Association of Sleep Spindle Rate With Memory Consolidation in Children With Rolandic Epilepsy.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2025-01-28 Epub Date: 2024-12-30 DOI:10.1212/WNL.0000000000210232
Hunki Kwon, Dhinakaran M Chinappen, Elizabeth A Kinard, Skyler K Goodman, Jonathan F Huang, Erin D Berja, Katherine G Walsh, Wen Shi, Dara S Manoach, Mark A Kramer, Catherine J Chu
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Abstract

Background and objectives: Rolandic epilepsy (RE), the most common childhood focal epilepsy syndrome, is characterized by a transient period of sleep-activated epileptiform activity in the centrotemporal regions and variable cognitive deficits. Sleep spindles are prominent thalamocortical brain oscillations during sleep that have been mechanistically linked to sleep-dependent memory consolidation in animal models and healthy controls. Sleep spindles are decreased in RE and related sleep-activated epileptic encephalopathies. To further evaluate the association between this electrographic biomarker and cognitive dysfunction in this common disease, we investigate whether children with RE have deficient sleep-dependent memory consolidation and whether impaired memory consolidation is associated with reduced sleep spindles in the centrotemporal regions.

Methods: In this prospective case-control study, children were trained and tested on a validated probe of memory consolidation, the motor sequence task (MST). Sleep spindles were measured from high-density EEG during a 90-minute nap opportunity between MST training and testing using an automated sleep spindle detector validated for use in children with and without epilepsy.

Results: Twenty-three children with RE (9 with active disease, 5F, age 6.9-12.8 years; 14 with resolved disease, 8F, age 8.8-17.8 years) and 19 age-matched and sex-matched controls (8F, age 6.9-18.7 years) were enrolled. Children with active epilepsy had decreased memory consolidation compared with control children (p = 0.001, mean percentage reduction 25.7%, 95% CI 10.3%-41.2%) and compared with children with resolved epilepsy (p = 0.007, mean percentage reduction 21.9%, 95% CI 6.2%-37.6%). Children with active epilepsy had decreased sleep spindle rates in the centrotemporal region compared with controls (p = 0.008, mean decrease 2.5 spindles per minute, 95% CI 0.7-4.4 spindles per minute). Spindle rate, but not spike rate or spike-wave index, correlated with sleep-dependent memory consolidation (p = 0.004, mean MST improvement of 3.9%, 95% CI 1.3%-6.4%, for each unit increase in spindles per minute).

Discussion: Children with RE have impaired sleep-dependent memory consolidation during the active period of disease that correlates with a deficit in the sleep spindle rate. This finding identifies a noninvasive biomarker to aid diagnosis and a potential etiologic mechanism to guide therapeutic discovery of cognitive dysfunction in RE and related sleep-activated epilepsy syndromes.

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罗兰癫痫患儿睡眠纺锤体频率与记忆巩固的关系。
背景和目的:罗兰dic癫痫(RE)是最常见的儿童局灶性癫痫综合征,其特征是在中央颞叶区有一段短暂的睡眠激活的癫痫样活动和可变的认知缺陷。睡眠纺锤波是睡眠期间显著的丘脑皮质脑振荡,在动物模型和健康对照中与睡眠依赖性记忆巩固有机制联系。睡眠纺锤波在RE和相关睡眠激活性癫痫性脑病中减少。为了进一步评估这种电图生物标志物与这种常见疾病的认知功能障碍之间的关系,我们研究了RE患儿是否存在睡眠依赖性记忆巩固缺陷,以及记忆巩固受损是否与中央颞叶区域睡眠纺锤波减少有关。方法:在这项前瞻性病例对照研究中,儿童接受了一种有效的记忆巩固探针——运动序列任务(MST)的训练和测试。睡眠纺锤波是在MST训练和测试之间90分钟的午睡时间内通过高密度脑电图测量的,使用的是一种自动睡眠纺锤波检测器,该检测器已被证实可用于有癫痫和无癫痫的儿童。结果:RE患儿23例(伴活动性疾病9例,5岁,年龄6.9 ~ 12.8岁;纳入14例疾病解决的患者(8F,年龄8.8-17.8岁)和19例年龄匹配和性别匹配的对照组(8F,年龄6.9-18.7岁)。与对照组相比,活动性癫痫患儿的记忆巩固减少(p = 0.001,平均减少25.7%,95% CI 10.3%-41.2%),与消退性癫痫患儿相比(p = 0.007,平均减少21.9%,95% CI 6.2%-37.6%)。与对照组相比,活动性癫痫患儿的中央颞叶区睡眠纺锤波率降低(p = 0.008,平均降低2.5纺锤波/分钟,95% CI 0.7-4.4纺锤波/分钟)。纺锤波速率与睡眠依赖性记忆巩固相关,但与尖波速率或尖波指数无关(p = 0.004,每分钟每增加一个单位的纺锤波,平均MST改善3.9%,95% CI为1.3%-6.4%)。讨论:患有RE的儿童在疾病活动期睡眠依赖性记忆巩固受损,这与睡眠纺锤体速率的缺陷有关。这一发现确定了一种非侵入性的生物标志物来帮助诊断和潜在的病因学机制,以指导RE和相关睡眠激活性癫痫综合征的认知功能障碍的治疗发现。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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