Rubboli Guido, Gardella Elena, Cantalupo Gaetano, Alberto Tassinari Carlo
Danish Epilepsy Center, member of ERN EpiCARE, Kolonivej 1, 4293 Dianalund, Denmark; Institute of Clinical Medicine, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark.
Danish Epilepsy Center, member of ERN EpiCARE, Kolonivej 1, 4293 Dianalund, Denmark; University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.
Epilepsy Behav. 2023 Mar;140:109105. doi: 10.1016/j.yebeh.2023.109105. Epub 2023 Feb 7.
Encephalopathy related to Status Epilepticus during slow Sleep (ESES) is a childhood epilepsy syndrome characterized by the appearance of cognitive, behavioral, and motor disturbances in conjunction with a striking activation of EEG epileptic abnormalities during non-REM sleep. After more than 50 years since the first description, the pathophysiological mechanisms underlying the appearance of encephalopathy in association with a sleep-related enhancement of epileptic discharges are incompletely elucidated. Recent experimental data support the hypothesis that the development of the ESES encephalopathic picture depends on a spike-induced impairment of the synaptic homeostasis processes occurring during normal sleep and that is particularly pronounced during the developmental age. During sleep, synaptic homeostasis is promoted by synaptic weakening/elimination after the increment of synaptic strength that occurs during wakefulness. The EEG can display modifications in synaptic strength by changes in sleep slow wave activity (SWA). Recent studies during active ESES have failed to show changes in sleep SWA, while these changes occurred again after recovery from ESES, thus supporting a spike-related interference on the normal homeostatic processes of sleep. This impairment, during the developmental period, can lead to disruption of cortical wiring and brain plastic remodeling, which lead to the, often irreversible, neuropsychological compromise typical of ESES. From the nosographic point of view, these pathophysiological data lend support to the maintenance of the term ESES, i.e., "encephalopathy related to status epilepticus during sleep". Indeed, this term conveys the concept that the extreme activation of epileptic discharges during sleep is directly responsible for the encephalopathy, hence the importance of defining this condition as an encephalopathy related to the exaggerated activation of epileptic activity during sleep. In this respect, ESES represents a genuine example of a "pure" epileptic encephalopathy in which sleep-related epileptic activity "per se" has a crucial role in determining the encephalopathic picture. This paper was presented at the 8th London-Innsbruck Colloquium on Status Epilepticus and Acute Seizures held in September 2022.
慢波睡眠期癫痫性脑病(ESES)是一种儿童癫痫综合征,其特征为认知、行为和运动障碍,同时非快速眼动睡眠期脑电图癫痫异常显著激活。自首次描述以来已过去50多年,与睡眠相关的癫痫放电增强相关的脑病出现的病理生理机制仍未完全阐明。最近的实验数据支持这样一种假说,即ESES脑病表现的发展取决于正常睡眠期间发生的突触稳态过程因棘波诱导的损害,而这种损害在发育年龄阶段尤为明显。睡眠期间,清醒时突触强度增加后,突触通过减弱/消除来促进突触稳态。脑电图可通过睡眠慢波活动(SWA)的变化显示突触强度的改变。近期对活跃期ESES的研究未能显示睡眠SWA的变化,而从ESES恢复后这些变化再次出现,从而支持了棘波对正常睡眠稳态过程的干扰。在发育阶段,这种损害可导致皮质布线和脑可塑性重塑的破坏,进而导致ESES典型的、通常不可逆转的神经心理损害。从疾病分类学角度来看,这些病理生理数据支持保留“慢波睡眠期癫痫性脑病”这一术语,即“与睡眠期癫痫持续状态相关的脑病”。事实上,该术语传达了这样一个概念,即睡眠期间癫痫放电的极度激活直接导致了脑病,因此将这种情况定义为与睡眠期间癫痫活动过度激活相关的脑病非常重要。在这方面,ESES代表了一个真正的“纯”癫痫性脑病的例子,其中与睡眠相关的癫痫活动“本身”在确定脑病表现方面起着关键作用。本文在2022年9月举行的第8届伦敦 - 因斯布鲁克癫痫持续状态和急性癫痫研讨会上发表。