The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders

被引:251
作者
Spence, Sarah J. [1 ]
Schneider, Mark T. [1 ]
机构
[1] NIMH, Pediat & Dev Neurosci Branch, NIH, Bethesda, MD 20892 USA
关键词
PERVASIVE DEVELOPMENTAL DISORDER; RETT-SYNDROME; COGNITIVE IMPAIRMENT; TUBEROUS SCLEROSIS; LANGUAGE REGRESSION; ROLANDIC EPILEPSY; SEIZURE DISORDERS; CONVULSIVE DISORDER; MENTAL-RETARDATION; CLINICAL SEIZURES;
D O I
10.1203/PDR.0b013e31819e7168
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Autism is a neurodevelopmental disorder of unknown etiology characterized by social and communication deficits and the presence of restricted interests/repetitive behaviors. Higher rates of epilepsy have long been reported, but prevalence estimates vary from as little its 5% to as much as 46%. This variation is probably the result of sample characteristics that increase epilepsy risk such as sample ascertainment, lower intelligence quotient (IQ), the inclusion of patients with nonidiopathic autism, age, and gender. However, critical review of the literature reveals that the rate in idiopathic cases with normal IQ is still significantly above the population risk suggesting that autism itself is associated with an increased risk of epilepsy. Recently, there has been interest in the Occurrence of epileptiform electroencephalograms (EEGs) even in the absence of epilepsy. Rates as high as 60% have been reported and some investigators propose that these abnormalities may play a Causal role in the autism phenotype. Although this phenomenon is still not well understood and risk factors have yet to be determined, the treatment implications are increasingly important, We review the recent literature to elucidate possible risk factors for both epilepsy and epileptiform EEGs. We then review existing data and discuss controversies surrounding treatment of EEG abnormalities. (Pediatr Res 65: 599-606, 2009)
引用
收藏
页码:599 / 606
页数:8
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