自闭症青少年运动模仿时的神经磁性 Beta 波段振荡。

Autism Research and Treatment Pub Date : 2018-07-25 eCollection Date: 2018-01-01 DOI:10.1155/2018/9035793
I Buard, E Kronberg, S Steinmetz, S Hepburn, D C Rojas
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摘要

患有 ASD 的儿童可能由于低水平的感官或运动障碍,往往在早期表现出动作模仿困难。有研究表明,患有 ASD 的成年人在动作模仿过程中大脑皮层节律受损。虽然这些振荡反映了一个与年龄相关的过程,但在患有 ASD 的青少年身上还没有得到充分的研究。我们收集了脑磁图数据,研究了 14 名患有自闭症的青少年和 14 名未患有自闭症的青少年在完成精细动作模仿任务时,在μ(8-13 赫兹)和β频率(15-30 赫兹)范围内的振荡活动模式。发育正常的青少年表现出与成人相似的运动信号模式,如在运动前和运动过程中与事件相关的贝塔和μ失同步(ERD),以及运动后的贝塔反弹(PMBR)。相比之下,患有 ASD 的患者表现出更强的β和μ-ERD以及更弱的 PMBR。尽管运动皮层振荡存在差异,但各组之间的行为表现相似。最后,我们观察到,在发育正常的儿童中,PBMR和β-ERD的增加与年龄有关,但在自闭症组中却不存在这种相关性。这些结果表明,在完整的运动模仿过程中,自闭症青少年大脑皮层节律的抑制驱动力减弱。此外,自闭症患者大脑运动信号的障碍可能并非由于大脑发育迟缓所致。从自闭症兴奋-抑制失衡的角度来看,我们对神经生理网络组织的改变提出了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Neuromagnetic Beta-Band Oscillations during Motor Imitation in Youth with Autism.

Children with ASD often exhibit early difficulties with action imitation, possibly due to low-level sensory or motor impairments. Impaired cortical rhythms have been demonstrated in adults with ASD during motor imitation. While those oscillations reflect an age-dependent process, they have not been fully investigated in youth with ASD. We collected magnetoencephalography data to examine patterns of oscillatory activity in the mu (8-13 Hz) and beta frequency (15-30 Hz) range in 14 adolescents with and 14 adolescents without ASD during a fine motor imitation task. Typically developing adolescents exhibited adult-like patterns of motor signals, e.g., event-related beta and mu desynchronization (ERD) before and during the movement and a postmovement beta rebound (PMBR) after the movement. In contrast, those with ASD exhibited stronger beta and mu-ERD and reduced PMBR. Behavioral performance was similar between groups despite differences in motor cortical oscillations. Finally, we observed age-related increases in PBMR and beta-ERD in the typically developing children, but this correlation was not present in the autism group. These results suggest reduced inhibitory drive in cortical rhythms in youth with autism during intact motor imitation. Furthermore, impairments in motor brain signals in autism may not be due to delayed brain development. In the context of the excitation-inhibition imbalance perspectives of autism, we offer new insights into altered organization of neurophysiological networks.

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