Movement Disorders (revue)

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Effects of pallidotomy and levodopa on walking and reaching movements in Parkinson's disease

Identifieur interne : 002394 ( PascalFrancis/Corpus ); précédent : 002393; suivant : 002395

Effects of pallidotomy and levodopa on walking and reaching movements in Parkinson's disease

Auteurs : Amy J. Bastian ; Valerie E. Kelly ; Joel S. Perlmutter ; Jonathan W. Mink

Source :

RBID : Pascal:04-0052798

Descripteurs français

English descriptors

Abstract

We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.

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Pour connaître la documentation sur le format Inist Standard.

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A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 18
A06       @2 9
A08 01  1  ENG  @1 Effects of pallidotomy and levodopa on walking and reaching movements in Parkinson's disease
A11 01  1    @1 BASTIAN (Amy J.)
A11 02  1    @1 KELLY (Valerie E.)
A11 03  1    @1 PERLMUTTER (Joel S.)
A11 04  1    @1 MINK (Jonathan W.)
A14 01      @1 Kennedy Krieger Institute @2 Baltimore, Maryland @3 USA @Z 1 aut.
A14 02      @1 Program in Physical Therapy, Washington University @2 St. Louis, Missouri @3 USA @Z 1 aut. @Z 2 aut.
A14 03      @1 Departments of Neurology, Radiology, and Anatomy & Neurobiology, Washington University @2 St. Louis, Missouri @3 USA @Z 3 aut.
A14 04      @1 Departments of Neurology (Child Neurology), Neurobiology & Anatomy, and Pediatrics, University of Rochester @2 Rochester, New York @3 USA @Z 4 aut.
A14 05      @1 Department of Neurology, Johns Hopkins @2 Baltimore, Maryland @3 USA
A20       @1 1008-1017
A21       @1 2003
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000113072050060
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
A45       @0 40 ref.
A47 01  1    @0 04-0052798
A60       @1 P
A61       @0 A
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C01 01    ENG  @0 We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.
C02 01  X    @0 002B02B06
C02 02  X    @0 002B25J01
C03 01  X  FRE  @0 Parkinson maladie @5 01
C03 01  X  ENG  @0 Parkinson disease @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @5 01
C03 02  X  FRE  @0 Lévodopa @2 NK @2 FR @5 04
C03 02  X  ENG  @0 Levodopa @2 NK @2 FR @5 04
C03 02  X  SPA  @0 Levodopa @2 NK @2 FR @5 04
C03 03  X  FRE  @0 Chimiothérapie @5 05
C03 03  X  ENG  @0 Chemotherapy @5 05
C03 03  X  SPA  @0 Quimioterapia @5 05
C03 04  X  FRE  @0 Pallidum @5 07
C03 04  X  ENG  @0 Pallidum @5 07
C03 04  X  SPA  @0 Pallidum @5 07
C03 05  X  FRE  @0 Exérèse @5 08
C03 05  X  ENG  @0 Exeresis @5 08
C03 05  X  SPA  @0 Exéresis @5 08
C03 06  X  FRE  @0 Unilatéral @5 09
C03 06  X  ENG  @0 Unilateral @5 09
C03 06  X  SPA  @0 Unilateral @5 09
C03 07  X  FRE  @0 Marche à pied @5 10
C03 07  X  ENG  @0 Walking @5 10
C03 07  X  SPA  @0 Caminata @5 10
C03 08  X  FRE  @0 Mouvement corporel @5 11
C03 08  X  ENG  @0 Body movement @5 11
C03 08  X  SPA  @0 Movimiento corporal @5 11
C03 09  X  FRE  @0 Atteignabilité @5 12
C03 09  X  ENG  @0 Reachability @5 12
C03 09  X  SPA  @0 Asequibilidad @5 12
C03 10  X  FRE  @0 Cinématique @5 13
C03 10  X  ENG  @0 Kinematics @5 13
C03 10  X  SPA  @0 Cinemática @5 13
C03 11  X  FRE  @0 Traitement associé @5 17
C03 11  X  ENG  @0 Combined treatment @5 17
C03 11  X  SPA  @0 Tratamiento asociado @5 17
C03 12  X  FRE  @0 Pronostic @5 18
C03 12  X  ENG  @0 Prognosis @5 18
C03 12  X  SPA  @0 Pronóstico @5 18
C03 13  X  FRE  @0 Adulte @5 20
C03 13  X  ENG  @0 Adult @5 20
C03 13  X  SPA  @0 Adulto @5 20
C07 01  X  FRE  @0 Homme
C07 01  X  ENG  @0 Human
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C07 02  X  FRE  @0 Système nerveux pathologie @5 37
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C07 05  X  FRE  @0 Extrapyramidal syndrome @5 40
C07 05  X  ENG  @0 Extrapyramidal syndrome @5 40
C07 05  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 06  X  FRE  @0 Maladie dégénérative @5 41
C07 06  X  ENG  @0 Degenerative disease @5 41
C07 06  X  SPA  @0 Enfermedad degenerativa @5 41
C07 07  X  FRE  @0 Antiparkinsonien @5 45
C07 07  X  ENG  @0 Antiparkinson agent @5 45
C07 07  X  SPA  @0 Antiparkinsoniano @5 45
C07 08  X  FRE  @0 Chirurgie @5 53
C07 08  X  ENG  @0 Surgery @5 53
C07 08  X  SPA  @0 Cirugía @5 53
N21       @1 033
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Format Inist (serveur)

NO : PASCAL 04-0052798 INIST
ET : Effects of pallidotomy and levodopa on walking and reaching movements in Parkinson's disease
AU : BASTIAN (Amy J.); KELLY (Valerie E.); PERLMUTTER (Joel S.); MINK (Jonathan W.)
AF : Kennedy Krieger Institute/Baltimore, Maryland/Etats-Unis (1 aut.); Program in Physical Therapy, Washington University/St. Louis, Missouri/Etats-Unis (1 aut., 2 aut.); Departments of Neurology, Radiology, and Anatomy & Neurobiology, Washington University/St. Louis, Missouri/Etats-Unis (3 aut.); Departments of Neurology (Child Neurology), Neurobiology & Anatomy, and Pediatrics, University of Rochester/Rochester, New York/Etats-Unis (4 aut.); Department of Neurology, Johns Hopkins/Baltimore, Maryland/Etats-Unis
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2003; Vol. 18; No. 9; Pp. 1008-1017; Bibl. 40 ref.
LA : Anglais
EA : We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.
CC : 002B02B06; 002B25J01
FD : Parkinson maladie; Lévodopa; Chimiothérapie; Pallidum; Exérèse; Unilatéral; Marche à pied; Mouvement corporel; Atteignabilité; Cinématique; Traitement associé; Pronostic; Adulte
FG : Homme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Antiparkinsonien; Chirurgie
ED : Parkinson disease; Levodopa; Chemotherapy; Pallidum; Exeresis; Unilateral; Walking; Body movement; Reachability; Kinematics; Combined treatment; Prognosis; Adult
EG : Human; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Antiparkinson agent; Surgery
SD : Parkinson enfermedad; Levodopa; Quimioterapia; Pallidum; Exéresis; Unilateral; Caminata; Movimiento corporal; Asequibilidad; Cinemática; Tratamiento asociado; Pronóstico; Adulto
LO : INIST-20953.354000113072050060
ID : 04-0052798

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Pascal:04-0052798

Le document en format XML

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<div type="abstract" xml:lang="en">We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.</div>
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<s0>We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B02B06</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B25J01</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Parkinson maladie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Parkinson disease</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Parkinson enfermedad</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Lévodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Chimiothérapie</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Chemotherapy</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Quimioterapia</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Pallidum</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Pallidum</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Pallidum</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Exérèse</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Exeresis</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Exéresis</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Unilatéral</s0>
<s5>09</s5>
</fC03>
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<s0>Unilateral</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
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<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Marche à pied</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Walking</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Caminata</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Mouvement corporel</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Body movement</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Movimiento corporal</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Atteignabilité</s0>
<s5>12</s5>
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<fC03 i1="09" i2="X" l="ENG">
<s0>Reachability</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Asequibilidad</s0>
<s5>12</s5>
</fC03>
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<s0>Cinématique</s0>
<s5>13</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Kinematics</s0>
<s5>13</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Cinemática</s0>
<s5>13</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Traitement associé</s0>
<s5>17</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Combined treatment</s0>
<s5>17</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Tratamiento asociado</s0>
<s5>17</s5>
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<s5>18</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
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<s5>18</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Pronóstico</s0>
<s5>18</s5>
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<s0>Adulte</s0>
<s5>20</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Adult</s0>
<s5>20</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Adulto</s0>
<s5>20</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Homme</s0>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Human</s0>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Hombre</s0>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Antiparkinsonien</s0>
<s5>45</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Antiparkinson agent</s0>
<s5>45</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Antiparkinsoniano</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Chirurgie</s0>
<s5>53</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Surgery</s0>
<s5>53</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Cirugía</s0>
<s5>53</s5>
</fC07>
<fN21>
<s1>033</s1>
</fN21>
<fN82>
<s1>PSI</s1>
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<NO>PASCAL 04-0052798 INIST</NO>
<ET>Effects of pallidotomy and levodopa on walking and reaching movements in Parkinson's disease</ET>
<AU>BASTIAN (Amy J.); KELLY (Valerie E.); PERLMUTTER (Joel S.); MINK (Jonathan W.)</AU>
<AF>Kennedy Krieger Institute/Baltimore, Maryland/Etats-Unis (1 aut.); Program in Physical Therapy, Washington University/St. Louis, Missouri/Etats-Unis (1 aut., 2 aut.); Departments of Neurology, Radiology, and Anatomy & Neurobiology, Washington University/St. Louis, Missouri/Etats-Unis (3 aut.); Departments of Neurology (Child Neurology), Neurobiology & Anatomy, and Pediatrics, University of Rochester/Rochester, New York/Etats-Unis (4 aut.); Department of Neurology, Johns Hopkins/Baltimore, Maryland/Etats-Unis</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2003; Vol. 18; No. 9; Pp. 1008-1017; Bibl. 40 ref.</SO>
<LA>Anglais</LA>
<EA>We examined the effects of levodopa and unilateral pallidotomy on quantitative measures of walking and reaching in Parkinson's disease (PD). We also compared quantitative measures of movement with standard clinical rating scales. We used kinematic measures and the Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale (subscale III) to evaluate the movement of 10 people with PD. Subjects were tested after withholding PD medications for at least 8 hours and again 30 to 45 minutes after taking the first morning dose of levodopa. They were studied in this manner before unilateral pallidotomy and then 3.5 to 10 months after surgery. The UPDRS motor subscale was performed in each state. Kinematic data were collected as subjects reached to a target and walked. The UPDRS motor subscale ratings were similar to those reported in the literature: pallidotomy improved the overall motor score and the contralateral bradykinesia + rigidity score, but not the gait + posture score. In contrast, kinematic measures demonstrated that levodopa and pallidotomy had different effects on walking and reaching speed. Both treatments improved walking speed, and the effect was additive. Levodopa improved reaching speed before pallidotomy but did not improve it as much after pallidotomy. Additionally, pallidotomy had inconsistent effects on reaching; some subjects were faster and others were slower. The subjects who initially reached more slowly improved after pallidotomy; the subjects who initially reached more normally (faster) worsened after pallidotomy. On the basis of our results, we speculate that basal ganglia output pathways that control walking and reaching may be distinct. such that bilateral projections to the pedunculopontine area influence walking, whereas ipsilateral thalamocortical projections influence reaching.</EA>
<CC>002B02B06; 002B25J01</CC>
<FD>Parkinson maladie; Lévodopa; Chimiothérapie; Pallidum; Exérèse; Unilatéral; Marche à pied; Mouvement corporel; Atteignabilité; Cinématique; Traitement associé; Pronostic; Adulte</FD>
<FG>Homme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Antiparkinsonien; Chirurgie</FG>
<ED>Parkinson disease; Levodopa; Chemotherapy; Pallidum; Exeresis; Unilateral; Walking; Body movement; Reachability; Kinematics; Combined treatment; Prognosis; Adult</ED>
<EG>Human; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Antiparkinson agent; Surgery</EG>
<SD>Parkinson enfermedad; Levodopa; Quimioterapia; Pallidum; Exéresis; Unilateral; Caminata; Movimiento corporal; Asequibilidad; Cinemática; Tratamiento asociado; Pronóstico; Adulto</SD>
<LO>INIST-20953.354000113072050060</LO>
<ID>04-0052798</ID>
</server>
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