scholarly journals Factors correlated with therapeutic effects of globus pallidus deep brain stimulation on freezing of gait in advanced Parkinson's disease: A pilot study

Author(s):  
Seung Hyun Lee ◽  
Jooyoung Lee ◽  
Mi Sun Kim ◽  
Yun Su Hwang ◽  
Sungyang Jo ◽  
...  
Author(s):  
Stephano Chang ◽  
Iahn Cajigas ◽  
James D. Guest ◽  
Brian R. Noga ◽  
Corneliu C. Luca ◽  
...  

Abstract Background: Freezing of gait (FOG) is a particularly debilitating motor deficit seen in a subset of Parkinson’s Disease (PD) patients that is poorly responsive to standard levodopa therapy or deep brain stimulation (DBS) of established PD targets such as the subthalamic nucleus and the globus pallidus interna. The proposal of a DBS target in the midbrain, known as the pedunculopontine nucleus (PPN) to address FOG was based on its observed pathology in PD and its hypothesized involvement in locomotor control as a part of the mesencephalic locomotor region, a functionally defined area of the midbrain that elicits locomotion in both intact animals and decerebrate animal preparations with electrical stimulation. Initial reports of PPN DBS were met with much enthusiasm; however, subsequent studies produced mixed results, and recent meta-analysis results have been far less convincing than initially expected. A closer review of the extensive MLR preclinical literature, including recent optogenetics studies, strongly suggests that the closely related cuneiform nucleus (CnF), just dorsal to the PPN, may be a superior target to promote gait initiation.Methods: We will conduct a prospective, open-label, single-arm pilot study to assess safety and feasibility of CnF DBS in PD patients with levodopa-refractory FOG. Four patients will receive CnF DBS and have gait assessments with and without DBS during a 6-month follow up.Discussion: This paper presents the study design and rationale for a pilot study investigating a novel DBS target for gait dysfunction, including targeting considerations. This pilot study is intended to support future larger scale clinical trials investigating this target.Trial Registration: Clinicaltrials.gov Identifier: NCT04218526 (registered January 6, 2020), https://www.clinicaltrials.gov/ct2/show/NCT04218526


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Stephano J. Chang ◽  
Iahn Cajigas ◽  
James D. Guest ◽  
Brian R. Noga ◽  
Eva Widerström-Noga ◽  
...  

Abstract Background Freezing of gait (FOG) is a particularly debilitating motor deficit seen in a subset of Parkinson’s disease (PD) patients that is poorly responsive to standard levodopa therapy or deep brain stimulation (DBS) of established PD targets such as the subthalamic nucleus and the globus pallidus interna. The proposal of a DBS target in the midbrain, known as the pedunculopontine nucleus (PPN) to address FOG, was based on its observed pathology in PD and its hypothesized involvement in locomotor control as a part of the mesencephalic locomotor region, a functionally defined area of the midbrain that elicits locomotion in both intact animals and decerebrate animal preparations with electrical stimulation. Initial reports of PPN DBS were met with much enthusiasm; however, subsequent studies produced mixed results, and recent meta-analysis results have been far less convincing than initially expected. A closer review of the extensive mesencephalic locomotor region (MLR) preclinical literature, including recent optogenetics studies, strongly suggests that the closely related cuneiform nucleus (CnF), just dorsal to the PPN, may be a superior target to promote gait initiation. Methods We will conduct a prospective, open-label, single-arm pilot study to assess safety and feasibility of CnF DBS in PD patients with levodopa-refractory FOG. Four patients will receive CnF DBS and have gait assessments with and without DBS during a 6-month follow-up. Discussion This paper presents the study design and rationale for a pilot study investigating a novel DBS target for gait dysfunction, including targeting considerations. This pilot study is intended to support future larger scale clinical trials investigating this target. Trial registration ClinicalTrials.gov identifier: NCT04218526 (registered January 6, 2020)


2021 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Xia Shi ◽  
Ziheng Zhang

<p style='text-indent:20px;'>Deep brain stimulation (DBS) alleviates the symptoms of tremor, rigidity, and akinesia of the Parkinson's disease (PD). Over decades of the clinical experience, subthalamic nucleus (STN), globus pallidus externa (GPe) and globus pallidus internal (GPi) have been chosen as the common DBS target sites. However, how to design the DBS waveform is still a challenging problem. There is evidence that chronic high-frequency stimulation may cause long-term tissue damage and other side effects. In this paper, we apply a form of DBS with delayed rectangular waveform, denoted as pulse-delay-pulse (PDP) type DBS, on multiple-site based on a computational model of the basal ganglia-thalamus (BG-TH) network. We mainly investigate the effects of the stimulation frequency on relay reliability of the thalamus neurons, beta band oscillation of GPi nucleus and firing rate of the BG network. The results show that the PDP-type DBS at STN-GPe site results in better performance at lower frequencies, while the DBS at GPi-GPe site causes the number of spikes of STN to decline and deviate from the healthy status. Fairly good therapeutic effects can be achieved by PDP-type DBS at STN-GPi site only at higher frequencies. Thus, it is concluded that the application of multiple-site stimulation with PDP-type DBS at STN-GPe is of great significance in treating symptoms of neurological disorders in PD.</p>


2015 ◽  
Vol 12 (6) ◽  
pp. 066013 ◽  
Author(s):  
Gerrit E Gmel ◽  
Tara J Hamilton ◽  
Milan Obradovic ◽  
Robert B Gorman ◽  
Peter S Single ◽  
...  

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