Institute of Mental Health, Belgrade, Serbia; Faculty of Special Education and Rehabilitation, University of Belgrade, Belgrade, Serbia.
Institute of Mental Health, Belgrade, Serbia.
Epilepsy Behav. 2019 Mar;92:45-52. doi: 10.1016/j.yebeh.2018.12.011. Epub 2019 Jan 3.
The purpose of this study was to determine the prevalence of epilepsy and subclinical epileptiform abnormalities in children with autism spectrum disorder (ASD), and to investigate its effects on core autistic symptoms and adaptive behavior skills.
Patients with diagnosis of ASD who met full criteria on Autism Diagnostic Interview-Revised (ADI-R) were included in the study. Adaptive behavior skills were assessed by Vineland Adaptive Behavior Scale-II (VABS-II). Clinical assessment for epilepsy and video electroencephalography (EEG) (v-EEG) examinations during wakefulness and/or sleep were prospectively performed in all patients.
A total of 112 patients with diagnosis of ASD of mean age 6.58 ± 3.72 were included in the study. Based on clinical and v-EEG assessments, three groups of patients were defined: 1) patients with epilepsy (n = 17; 15.2%); 2) patients with epileptiform discharges in absence of clinical seizures (n = 14; 12.5%); 3) patients without epilepsy and without epileptiform discharges (n = 81; 72.3%). There were no significant differences between three groups of patients on ADI-R subscores. Speech development was also not significantly related to epilepsy. There was a slight tendency of the VABS-II motor skills score to be higher in the group of patients with autism without clinical diagnosis of epilepsy and without subclinical epileptiform discharges (p < 0.05) in comparison with the two other groups. According to this tendency, we might claim that patients with higher scores on motor skills could have 0.88 times lower odds for having epileptiform EEG activity.
According to our results, we were not able to detect differences in the ADI-R between the three populations with ASD, all with unknown etiology. Epilepsy, as well as subclinical epileptic discharges, showed small effects on Motor Skills in patients with autism, and had no effect on adaptive behavior Communication/Socialization/Daily Living Skills.
本研究旨在确定自闭症谱系障碍(ASD)儿童中癫痫和亚临床癫痫样异常的患病率,并探讨其对核心自闭症症状和适应行为技能的影响。
符合自闭症诊断访谈修订版(ADI-R)完全标准的 ASD 患者纳入本研究。适应行为技能采用 Vineland 适应行为量表-II(VABS-II)进行评估。所有患者均前瞻性进行临床癫痫评估和视频脑电图(EEG)(v-EEG)检查,包括清醒和/或睡眠期间。
共有 112 名符合 ASD 诊断的患者,平均年龄为 6.58±3.72 岁。根据临床和 v-EEG 评估,将患者分为三组:1)癫痫组(n=17;15.2%);2)无临床发作的癫痫样放电组(n=14;12.5%);3)无癫痫和无癫痫样放电组(n=81;72.3%)。三组患者在 ADI-R 子量表上无显著差异。言语发育也与癫痫无显著相关性。在无临床诊断癫痫和无亚临床癫痫样放电的自闭症患者中,VABS-II 运动技能评分略高(p<0.05),与其他两组相比。根据这一趋势,我们可以声称运动技能得分较高的患者发生癫痫样 EEG 活动的可能性降低 0.88 倍。
根据我们的结果,我们无法在三组 ASD 患者中(均病因不明)检测到 ADI-R 之间的差异。癫痫以及亚临床癫痫样放电对自闭症患者的运动技能有较小的影响,对沟通/社交/日常生活技能的适应行为没有影响。