Department of Neurology, Berenson-Allen Center for Noninvasive Brain Stimulation, Beth Israel Deaconess Medical Center - Harvard Medical School Boston, MA, USA ; Neuromodulation Program and Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital - Harvard Medical School Boston, MA, USA ; Neuroplasticity and Autism Spectrum Disorder Program, E. P. Bradley Hospital, East Providence, RI USA ; Department of Psychiatry and Human Behavior, Warren Alpert Medical School of Brown University, East Providence, RI USA.
Department of Neurology, Berenson-Allen Center for Noninvasive Brain Stimulation, Beth Israel Deaconess Medical Center - Harvard Medical School Boston, MA, USA.
Front Hum Neurosci. 2014 Aug 13;8:627. doi: 10.3389/fnhum.2014.00627. eCollection 2014.
The developmental pathophysiology of autism spectrum disorders (ASD) is currently not fully understood. However, multiple lines of evidence suggest that the behavioral phenotype may result from dysfunctional inhibitory control over excitatory synaptic plasticity. Consistent with this claim, previous studies indicate that adults with Asperger's Syndrome show an abnormally extended modulation of corticospinal excitability following a train of repetitive transcranial magnetic stimulation (rTMS). As ASD is a developmental disorder, the current study aimed to explore the effect of development on the duration of modulation of corticospinal excitability in children and adolescents with ASD. Additionally, as the application of rTMS to the understanding and treatment of pediatric neurological and psychiatric disorders is an emerging field, this study further sought to provide evidence for the safety and tolerability of rTMS in children and adolescents with ASD. Corticospinal excitability was measured by applying single pulses of TMS to the primary motor cortex both before and following a 40 s train of continuous theta burst stimulation. 19 high-functioning males ages 9-18 with ASD participated in this study. Results from this study reveal a positive linear relationship between age and duration of modulation of rTMS after-effects. Specifically we found that the older participants had a longer lasting response. Furthermore, though the specific protocol employed typically suppresses corticospinal excitability in adults, more than one third of our sample had a paradoxical facilitatory response to the stimulation. Results support the safety and tolerability of rTMS in pediatric clinical populations. Data also support published theories implicating aberrant plasticity and GABAergic dysfunction in this population.
自闭症谱系障碍(ASD)的发育发病机制目前尚未完全了解。然而,有多种证据表明,行为表型可能是由于兴奋性突触可塑性的抑制控制功能障碍所致。与这一说法一致的是,先前的研究表明,阿斯伯格综合征患者在接受重复经颅磁刺激(rTMS)的一连串刺激后,皮质脊髓兴奋性的调制时间会出现异常延长。由于 ASD 是一种发育障碍,因此本研究旨在探讨发育对 ASD 儿童和青少年皮质脊髓兴奋性调制持续时间的影响。此外,由于 rTMS 在理解和治疗儿科神经和精神疾病方面的应用是一个新兴领域,因此本研究还旨在为 ASD 儿童和青少年 rTMS 的安全性和耐受性提供证据。通过在初级运动皮层施加单个 TMS 脉冲,在连续 theta 爆发刺激 40 秒的刺激前后测量皮质脊髓兴奋性。19 名年龄在 9 至 18 岁之间的高功能男性 ASD 患者参与了这项研究。本研究的结果显示,rTMS 后效应调制的持续时间与年龄之间存在正线性关系。具体来说,我们发现年龄较大的参与者的反应持续时间更长。此外,尽管采用的特定方案通常会抑制成人的皮质脊髓兴奋性,但我们的样本中有超过三分之一的人对刺激有反常的促进反应。结果支持 rTMS 在儿科临床人群中的安全性和耐受性。数据还支持发表的理论,即该人群中存在异常可塑性和 GABA 能功能障碍。