Chan Samantha, Pressler Ronit, Boyd Stewart G, Baldeweg Torsten, Cross J Helen
Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Great Ormond Street Hospital NHS Trust, London, United Kingdom.
Epilepsia. 2017 Mar;58(3):456-466. doi: 10.1111/epi.13668. Epub 2017 Jan 23.
Children with epilepsy have high rates of both cognitive impairment and sleep disruption. It is thus assumed that sleep-dependent memory consolidation is vulnerable to ongoing epileptic activity, but direct evidence of this is limited.
We performed a within-subject comparison of memory retention across intervals of wake or overnight sleep. Healthy children (n = 21, 6-16 years, 12 female) and children with focal epilepsy (n = 22, 6-16 years, 9 female) performed verbal and visuospatial memory tasks under each condition. Sleep was assessed with electroencephalography (EEG) polysomnography during the overnight interval. Interictal discharges were quantified manually.
Memory retention was greater in the sleep condition in both the verbal (F = 10.8, p = 0.002, Cohen's d = 0.67) and the visuospatial (F = 4.23, p = 0.05, Cohen's d = 0.40) tasks, with no significant interaction of group by condition in either task. Across the total sample, gain in memory retention with sleep in the verbal task correlated with duration of slow wave sleep (r = 0.4, p = 0.01). In patients, sleep-dependent memory consolidation was negatively correlated with interictal discharge rate in both the verbal (ρ = -0.49, p = 0.04) and visuospatial (ρ = -0.45, p = 0.08) tasks. On post hoc analysis, a longer history of epilepsy (r = 0.53, p = 0.01) and a temporal (t = 1.8, p = 0.1, Cohen's d = 0.86) rather than an extratemporal seizure focus (t = 0.8, p = 0.4, Cohen's d = 0.30) was associated with greater contribution of sleep to verbal memory retention.
We have demonstrated that memory consolidation in children with focal epilepsy benefits from sleep, showing the same correlation with slow wave sleep as in healthy children, but an inverse relationship with the interictal discharge load during sleep. This mechanism appears to be increasingly recruited with longer duration of illness, indicating a resilient homeostatic function which may be harnessed to aid learning.
癫痫患儿认知障碍和睡眠中断的发生率都很高。因此推测,依赖睡眠的记忆巩固易受持续癫痫活动的影响,但这方面的直接证据有限。
我们在清醒或夜间睡眠间隔内对记忆保持进行了受试者内比较。健康儿童(n = 21,6 - 16岁,12名女性)和局灶性癫痫患儿(n = 22,6 - 16岁,9名女性)在每种条件下进行言语和视觉空间记忆任务。夜间睡眠期间通过脑电图(EEG)多导睡眠图评估睡眠情况。发作间期放电通过人工进行量化。
在言语任务(F = 10.8,p = 0.002,Cohen's d = 0.67)和视觉空间任务(F = 4.23,p = 0.05,Cohen's d = 0.40)中,睡眠条件下的记忆保持都更好,且在这两个任务中,组与条件之间均无显著交互作用。在整个样本中,言语任务中睡眠导致的记忆保持增益与慢波睡眠持续时间相关(r = 0.4,p = 0.01)。在患者中,依赖睡眠的记忆巩固在言语任务(ρ = -0.49,p = 0.04)和视觉空间任务(ρ = -0.45,p = 0.08)中均与发作间期放电率呈负相关。事后分析显示,癫痫病史较长(r = 0.53,p = 0.01)以及颞叶(t = 1.8,p = 0.1,Cohen's d = 0.86)而非颞叶外癫痫病灶(t = 0.8,p = 0.4,Cohen's d = 0.30)与睡眠对言语记忆保持的更大贡献相关。
我们已经证明,局灶性癫痫患儿的记忆巩固受益于睡眠,与健康儿童一样与慢波睡眠存在相同的相关性,但与睡眠期间的发作间期放电负荷呈负相关。随着病程延长,这种机制似乎越来越多地被调用,表明存在一种可用于辅助学习的弹性稳态功能。