Movement Disorders (revue)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Trunk sway in patients with spinocerebellar ataxia

Identifieur interne : 001E07 ( PascalFrancis/Corpus ); précédent : 001E06; suivant : 001E08

Trunk sway in patients with spinocerebellar ataxia

Auteurs : Bart P. C. Van De Warrenburg ; Maaike Bakker ; Berry P. H. Kremer ; Bastiaan R. Bloem ; John H. J. Allum

Source :

RBID : Pascal:05-0444031

Descripteurs français

English descriptors

Abstract

We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 20
A06       @2 8
A08 01  1  ENG  @1 Trunk sway in patients with spinocerebellar ataxia
A11 01  1    @1 VAN DE WARRENBURG (Bart P. C.)
A11 02  1    @1 BAKKER (Maaike)
A11 03  1    @1 KREMER (Berry P. H.)
A11 04  1    @1 BLOEM (Bastiaan R.)
A11 05  1    @1 ALLUM (John H. J.)
A14 01      @1 Department of Neurology, University Medical Center Nijmegen @3 NLD @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.
A14 02      @1 Department of Otorhinolaryngology, University Hospital Basel @3 CHE @Z 2 aut. @Z 5 aut.
A20       @1 1006-1013
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000132711360150
A44       @0 0000 @1 © 2005 INIST-CNRS. All rights reserved.
A45       @0 16 ref.
A47 01  1    @0 05-0444031
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.
C02 01  X    @0 002B17
C02 02  X    @0 002B17F
C02 03  X    @0 002B17G
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Tronc @5 09
C03 02  X  ENG  @0 Trunk @5 09
C03 02  X  SPA  @0 Tronco @5 09
C03 03  X  FRE  @0 Homme @5 10
C03 03  X  ENG  @0 Human @5 10
C03 03  X  SPA  @0 Hombre @5 10
C03 04  X  FRE  @0 Ataxie spinocérébelleuse @2 NM @5 11
C03 04  X  ENG  @0 Spinocerebellar ataxia @2 NM @5 11
C03 04  X  SPA  @0 Ataxia spinocerebelosa @2 NM @5 11
C03 05  X  FRE  @0 Ataxie cérébelleuse @2 NM @5 12
C03 05  X  ENG  @0 Cerebellar ataxia @2 NM @5 12
C03 05  X  SPA  @0 Ataxia cerebelosa @2 NM @5 12
C03 06  X  FRE  @0 Posturographie @5 13
C03 06  X  ENG  @0 Posturography @5 13
C03 06  X  SPA  @0 Posturografía @5 13
C07 01  X  FRE  @0 Maladie dégénérative @5 37
C07 01  X  ENG  @0 Degenerative disease @5 37
C07 01  X  SPA  @0 Enfermedad degenerativa @5 37
C07 02  X  FRE  @0 Maladie héréditaire @5 38
C07 02  X  ENG  @0 Genetic disease @5 38
C07 02  X  SPA  @0 Enfermedad hereditaria @5 38
C07 03  X  FRE  @0 Système nerveux central pathologie @5 39
C07 03  X  ENG  @0 Central nervous system disease @5 39
C07 03  X  SPA  @0 Sistema nervosio central patología @5 39
N21       @1 311
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 05-0444031 INIST
ET : Trunk sway in patients with spinocerebellar ataxia
AU : VAN DE WARRENBURG (Bart P. C.); BAKKER (Maaike); KREMER (Berry P. H.); BLOEM (Bastiaan R.); ALLUM (John H. J.)
AF : Department of Neurology, University Medical Center Nijmegen/Pays-Bas (1 aut., 2 aut., 3 aut., 4 aut.); Department of Otorhinolaryngology, University Hospital Basel/Suisse (2 aut., 5 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. 8; Pp. 1006-1013; Bibl. 16 ref.
LA : Anglais
EA : We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.
CC : 002B17; 002B17F; 002B17G
FD : Système nerveux pathologie; Tronc; Homme; Ataxie spinocérébelleuse; Ataxie cérébelleuse; Posturographie
FG : Maladie dégénérative; Maladie héréditaire; Système nerveux central pathologie
ED : Nervous system diseases; Trunk; Human; Spinocerebellar ataxia; Cerebellar ataxia; Posturography
EG : Degenerative disease; Genetic disease; Central nervous system disease
SD : Sistema nervioso patología; Tronco; Hombre; Ataxia spinocerebelosa; Ataxia cerebelosa; Posturografía
LO : INIST-20953.354000132711360150
ID : 05-0444031

Links to Exploration step

Pascal:05-0444031

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Trunk sway in patients with spinocerebellar ataxia</title>
<author>
<name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Bakker, Maaike" sort="Bakker, Maaike" uniqKey="Bakker M" first="Maaike" last="Bakker">Maaike Bakker</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Otorhinolaryngology, University Hospital Basel</s1>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Kremer, Berry P H" sort="Kremer, Berry P H" uniqKey="Kremer B" first="Berry P. H." last="Kremer">Berry P. H. Kremer</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Bloem, Bastiaan R" sort="Bloem, Bastiaan R" uniqKey="Bloem B" first="Bastiaan R." last="Bloem">Bastiaan R. Bloem</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Allum, John H J" sort="Allum, John H J" uniqKey="Allum J" first="John H. J." last="Allum">John H. J. Allum</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Otorhinolaryngology, University Hospital Basel</s1>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">05-0444031</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 05-0444031 INIST</idno>
<idno type="RBID">Pascal:05-0444031</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001E07</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Trunk sway in patients with spinocerebellar ataxia</title>
<author>
<name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Bakker, Maaike" sort="Bakker, Maaike" uniqKey="Bakker M" first="Maaike" last="Bakker">Maaike Bakker</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Otorhinolaryngology, University Hospital Basel</s1>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Kremer, Berry P H" sort="Kremer, Berry P H" uniqKey="Kremer B" first="Berry P. H." last="Kremer">Berry P. H. Kremer</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Bloem, Bastiaan R" sort="Bloem, Bastiaan R" uniqKey="Bloem B" first="Bastiaan R." last="Bloem">Bastiaan R. Bloem</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Allum, John H J" sort="Allum, John H J" uniqKey="Allum J" first="John H. J." last="Allum">John H. J. Allum</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Otorhinolaryngology, University Hospital Basel</s1>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2005">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Cerebellar ataxia</term>
<term>Human</term>
<term>Nervous system diseases</term>
<term>Posturography</term>
<term>Spinocerebellar ataxia</term>
<term>Trunk</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Système nerveux pathologie</term>
<term>Tronc</term>
<term>Homme</term>
<term>Ataxie spinocérébelleuse</term>
<term>Ataxie cérébelleuse</term>
<term>Posturographie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.</div>
</front>
</TEI>
<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0885-3185</s0>
</fA01>
<fA03 i2="1">
<s0>Mov. disord.</s0>
</fA03>
<fA05>
<s2>20</s2>
</fA05>
<fA06>
<s2>8</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Trunk sway in patients with spinocerebellar ataxia</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>VAN DE WARRENBURG (Bart P. C.)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>BAKKER (Maaike)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>KREMER (Berry P. H.)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>BLOEM (Bastiaan R.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>ALLUM (John H. J.)</s1>
</fA11>
<fA14 i1="01">
<s1>Department of Neurology, University Medical Center Nijmegen</s1>
<s3>NLD</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Department of Otorhinolaryngology, University Hospital Basel</s1>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA20>
<s1>1006-1013</s1>
</fA20>
<fA21>
<s1>2005</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>20953</s2>
<s5>354000132711360150</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2005 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>16 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>05-0444031</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Movement disorders</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B17F</s0>
</fC02>
<fC02 i1="03" i2="X">
<s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Tronc</s0>
<s5>09</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Trunk</s0>
<s5>09</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Tronco</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Homme</s0>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Human</s0>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Ataxie spinocérébelleuse</s0>
<s2>NM</s2>
<s5>11</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Spinocerebellar ataxia</s0>
<s2>NM</s2>
<s5>11</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Ataxia spinocerebelosa</s0>
<s2>NM</s2>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Ataxie cérébelleuse</s0>
<s2>NM</s2>
<s5>12</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Cerebellar ataxia</s0>
<s2>NM</s2>
<s5>12</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Ataxia cerebelosa</s0>
<s2>NM</s2>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Posturographie</s0>
<s5>13</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Posturography</s0>
<s5>13</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Posturografía</s0>
<s5>13</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Maladie héréditaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Genetic disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Enfermedad hereditaria</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>39</s5>
</fC07>
<fN21>
<s1>311</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 05-0444031 INIST</NO>
<ET>Trunk sway in patients with spinocerebellar ataxia</ET>
<AU>VAN DE WARRENBURG (Bart P. C.); BAKKER (Maaike); KREMER (Berry P. H.); BLOEM (Bastiaan R.); ALLUM (John H. J.)</AU>
<AF>Department of Neurology, University Medical Center Nijmegen/Pays-Bas (1 aut., 2 aut., 3 aut., 4 aut.); Department of Otorhinolaryngology, University Hospital Basel/Suisse (2 aut., 5 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. 8; Pp. 1006-1013; Bibl. 16 ref.</SO>
<LA>Anglais</LA>
<EA>We investigated whether quantified measurements of trunk sway during stance and gait tests in patients with autosomal dominant spinocerebellar ataxia (SCA) could be a useful approach to assess ataxia, which is highly relevant for adequate follow-up and future intervention studies. Examined were 11 SCA patients and 11 age-matched, healthy controls. Postural and balance control were quantified using peak-to-peak measurements of trunk angle and angular velocity, in the roll (lateral) and pitch (anterior-posterior) directions, during a battery of stance and gait tasks. In all stance tasks, trunk angle displacement and angular velocity in both the pitch and roll planes were significantly larger in the SCA group compared with the control group. Among the ataxia patients instability was more increased in the pitch than in the roll direction for two-legged stance tasks, especially when standing on foam, with pronounced oscillations in the pitch plane at 1.4 and 2.5 Hz. A similar dominance of pitch over roll instability was also observed in most gait tasks, especially for tandem gait and while walking with simultaneous head rotations. Trunk sway measurements were effective in detecting and quantifying the gait and balance abnormalities in SCA patients, suggesting that this method might be used for follow-up studies of SCA patients. Furthermore, the method might help to identify early symptomatic individuals and those patients at risk of falling. The postural instability in SCA was found to be multidirectional, although there is generally more pitch than roll instability corresponding with predominant involvement of the spinocerebellum.</EA>
<CC>002B17; 002B17F; 002B17G</CC>
<FD>Système nerveux pathologie; Tronc; Homme; Ataxie spinocérébelleuse; Ataxie cérébelleuse; Posturographie</FD>
<FG>Maladie dégénérative; Maladie héréditaire; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Trunk; Human; Spinocerebellar ataxia; Cerebellar ataxia; Posturography</ED>
<EG>Degenerative disease; Genetic disease; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Tronco; Hombre; Ataxia spinocerebelosa; Ataxia cerebelosa; Posturografía</SD>
<LO>INIST-20953.354000132711360150</LO>
<ID>05-0444031</ID>
</server>
</inist>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PascalFrancis/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001E07 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 001E07 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    PascalFrancis
   |étape=   Corpus
   |type=    RBID
   |clé=     Pascal:05-0444031
   |texte=   Trunk sway in patients with spinocerebellar ataxia
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024