CNC.IBILI, Institute for Biomedical Imaging and Life Sciences, University of Coimbra, 3000-548, Coimbra, Portugal.
ICNAS, CIBIT, Institute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548, Coimbra, Portugal.
J Neurodev Disord. 2018 Mar 22;10(1):11. doi: 10.1186/s11689-018-9230-4.
Neurofibromatosis type1 (NF1) is associated with a broad range of behavioural deficits, and an imbalance between excitatory and inhibitory neurotransmission has been postulated in this disorder. Inhibition is involved in the control of frequency and stability of motor rhythms. Therefore, we aimed to explore the link between behavioural motor control, brain rhythms and brain activity, as assessed by EEG and fMRI in NF1.
We studied a cohort of 21 participants with NF1 and 20 age- and gender-matched healthy controls, with a finger-tapping task requiring pacing at distinct frequencies during EEG and fMRI scans.
We found that task performance was significantly different between NF1 and controls, the latter showing higher tapping time precision. The time-frequency patterns at the beta sub-band (20-26 Hz) mirrored the behavioural modulations, with similar cyclic synchronization/desynchronization patterns for both groups. fMRI results showed a higher recruitment of the extrapyramidal motor system (putamen, cerebellum and red nucleus) in the control group during the fastest pacing condition.
The present study demonstrated impaired precision in rhythmic pacing behaviour in NF1 as compared with controls. We found a decreased recruitment of the cerebellum, a structure where inhibitory interneurons are essential regulators of rhythmic synchronization, and in deep brain regions pivotally involved in motor pacing. Our findings shed light into the neural underpinnings of motor timing deficits in NF1.
神经纤维瘤病 1 型(NF1)与广泛的行为缺陷有关,并且在这种疾病中已经提出了兴奋性和抑制性神经递质之间的不平衡。抑制作用参与了运动节律的频率和稳定性的控制。因此,我们旨在通过 NF1 的 EEG 和 fMRI 评估来探索行为运动控制、脑节律和脑活动之间的联系。
我们研究了一组 21 名 NF1 患者和 20 名年龄和性别匹配的健康对照者,他们在 EEG 和 fMRI 扫描期间进行了要求以不同频率进行叩击的手指敲击任务。
我们发现 NF1 患者和对照组之间的任务表现有显著差异,后者显示出更高的叩击时间精度。β子带(20-26 Hz)的时频模式反映了行为调节,两组均显示出相似的循环同步/去同步模式。fMRI 结果显示,在最快的起搏条件下,对照组的锥体外系运动系统(壳核、小脑和红核)的募集更高。
本研究表明,与对照组相比,NF1 患者在节奏起搏行为方面存在精度受损。我们发现小脑的募集减少,小脑是抑制性中间神经元对节律同步至关重要的调节结构,并且在深部脑区域中,与运动起搏密切相关。我们的研究结果揭示了 NF1 中运动时间缺陷的神经基础。