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闭环深部脑刺激治疗帕金森病中药物难治性步态冻结

Closed-Loop Deep Brain Stimulation to Treat Medication-Refractory Freezing of Gait in Parkinson's Disease.

作者信息

Molina Rene, Hass Chris J, Cernera Stephanie, Sowalsky Kristen, Schmitt Abigail C, Roper Jaimie A, Martinez-Ramirez Daniel, Opri Enrico, Hess Christopher W, Eisinger Robert S, Foote Kelly D, Gunduz Aysegul, Okun Michael S

机构信息

Department of Electrical and Computer Engineering, University of Florida, Gainesville, FL, United States.

Norman Fixel Institute for Neurological Diseases and The Program for Movement Disorders and Neurorestoration, University of Florida, Gainesville, FL, United States.

出版信息

Front Hum Neurosci. 2021 Mar 1;15:633655. doi: 10.3389/fnhum.2021.633655. eCollection 2021.

Abstract

: Treating medication-refractory freezing of gait (FoG) in Parkinson's disease (PD) remains challenging despite several trials reporting improvements in motor symptoms using subthalamic nucleus or globus pallidus internus (GPi) deep brain stimulation (DBS). Pedunculopontine nucleus (PPN) region DBS has been used for medication-refractory FoG, with mixed findings. FoG, as a paroxysmal phenomenon, provides an ideal framework for the possibility of closed-loop DBS (CL-DBS). : In this clinical trial (NCT02318927), five subjects with medication-refractory FoG underwent bilateral GPi DBS implantation to address levodopa-responsive PD symptoms with open-loop stimulation. Additionally, PPN DBS leads were implanted for CL-DBS to treat FoG. The primary outcome of the study was a 40% improvement in medication-refractory FoG in 60% of subjects at 6 months when "on" PPN CL-DBS. Secondary outcomes included device feasibility to gauge the recruitment potential of this four-lead DBS approach for a potentially larger clinical trial. Safety was judged based on adverse events and explantation rate. : The feasibility of this approach was demonstrated as we recruited five subjects with both "on" and "off" medication freezing. The safety for this population of patients receiving four DBS leads was suboptimal and associated with a high explantation rate of 40%. The primary clinical outcome in three of the five subjects was achieved at 6 months. However, the group analysis of the primary clinical outcome did not reveal any benefit. : This study of a human PPN CL-DBS trial in medication-refractory FoG showed feasibility in recruitment, suboptimal safety, and a heterogeneous clinical effect in FoG outcomes.

摘要

尽管有多项试验报告称,使用丘脑底核或苍白球内侧部(GPi)深部脑刺激(DBS)可改善帕金森病(PD)的运动症状,但治疗药物难治性步态冻结(FoG)仍然具有挑战性。脚桥核(PPN)区域DBS已用于治疗药物难治性FoG,结果不一。FoG作为一种阵发性现象,为闭环DBS(CL-DBS)的可能性提供了理想的框架。

在这项临床试验(NCT02318927)中,五名患有药物难治性FoG的受试者接受了双侧GPi DBS植入,以通过开环刺激解决左旋多巴反应性PD症状。此外,植入了PPN DBS电极用于CL-DBS以治疗FoG。该研究的主要结果是,在6个月时,60%的受试者在开启PPN CL-DBS时,药物难治性FoG改善40%。次要结果包括设备可行性,以评估这种四电极DBS方法在潜在更大规模临床试验中的招募潜力。根据不良事件和取出率判断安全性。

我们招募了五名在服药和未服药时均有冻结现象的受试者,证明了这种方法的可行性。接受四根DBS电极的这组患者的安全性不理想,取出率高达40%。五名受试者中有三名在6个月时达到了主要临床结果。然而,主要临床结果的组间分析未显示任何益处。

这项针对药物难治性FoG的人体PPN CL-DBS试验研究表明,在招募方面具有可行性,安全性不理想,且FoG结果的临床效果存在异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4178/7959768/6d0634d911e7/fnhum-15-633655-g0001.jpg

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