Short-term variability in amplitude and motor topography of whole-body involuntary movements in Parkinson's disease dyskinesias and in Huntington's chorea
Identifieur interne : 002380 ( Main/Curation ); précédent : 002379; suivant : 002381Short-term variability in amplitude and motor topography of whole-body involuntary movements in Parkinson's disease dyskinesias and in Huntington's chorea
Auteurs : Alison Fenney [Canada] ; Mandar S. Jog [Canada] ; Christian Duval [Canada]Source :
- Clinical neurology and neurosurgery [ 0303-8467 ] ; 2008.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Chirurgie.
English descriptors
- KwdEn :
- Aged, Amplitude, Antiparkinson Agents (adverse effects), Arm, Body movement, Chorea, Cohort Studies, Dyskinesia, Dyskinesia, Drug-Induced (etiology), Dyskinesia, Drug-Induced (physiopathology), Female, Humans, Huntington Disease (physiopathology), Huntington disease, Involuntary movement, Leg, Levodopa (adverse effects), Male, Middle Aged, Nervous system diseases, Parkinson Disease (drug therapy), Parkinson Disease (physiopathology), Parkinson disease, Posture (physiology), Short term, Surgery, Thorax, Time Factors, Topography, Variability.
- MESH :
- chemical , adverse effects : Antiparkinson Agents, Levodopa.
- drug therapy : Parkinson Disease.
- etiology : Dyskinesia, Drug-Induced.
- physiology : Posture.
- physiopathology : Dyskinesia, Drug-Induced, Huntington Disease, Parkinson Disease.
- Aged, Arm, Cohort Studies, Female, Humans, Leg, Male, Middle Aged, Thorax, Time Factors.
Abstract
Objectives: Clinical observations have noted variability in amplitude of levodopa-induced dyskinesias (LID) in Parkinson's disease (PD) and chorea in Huntington's disease (HD) during the day. However, no studies have examined whether both the amplitude and body location (motor topography) of whole-body involuntary movement (WBIM) varied over short periods of time (seconds or minutes), which may have a distinct and significant effect on how disruptive these WBIM may be. The present study quantified the variability of WBIM amplitude and motor topography in patients with PD having LID and in patients with HD having chorea. Patients and methods: WBIM was quantified using the MotionMonitor<TM> magnetic motion tracker system. Five patients in each group were tested in two conditions: sitting and standing. Results: WBIM increased from sitting to standing, more so in choreic patients. WBIM varied from 17% to 102% of total WBIM amplitude. Chorea tended to present with greater variability than LID in absolute terms in the standing condition, but not when the mean WBIM amplitude was taken into consideration. Motor topography of WBIM also varied more in the HD group, but mostly in the seated condition where more limbs were free to move. Neither group expressed any laterality of involuntary movement, with amplitude being equally distributed on both sides of the body. Conclusion: Results show significant short-term variability in amplitude of chorea and LID, as well as, variability in location of these involuntary movements, illustrating the complexity of the adaptations required to live and be active with involuntary movements such as HD chorea or PD dyskinesias.
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Pascal:08-0107040Le document en format XML
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<term>Chorea</term>
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<term>Dyskinesia</term>
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<term>Male</term>
<term>Middle Aged</term>
<term>Thorax</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Mouvement involontaire</term>
<term>Maladie de Parkinson</term>
<term>Chorée de Huntington</term>
<term>Dyskinésie</term>
<term>Syndrome choréique</term>
<term>Pathologie du système nerveux</term>
<term>Court terme</term>
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<term>Amplitude</term>
<term>Topographie</term>
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<front><div type="abstract" xml:lang="en">Objectives: Clinical observations have noted variability in amplitude of levodopa-induced dyskinesias (LID) in Parkinson's disease (PD) and chorea in Huntington's disease (HD) during the day. However, no studies have examined whether both the amplitude and body location (motor topography) of whole-body involuntary movement (WBIM) varied over short periods of time (seconds or minutes), which may have a distinct and significant effect on how disruptive these WBIM may be. The present study quantified the variability of WBIM amplitude and motor topography in patients with PD having LID and in patients with HD having chorea. Patients and methods: WBIM was quantified using the MotionMonitor<<sup>TM</sup>
> magnetic motion tracker system. Five patients in each group were tested in two conditions: sitting and standing. Results: WBIM increased from sitting to standing, more so in choreic patients. WBIM varied from 17% to 102% of total WBIM amplitude. Chorea tended to present with greater variability than LID in absolute terms in the standing condition, but not when the mean WBIM amplitude was taken into consideration. Motor topography of WBIM also varied more in the HD group, but mostly in the seated condition where more limbs were free to move. Neither group expressed any laterality of involuntary movement, with amplitude being equally distributed on both sides of the body. Conclusion: Results show significant short-term variability in amplitude of chorea and LID, as well as, variability in location of these involuntary movements, illustrating the complexity of the adaptations required to live and be active with involuntary movements such as HD chorea or PD dyskinesias.</div>
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<term>Huntington disease</term>
<term>Involuntary movement</term>
<term>Nervous system diseases</term>
<term>Parkinson disease</term>
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<term>Variability</term>
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<term>Maladie de Parkinson</term>
<term>Chorée de Huntington</term>
<term>Dyskinésie</term>
<term>Syndrome choréique</term>
<term>Pathologie du système nerveux</term>
<term>Court terme</term>
<term>Variabilité</term>
<term>Amplitude</term>
<term>Topographie</term>
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<front><div type="abstract" xml:lang="en">Objectives: Clinical observations have noted variability in amplitude of levodopa-induced dyskinesias (LID) in Parkinson's disease (PD) and chorea in Huntington's disease (HD) during the day. However, no studies have examined whether both the amplitude and body location (motor topography) of whole-body involuntary movement (WBIM) varied over short periods of time (seconds or minutes), which may have a distinct and significant effect on how disruptive these WBIM may be. The present study quantified the variability of WBIM amplitude and motor topography in patients with PD having LID and in patients with HD having chorea. Patients and methods: WBIM was quantified using the MotionMonitor<<sup>TM</sup>
> magnetic motion tracker system. Five patients in each group were tested in two conditions: sitting and standing. Results: WBIM increased from sitting to standing, more so in choreic patients. WBIM varied from 17% to 102% of total WBIM amplitude. Chorea tended to present with greater variability than LID in absolute terms in the standing condition, but not when the mean WBIM amplitude was taken into consideration. Motor topography of WBIM also varied more in the HD group, but mostly in the seated condition where more limbs were free to move. Neither group expressed any laterality of involuntary movement, with amplitude being equally distributed on both sides of the body. Conclusion: Results show significant short-term variability in amplitude of chorea and LID, as well as, variability in location of these involuntary movements, illustrating the complexity of the adaptations required to live and be active with involuntary movements such as HD chorea or PD dyskinesias.</div>
</front>
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<orgName type="university">Université du Québec à Montréal</orgName>
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<author><name sortKey="Jog, Mandar S" sort="Jog, Mandar S" uniqKey="Jog M" first="Mandar S" last="Jog">Mandar S. Jog</name>
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<author><name sortKey="Duval, Christian" sort="Duval, Christian" uniqKey="Duval C" first="Christian" last="Duval">Christian Duval</name>
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<idno type="RBID">pubmed:18063471</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Short-term variability in amplitude and motor topography of whole-body involuntary movements in Parkinson's disease dyskinesias and in Huntington's chorea.</title>
<author><name sortKey="Fenney, Alison" sort="Fenney, Alison" uniqKey="Fenney A" first="Alison" last="Fenney">Alison Fenney</name>
<affiliation wicri:level="4"><nlm:affiliation>Département de Kinanthropologie, Université du Québec à Montréal, C.P. 8888, Succursale Centre-Ville, Montréal, Québec, Canada H3C 3P8.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>Département de Kinanthropologie, Université du Québec à Montréal, C.P. 8888, Succursale Centre-Ville, Montréal, Québec</wicri:regionArea>
<orgName type="university">Université du Québec à Montréal</orgName>
<placeName><settlement type="city">Montréal</settlement>
<region type="state">Québec</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jog, Mandar S" sort="Jog, Mandar S" uniqKey="Jog M" first="Mandar S" last="Jog">Mandar S. Jog</name>
</author>
<author><name sortKey="Duval, Christian" sort="Duval, Christian" uniqKey="Duval C" first="Christian" last="Duval">Christian Duval</name>
</author>
</analytic>
<series><title level="j">Clinical neurology and neurosurgery</title>
<idno type="ISSN">0303-8467</idno>
<imprint><date when="2008" type="published">2008</date>
</imprint>
</series>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Antiparkinson Agents (adverse effects)</term>
<term>Arm</term>
<term>Cohort Studies</term>
<term>Dyskinesia, Drug-Induced (etiology)</term>
<term>Dyskinesia, Drug-Induced (physiopathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Huntington Disease (physiopathology)</term>
<term>Leg</term>
<term>Levodopa (adverse effects)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (drug therapy)</term>
<term>Parkinson Disease (physiopathology)</term>
<term>Posture (physiology)</term>
<term>Thorax</term>
<term>Time Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en"><term>Antiparkinson Agents</term>
<term>Levodopa</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dyskinesia, Drug-Induced</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Posture</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Dyskinesia, Drug-Induced</term>
<term>Huntington Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Arm</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Leg</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Thorax</term>
<term>Time Factors</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Clinical observations have noted variability in amplitude of levodopa-induced dyskinesias (LID) in Parkinson's disease (PD) and chorea in Huntington's disease (HD) during the day. However, no studies have examined whether both the amplitude and body location (motor topography) of whole-body involuntary movement (WBIM) varied over short periods of time (seconds or minutes), which may have a distinct and significant effect on how disruptive these WBIM may be. The present study quantified the variability of WBIM amplitude and motor topography in patients with PD having LID and in patients with HD having chorea.</div>
</front>
</TEI>
</PubMed>
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