Movement Disorders (revue)

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Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits

Identifieur interne : 000256 ( PascalFrancis/Corpus ); précédent : 000255; suivant : 000257

Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits

Auteurs : Ralf Reilmann ; Silke Rumpf ; Heike Beckmann ; Raphael Koch ; Erich B. Ringelstein ; Herwig W. Lange

Source :

RBID : Pascal:12-0183678

Descripteurs français

English descriptors

Abstract

Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03   1    @0 Mov. disord.
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A08 01  1  ENG  @1 Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits
A11 01  1    @1 REILMANN (Ralf)
A11 02  1    @1 RUMPF (Silke)
A11 03  1    @1 BECKMANN (Heike)
A11 04  1    @1 KOCH (Raphael)
A11 05  1    @1 RINGELSTEIN (Erich B.)
A11 06  1    @1 LANGE (Herwig W.)
A14 01      @1 Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1 @2 Muenster @3 DEU @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 5 aut. @Z 6 aut.
A14 02      @1 Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1 @2 Muenster @3 DEU @Z 4 aut.
A20       @1 555-559
A21       @1 2012
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000194678450200
A44       @0 0000 @1 © 2012 INIST-CNRS. All rights reserved.
A45       @0 19 ref.
A47 01  1    @0 12-0183678
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
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C03 01  X  ENG  @0 Huntington disease @5 01
C03 01  X  SPA  @0 Corea Huntington @5 01
C03 02  X  FRE  @0 Trouble moteur @5 02
C03 02  X  ENG  @0 Motor system disorder @5 02
C03 02  X  SPA  @0 Trastorno motor @5 02
C03 03  X  FRE  @0 Déficit fonctionnel @5 03
C03 03  X  ENG  @0 Functional deficit @5 03
C03 03  X  SPA  @0 Deficiencia funcional @5 03
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C03 04  X  SPA  @0 Sistema nervioso patología @5 04
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C03 05  X  ENG  @0 Posture @5 09
C03 05  X  SPA  @0 Postura @5 09
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C03 06  X  ENG  @0 Prognosis @5 10
C03 06  X  SPA  @0 Pronóstico @5 10
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C03 07  X  ENG  @0 Motor control @5 11
C03 07  X  SPA  @0 Control motor @5 11
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C03 08  X  ENG  @0 Basal ganglion @5 12
C03 08  X  SPA  @0 Núcleo basal @5 12
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C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Maladie héréditaire @5 40
C07 04  X  ENG  @0 Genetic disease @5 40
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C07 05  X  ENG  @0 Central nervous system disease @5 41
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Format Inist (serveur)

NO : PASCAL 12-0183678 INIST
ET : Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits
AU : REILMANN (Ralf); RUMPF (Silke); BECKMANN (Heike); KOCH (Raphael); RINGELSTEIN (Erich B.); LANGE (Herwig W.)
AF : Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (4 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2012; Vol. 27; No. 4; Pp. 555-559; Bibl. 19 ref.
LA : Anglais
EA : Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.
CC : 002B17; 002B17G
FD : Chorée de Huntington; Trouble moteur; Déficit fonctionnel; Pathologie du système nerveux; Posture; Pronostic; Contrôle moteur; Noyau gris central
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Maladie héréditaire; Pathologie du système nerveux central; Trouble neurologique; Encéphale; Système nerveux central
ED : Huntington disease; Motor system disorder; Functional deficit; Nervous system diseases; Posture; Prognosis; Motor control; Basal ganglion
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Central nervous system disease; Neurological disorder; Encephalon; Central nervous system
SD : Corea Huntington; Trastorno motor; Deficiencia funcional; Sistema nervioso patología; Postura; Pronóstico; Control motor; Núcleo basal
LO : INIST-20953.354000194678450200
ID : 12-0183678

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Pascal:12-0183678

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<div type="abstract" xml:lang="en">Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.</div>
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<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Huntington disease</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Corea Huntington</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Trouble moteur</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Motor system disorder</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Trastorno motor</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Déficit fonctionnel</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Functional deficit</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Deficiencia funcional</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Pathologie du système nerveux</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Posture</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Posture</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Postura</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Pronostic</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Prognosis</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Pronóstico</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Contrôle moteur</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Motor control</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Control motor</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Noyau gris central</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Basal ganglion</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Núcleo basal</s0>
<s5>12</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Pathologie de l'encéphale</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Syndrome extrapyramidal</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Maladie héréditaire</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Genetic disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Enfermedad hereditaria</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Pathologie du système nerveux central</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Encéphale</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Encephalon</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Encéfalo</s0>
<s5>44</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Système nerveux central</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Central nervous system</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Sistema nervioso central</s0>
<s5>45</s5>
</fC07>
<fN21>
<s1>142</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 12-0183678 INIST</NO>
<ET>Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits</ET>
<AU>REILMANN (Ralf); RUMPF (Silke); BECKMANN (Heike); KOCH (Raphael); RINGELSTEIN (Erich B.); LANGE (Herwig W.)</AU>
<AF>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (4 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2012; Vol. 27; No. 4; Pp. 555-559; Bibl. 19 ref.</SO>
<LA>Anglais</LA>
<EA>Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.</EA>
<CC>002B17; 002B17G</CC>
<FD>Chorée de Huntington; Trouble moteur; Déficit fonctionnel; Pathologie du système nerveux; Posture; Pronostic; Contrôle moteur; Noyau gris central</FD>
<FG>Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Maladie héréditaire; Pathologie du système nerveux central; Trouble neurologique; Encéphale; Système nerveux central</FG>
<ED>Huntington disease; Motor system disorder; Functional deficit; Nervous system diseases; Posture; Prognosis; Motor control; Basal ganglion</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Central nervous system disease; Neurological disorder; Encephalon; Central nervous system</EG>
<SD>Corea Huntington; Trastorno motor; Deficiencia funcional; Sistema nervioso patología; Postura; Pronóstico; Control motor; Núcleo basal</SD>
<LO>INIST-20953.354000194678450200</LO>
<ID>12-0183678</ID>
</server>
</inist>
</record>

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