Hitting the brakes: pathological subthalamic nucleus activity in Parkinson's disease gait freezing.

M. Georgiades, J. Shine, M. Gilat, J. McMaster, B. Owler, N. Mahant, S. Lewis
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引用次数: 30

Abstract

Gait freezing is a complex and devastating paroxysmal motor arrest commonly suffered in Parkinson's disease that causes significant impairment to mobility, commonly resulting in falls and subsequent injury. The neurobiological basis of gait freezing in Parkinson's disease is poorly understood and thus, currently available therapies are partially effective at best. We used a validated virtual reality gait paradigm to elicit freezing behaviour intraoperatively in eight patients undergoing subthalamic nucleus deep brain stimulation surgery while microelectrode recordings were obtained. This allowed us to directly test the hypothesis that increases in pathological multi-unit activity in the subthalamic nucleus are associated with freezing onset in real time, manifest as dysfunctional firing of lower limb muscles typical of freezing that were detected by EMG. We present evidence that freezing is related to transient increases in pathological subthalamic nucleus activity. We performed time-frequency analysis to characterize the oscillatory dynamics of subthalamic nucleus activity coincident with freezing onset, demonstrating an increase in pathological beta and theta rhythms that are followed by a temporal chain of activity culminating in characteristically abnormal lower limb muscle firing detected by EMG. Finally, we interrogate the potential clinical utility of our findings by contrasting the subthalamic nucleus activity signature during pathological freezing against purposeful stopping. These results advance our understanding of the neurobiological basis of gait freezing in Parkinson's disease, highlighting the role of the subthalamic nucleus and emergent synchronous activity in basal ganglia circuits in driving non-purposeful motor arrests in individuals with Parkinson's disease. Pathological subthalamic nucleus activity identified in association with freezing is discernible from that of volitional stopping, paving the way towards more effective therapeutics such as adaptive closed-loop deep brain stimulation protocols.
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踩刹车:帕金森病步态冻结的病理性丘脑下核活动。
步态冻结是一种复杂的、毁灭性的阵发性运动停止,常见于帕金森氏症,导致活动能力严重受损,通常导致跌倒和随后的损伤。帕金森病中步态冻结的神经生物学基础尚不清楚,因此,目前可用的治疗方法充其量是部分有效的。我们使用一种经过验证的虚拟现实步态模式来诱导8名接受丘脑下核深部脑刺激手术的患者术中冻结行为,同时获得微电极记录。这使我们能够直接验证这样的假设,即丘脑下核病理性多单位活动的增加与实时冻结发作有关,表现为肌电图检测到的典型冻结下肢肌肉的功能障碍放电。我们提出的证据表明,冷冻与病理性丘脑下核活动的短暂增加有关。我们进行了时频分析,以表征与冻结发作同时发生的丘脑底核活动的振荡动力学,结果显示病理性β和θ节律的增加,随后是肌电图检测到的具有特征性异常下肢肌肉放电的时间链活动。最后,我们通过对比病理冻结和有目的停止期间的丘脑下核活动特征,来询问我们的发现的潜在临床应用。这些结果促进了我们对帕金森病患者步态冻结的神经生物学基础的理解,强调了丘脑下核和基底神经节回路中出现的同步活动在驱动帕金森病患者非目的运动骤停中的作用。与冷冻相关的病理性丘脑底核活动与自愿停止相关,这为更有效的治疗方法(如适应性闭环脑深部刺激方案)铺平了道路。
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