Movement Disorders (revue)

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Effects of Deep Brain Stimulation and Medication on Strength, Bradykinesia, and Electromyographic Patterns of the Ankle Joint in Parkinson’s Disease

Identifieur interne : 001417 ( Ncbi/Merge ); précédent : 001416; suivant : 001418

Effects of Deep Brain Stimulation and Medication on Strength, Bradykinesia, and Electromyographic Patterns of the Ankle Joint in Parkinson’s Disease

Auteurs : David E. Vaillancourt [États-Unis] ; Janey Prodoehl [États-Unis] ; Molly M. Sturman [États-Unis] ; Roy A. E. Bakay [États-Unis] ; Leo Verhagen Metman [États-Unis] ; Daniel M. Corcos [États-Unis]

Source :

RBID : PMC:2373255

English descriptors

Abstract

We investigated the control of movement in 12 patients with Parkinson’s disease (PD) after they received surgically implanted high-frequency stimulating electrodes in the subthalamic nucleus (STN). The experiment studied ankle strength, movement velocity, and the associated electromyographic patterns in PD patients, six of whom had tremor at the ankle. The patients were studied off treatment, ON STN deep brain stimulation (DBS), on medication, and on medication plus STN DBS. Twelve matched control subjects were also examined. Medication alone and STN DBS alone increased patients’ ankle strength, ankle velocity, agonist muscle burst amplitude, and agonist burst duration, while reducing the number of agonist bursts during movement. These findings were similar for PD patients with and without tremor. The combination of medication plus STN DBS normalized maximal strength at the ankle joint, but ankle movement velocity and electromyographic patterns were not normalized. The findings are the first to demonstrate that STN DBS and medication increase strength and movement velocity at the ankle joint.


Url:
DOI: 10.1002/mds.20672
PubMed: 16124011
PubMed Central: 2373255

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PMC:2373255

Le document en format XML

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<term>Ankle Joint (innervation)</term>
<term>Antiparkinson Agents (administration & dosage)</term>
<term>Antiparkinson Agents (adverse effects)</term>
<term>Biomechanical Phenomena</term>
<term>Carbidopa (administration & dosage)</term>
<term>Carbidopa (adverse effects)</term>
<term>Combined Modality Therapy</term>
<term>Deep Brain Stimulation (methods)</term>
<term>Electrodes, Implanted</term>
<term>Electromyography (drug effects)</term>
<term>Humans</term>
<term>Hypokinesia (physiopathology)</term>
<term>Hypokinesia (therapy)</term>
<term>Isometric Contraction (drug effects)</term>
<term>Isometric Contraction (physiology)</term>
<term>Levodopa (administration & dosage)</term>
<term>Levodopa (adverse effects)</term>
<term>Muscle Weakness (physiopathology)</term>
<term>Muscle Weakness (therapy)</term>
<term>Muscle, Skeletal (innervation)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (physiopathology)</term>
<term>Parkinson Disease (therapy)</term>
<term>Reference Values</term>
<term>Signal Processing, Computer-Assisted</term>
<term>Statistics as Topic</term>
<term>Torque</term>
<term>Treatment Outcome</term>
<term>Tremor (physiopathology)</term>
<term>Tremor (therapy)</term>
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<term>Carbidopa</term>
<term>Levodopa</term>
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<term>Antiparkinson Agents</term>
<term>Carbidopa</term>
<term>Levodopa</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Electromyography</term>
<term>Isometric Contraction</term>
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<term>Muscle, Skeletal</term>
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<term>Muscle Weakness</term>
<term>Parkinson Disease</term>
<term>Tremor</term>
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<term>Muscle Weakness</term>
<term>Parkinson Disease</term>
<term>Tremor</term>
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<term>Combined Modality Therapy</term>
<term>Electrodes, Implanted</term>
<term>Humans</term>
<term>Reference Values</term>
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<p id="P1">We investigated the control of movement in 12 patients with Parkinson’s disease (PD) after they received surgically implanted high-frequency stimulating electrodes in the subthalamic nucleus (STN). The experiment studied ankle strength, movement velocity, and the associated electromyographic patterns in PD patients, six of whom had tremor at the ankle. The patients were studied
<italic>off</italic>
treatment, ON STN deep brain stimulation (DBS),
<italic>on</italic>
medication, and
<italic>on</italic>
medication plus STN DBS. Twelve matched control subjects were also examined. Medication alone and STN DBS alone increased patients’ ankle strength, ankle velocity, agonist muscle burst amplitude, and agonist burst duration, while reducing the number of agonist bursts during movement. These findings were similar for PD patients with and without tremor. The combination of medication plus STN DBS normalized maximal strength at the ankle joint, but ankle movement velocity and electromyographic patterns were not normalized. The findings are the first to demonstrate that STN DBS and medication increase strength and movement velocity at the ankle joint.</p>
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<title xml:lang="en" level="a" type="main">Effects of Deep Brain Stimulation and Medication on Strength, Bradykinesia, and Electromyographic Patterns of the Ankle Joint in Parkinson’s Disease</title>
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<name sortKey="Vaillancourt, David E" sort="Vaillancourt, David E" uniqKey="Vaillancourt D" first="David E." last="Vaillancourt">David E. Vaillancourt</name>
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<nlm:aff id="A1"> Department of Movement Science, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Movement Science, University of Illinois, Chicago, Illinois</wicri:regionArea>
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<region type="state">Illinois</region>
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<nlm:aff id="A2"> Department of Bioengineering, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Bioengineering, University of Illinois, Chicago, Illinois</wicri:regionArea>
<placeName>
<region type="state">Illinois</region>
</placeName>
</affiliation>
<affiliation wicri:level="2">
<nlm:aff id="A3"> Department of Neurology and Rehabilitation, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Neurology and Rehabilitation, University of Illinois, Chicago, Illinois</wicri:regionArea>
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<region type="state">Illinois</region>
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<author>
<name sortKey="Prodoehl, Janey" sort="Prodoehl, Janey" uniqKey="Prodoehl J" first="Janey" last="Prodoehl">Janey Prodoehl</name>
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<nlm:aff id="A1"> Department of Movement Science, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Movement Science, University of Illinois, Chicago, Illinois</wicri:regionArea>
<placeName>
<region type="state">Illinois</region>
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</affiliation>
</author>
<author>
<name sortKey="Sturman, Molly M" sort="Sturman, Molly M" uniqKey="Sturman M" first="Molly M." last="Sturman">Molly M. Sturman</name>
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<nlm:aff id="A1"> Department of Movement Science, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Movement Science, University of Illinois, Chicago, Illinois</wicri:regionArea>
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<name sortKey="Bakay, Roy A E" sort="Bakay, Roy A E" uniqKey="Bakay R" first="Roy A. E." last="Bakay">Roy A. E. Bakay</name>
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<nlm:aff id="A4"> Department of Neurosurgery, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois, USA</nlm:aff>
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<wicri:regionArea> Department of Neurosurgery, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois</wicri:regionArea>
<placeName>
<region type="state">Illinois</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Metman, Leo Verhagen" sort="Metman, Leo Verhagen" uniqKey="Metman L" first="Leo Verhagen" last="Metman">Leo Verhagen Metman</name>
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<nlm:aff id="A5"> Department of Neurological Sciences, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Neurological Sciences, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois</wicri:regionArea>
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<name sortKey="Corcos, Daniel M" sort="Corcos, Daniel M" uniqKey="Corcos D" first="Daniel M." last="Corcos">Daniel M. Corcos</name>
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<nlm:aff id="A1"> Department of Movement Science, University of Illinois, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Movement Science, University of Illinois, Chicago, Illinois</wicri:regionArea>
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<region type="state">Illinois</region>
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<affiliation wicri:level="2">
<nlm:aff id="A2"> Department of Bioengineering, University of Illinois, Chicago, Illinois, USA</nlm:aff>
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<placeName>
<region type="state">Illinois</region>
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<nlm:aff id="A5"> Department of Neurological Sciences, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Department of Neurological Sciences, Rush Presbyterian–St. Luke’s Medical Center, Chicago, Illinois</wicri:regionArea>
<placeName>
<region type="state">Illinois</region>
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<affiliation wicri:level="2">
<nlm:aff id="A6"> Department of Physical Therapy, University of Illinois, Chicago, Illinois, USA</nlm:aff>
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<wicri:regionArea> Department of Physical Therapy, University of Illinois, Chicago, Illinois</wicri:regionArea>
<placeName>
<region type="state">Illinois</region>
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</affiliation>
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<title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<idno type="eISSN">1531-8257</idno>
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<p id="P1">We investigated the control of movement in 12 patients with Parkinson’s disease (PD) after they received surgically implanted high-frequency stimulating electrodes in the subthalamic nucleus (STN). The experiment studied ankle strength, movement velocity, and the associated electromyographic patterns in PD patients, six of whom had tremor at the ankle. The patients were studied
<italic>off</italic>
treatment, ON STN deep brain stimulation (DBS),
<italic>on</italic>
medication, and
<italic>on</italic>
medication plus STN DBS. Twelve matched control subjects were also examined. Medication alone and STN DBS alone increased patients’ ankle strength, ankle velocity, agonist muscle burst amplitude, and agonist burst duration, while reducing the number of agonist bursts during movement. These findings were similar for PD patients with and without tremor. The combination of medication plus STN DBS normalized maximal strength at the ankle joint, but ankle movement velocity and electromyographic patterns were not normalized. The findings are the first to demonstrate that STN DBS and medication increase strength and movement velocity at the ankle joint.</p>
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<nlm:affiliation>Department of Movement Science, University of Illinois, Chicago, Illinois 60612, USA. court1@uic.edu</nlm:affiliation>
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<name sortKey="Bakay, Roy A E" sort="Bakay, Roy A E" uniqKey="Bakay R" first="Roy A E" last="Bakay">Roy A E. Bakay</name>
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<name sortKey="Metman, Leo Verhagen" sort="Metman, Leo Verhagen" uniqKey="Metman L" first="Leo Verhagen" last="Metman">Leo Verhagen Metman</name>
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<term>Ankle Joint (innervation)</term>
<term>Antiparkinson Agents (administration & dosage)</term>
<term>Antiparkinson Agents (adverse effects)</term>
<term>Biomechanical Phenomena</term>
<term>Carbidopa (administration & dosage)</term>
<term>Carbidopa (adverse effects)</term>
<term>Combined Modality Therapy</term>
<term>Deep Brain Stimulation (methods)</term>
<term>Electrodes, Implanted</term>
<term>Electromyography (drug effects)</term>
<term>Humans</term>
<term>Hypokinesia (physiopathology)</term>
<term>Hypokinesia (therapy)</term>
<term>Isometric Contraction (drug effects)</term>
<term>Isometric Contraction (physiology)</term>
<term>Levodopa (administration & dosage)</term>
<term>Levodopa (adverse effects)</term>
<term>Muscle Weakness (physiopathology)</term>
<term>Muscle Weakness (therapy)</term>
<term>Muscle, Skeletal (innervation)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (physiopathology)</term>
<term>Parkinson Disease (therapy)</term>
<term>Reference Values</term>
<term>Signal Processing, Computer-Assisted</term>
<term>Statistics as Topic</term>
<term>Torque</term>
<term>Treatment Outcome</term>
<term>Tremor (physiopathology)</term>
<term>Tremor (therapy)</term>
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<term>Antiparkinson Agents</term>
<term>Carbidopa</term>
<term>Levodopa</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en">
<term>Antiparkinson Agents</term>
<term>Carbidopa</term>
<term>Levodopa</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Electromyography</term>
<term>Isometric Contraction</term>
</keywords>
<keywords scheme="MESH" qualifier="innervation" xml:lang="en">
<term>Ankle Joint</term>
<term>Muscle, Skeletal</term>
</keywords>
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<term>Deep Brain Stimulation</term>
</keywords>
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<term>Isometric Contraction</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en">
<term>Hypokinesia</term>
<term>Muscle Weakness</term>
<term>Parkinson Disease</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Hypokinesia</term>
<term>Muscle Weakness</term>
<term>Parkinson Disease</term>
<term>Tremor</term>
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<term>Biomechanical Phenomena</term>
<term>Combined Modality Therapy</term>
<term>Electrodes, Implanted</term>
<term>Humans</term>
<term>Reference Values</term>
<term>Signal Processing, Computer-Assisted</term>
<term>Statistics as Topic</term>
<term>Torque</term>
<term>Treatment Outcome</term>
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<div type="abstract" xml:lang="en">We investigated the control of movement in 12 patients with Parkinson's disease (PD) after they received surgically implanted high-frequency stimulating electrodes in the subthalamic nucleus (STN). The experiment studied ankle strength, movement velocity, and the associated electromyographic patterns in PD patients, six of whom had tremor at the ankle. The patients were studied off treatment, ON STN deep brain stimulation (DBS), on medication, and on medication plus STN DBS. Twelve matched control subjects were also examined. Medication alone and STN DBS alone increased patients' ankle strength, ankle velocity, agonist muscle burst amplitude, and agonist burst duration, while reducing the number of agonist bursts during movement. These findings were similar for PD patients with and without tremor. The combination of medication plus STN DBS normalized maximal strength at the ankle joint, but ankle movement velocity and electromyographic patterns were not normalized. The findings are the first to demonstrate that STN DBS and medication increase strength and movement velocity at the ankle joint.</div>
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