsy and frequently associate cognitive deficits and behavioral alterations. Though the physiopathological mechanisms of epilepsy in MCD patients remain poorly elucidated, research during the past decade highlighted the contribution of some factors that will be reviewed in this paper and that include: (i) the genes that caused the malformation, that can be responsible for a significant reduction of inhibitory cells (e.g., ARX gene) or be inducing cell-autonomous epileptogenic changes in affected neurons (e.g., mutations on the mTOR pathway); (ii) the alteration of cortical networks development induced by the malformation that will also involve adjacent or distal cortical areas apparently sane so that the epileptogenic focus might be more extended that the malformation or even localized at distance from it; (iii) the normal developmental processes that would influence and determine the onset of epilepsy in MCD patients, particularly precocious in most of the cases.

摘要

皮质发育畸形(MCDs)是一类复杂的罕见疾病,由一个或多个发育步骤的改变引起,包括祖细胞增殖、神经元迁移和分化。它们是儿童癫痫的重要病因,常伴有认知缺陷和行为改变。尽管MCD患者癫痫的生理病理机制仍未完全阐明,但过去十年的研究突出了一些因素的作用,本文将对此进行综述,这些因素包括:(i)导致畸形的基因,它们可能导致抑制性细胞显著减少(例如ARX基因),或在受影响的神经元中诱导细胞自主性致痫变化(例如mTOR通路的突变);(ii)畸形引起的皮质网络发育改变,这也会涉及相邻或远处看似正常的皮质区域,因此致痫灶可能比畸形范围更广,甚至位于远离畸形的部位;(iii)正常的发育过程,这些过程会影响并决定MCD患者癫痫的发作,在大多数情况下发作较早。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee04/6450262/719a9f118b3e/fnins-13-00250-g001.jpg

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