首页> 外文期刊>Neuromodulation: journal of the International Neuromodulation Society >Resting Beta Hypersynchrony in Secondary Dystonia and Its Suppression During Pallidal Deep Brain Stimulation in DYT3+ Lubag Dystonia
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Resting Beta Hypersynchrony in Secondary Dystonia and Its Suppression During Pallidal Deep Brain Stimulation in DYT3+ Lubag Dystonia

机译:DYT3 + Lubag肌张力障碍的继发性肌张力障碍中的静息β超同步性及其在苍白的深脑刺激过程中的抑制。

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Objectives: 1) To characterize patterns of globus pallidus interna neural synchrony in patients with secondary dystonia; 2) to determine whether neural hypersynchrony in the globus pallidus externa (GPe) and interna (GPi) is attenuated during high frequency deep brain stimulation (HF DBS) in a patient with DYT3+ dystonia and in a patient with secondary dystonia due to childhood encephalitis.Materials and Methods: We recorded local field potentials from the DBS lead in the GPi of four patients (seven hemispheres) with secondary dystonia and from one patient (two hemispheres) with primary DYT3+ dystonia. In two patients, we also recorded pallidal local field potentials during the administration of 10 sec epochs of HF DBS.Results: Power spectral densities during rest demonstrated visible peaks in the beta band in seven out of nine cases. In DYT3+ dystonia, power in the alpha and beta bands, but not theta band, was attenuated during HF DBS in the GPe and in GPi, and attenuation was most prominent in the high beta band. This patient demonstrated an early and maintained improvement in dystonia. There was no beta peak and the power spectrum was not attenuated during HF DBS in a patient with secondary dystonia due to childhood encephalitis.Conclusions: These results suggest that beta hypersynchrony, demonstrated now in both primary and secondary dystonia, may play a pathophysiological role in pathological hyperkinesis. Further investigation is needed in a larger cohort of well-characterized primary and secondary dystonia patients.
机译:目的:1)表征继发性肌张力障碍患者苍白球的内部神经同步性; 2)确定在DYT3 +肌张力障碍患者和儿童期脑炎继发性肌张力障碍患者的高频深部脑刺激(HF DBS)期间,苍白球外部(GPe)和内在神经(GPi)的神经超合是否减弱。材料和方法:我们记录了4名继发性肌张力障碍患者和1名患者(两个半球)原发性DYT3 +肌张力障碍的GPi中DBS导联的局部场电位。在两名患者中,我们还在HF DBS的10 sep时期内记录了苍白的局部视野电位。结果:休息期间的功率谱密度显示9例中有7例的β谱带可见峰值。在DYT3 +肌张力障碍中,GPe和GPi中的HF DBS期间,α和β频段的功率衰减,但theta频段没有衰减,而高β频段的衰减最为明显。该患者表现出肌张力障碍的早期和持续改善。由于儿童期脑炎,继发性肌张力障碍患者在HF DBS期间没有β峰且功率谱未减弱。结论:这些结果表明,目前在原发性和继发性肌张力障碍中均表现出的β超共通性可能在肝硬化中发挥了病理生理作用。病理性运动亢进。在特征明确的原发性和继发性肌张力障碍患者的更大队列中,需要进一步的研究。

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