Evidence map›Paper›PMID 37693765›Full record

ArticleFrontiers in neurology2023

Myogenic and cortical evoked potentials vary as a function of stimulus pulse geometry delivered in the subthalamic nucleus of Parkinson's disease patients.

Brett A Campbell, Leonardo Favi Bocca, Jakov Tiefenbach, Olivia Hogue, Sean J Nagel, Richard Rammo, David Escobar Sanabria, Andre G Machado, Kenneth B Baker

Abstract read
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Article in Frontiers in neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Brett A CampbellDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United States.
Leonardo Favi BoccaCenter for Neurological Restoration, Cleveland Clinic, Cleveland, OH, United States.
Jakov TiefenbachDepartment of Neurosciences, Cleveland Clinic, Cleveland, OH, United States.
Olivia HogueCenter for Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, United States.
Sean J NagelCenter for Neurological Restoration, Cleveland Clinic, Cleveland, OH, United States.
Richard RammoCenter for Neurological Restoration, Cleveland Clinic, Cleveland, OH, United States.
David Escobar SanabriaCenter for Neurological Restoration, Cleveland Clinic, Cleveland, OH, United States.
Andre G MachadoDepartment of Neurosciences, Cleveland Clinic, Cleveland, OH, United States.
Kenneth B BakerDepartment of Neurosciences, Cleveland Clinic, Cleveland, OH, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The therapeutic efficacy of deep brain stimulation (DBS) of the subthalamic nucleus (STN) for Parkinson's disease (PD) may be limited for some patients by the presence of stimulation-related side effects. Such effects are most often attributed to electrical current spread beyond the target region. Prior computational modeling studies have suggested that changing the degree of asymmetry of the individual phases of the biphasic, stimulus pulse may allow for more selective activation of neural elements in the target region. To the extent that different neural elements contribute to the therapeutic vs. side-effect inducing effects of DBS, such improved selectivity may provide a new parameter for optimizing DBS to increase the therapeutic window. Methods: We investigated the effect of six different pulse geometries on cortical and myogenic evoked potentials in eight patients with PD whose leads were temporarily externalized following STN DBS implant surgery. DBS-cortical evoked potentials were quantified using peak to peak measurements and wavelets and myogenic potentials were quantified using RMS. Results: We found that the slope of the recruitment curves differed significantly as a function of pulse geometry for both the cortical- and myogenic responses. Notably, this effect was observed most frequently when stimulation was delivered using a monopolar, as opposed to a bipolar, configuration. Discussion: Manipulating pulse geometry results in differential physiological effects at both the cortical and neuromuscular level. Exploiting these differences may help to expand DBS' therapeutic window and support the potential for incorporating pulse geometry as an additional parameter for optimizing therapeutic benefit.

Indexed as

cortical evoked potentialsdeep brain stimulationmotor evoked potentialParkinson’s diseasepulse geometrysubthalamic nucleus

Identifiers

PMID37693765
PMCPMC10484227

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.