MovDisordV3, Main, Curation, bibRecord, 003435

Eye–hand coordination in essential tremor

Identifieur interne : 003435 ( Main/Curation ); précédent : 003434; suivant : 003436

Eye–hand coordination in essential tremor

Auteurs : Peter Trillenberg [Allemagne] ; Julia Führer [Allemagne] ; Andreas Sprenger [Allemagne] ; Ania Hagenow [Allemagne] ; Detlef Kömpf [Allemagne] ; Roland Wenzelburger [Allemagne] ; Günther Deuschl [Allemagne] ; Wolfgang Heide [Allemagne] ; Christoph Helmchen [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2006-03.

RBID : ISTEX:95DDEB206C0E1E218A379AAA934DC9E6BFA88457

Descripteurs français

Pascal (Inist)
- Cervelet, Cinématique, Coordination, Main, Oeil, Système nerveux pathologie, Tremblement.

English descriptors

KwdEn :
- Adult, Age of Onset, Aged, Aged, 80 and over, Biomechanical Phenomena, Cerebellum, Cerebellum (physiopathology), Coordination, Essential Tremor (epidemiology), Essential Tremor (physiopathology), Eye, Fixation, Ocular (physiology), Hand, Hand (physiology), Humans, Kinematics, Middle Aged, Nervous system diseases, Psychomotor Performance (physiology), Saccades (physiology), Time Factors, Tremor, cerebellum, essential tremor, eye–hand coordination, kinematics, saccade.
MESH :
- epidemiology : Essential Tremor.
- physiology : Fixation, Ocular, Hand, Psychomotor Performance, Saccades.
- physiopathology : Cerebellum, Essential Tremor.
- Adult, Age of Onset, Aged, Aged, 80 and over, Biomechanical Phenomena, Humans, Middle Aged, Time Factors.

Abstract

Patients with essential tremor (ET) or with cerebellar lesions have in common oculomotor abnormalities, with the exception of saccadic eye movements, which do not seem to be involved in ET. Since grasping is prolonged in ET and might be related to saccadic dysmetria, we tested whether simultaneous hand pointing could unmask it. Twelve ET patients and 14 controls performed saccades with and without simultaneous pointing movements to the same targets, and with and without a gap between the disappearance of the fixation point and the appearance of the target. Eye movements were recorded with the magnetic search‐coil method, hand movements with an ultrasound‐emitting probe. ET patients did not have saccadic dysmetria, and contrary to normal subjects their saccadic latency did not decrease during combined eye–hand movements compared with saccades performed in isolation. Hand movements had a longer duration in ET patients, with decreased peak acceleration, an increased latency of the peak velocity, and peak deceleration. In conclusion, this first study on eye–hand coordination in ET revealed abnormal kinematic changes in the early phase of pointing movements. These changes might be related to cerebellar disease but they are independent of the intention tremor component and saccade performance. © 2005 Movement Disorder Society

Url:

https://api.istex.fr/document/95DDEB206C0E1E218A379AAA934DC9E6BFA88457/fulltext/pdf

DOI: 10.1002/mds.20729

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ISTEX:95DDEB206C0E1E218A379AAA934DC9E6BFA88457

Le document en format XML

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<term>Cerebellum</term>
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<front><div type="abstract" xml:lang="en">Patients with essential tremor (ET) or with cerebellar lesions have in common oculomotor abnormalities, with the exception of saccadic eye movements, which do not seem to be involved in ET. Since grasping is prolonged in ET and might be related to saccadic dysmetria, we tested whether simultaneous hand pointing could unmask it. Twelve ET patients and 14 controls performed saccades with and without simultaneous pointing movements to the same targets, and with and without a gap between the disappearance of the fixation point and the appearance of the target. Eye movements were recorded with the magnetic search‐coil method, hand movements with an ultrasound‐emitting probe. ET patients did not have saccadic dysmetria, and contrary to normal subjects their saccadic latency did not decrease during combined eye–hand movements compared with saccades performed in isolation. Hand movements had a longer duration in ET patients, with decreased peak acceleration, an increased latency of the peak velocity, and peak deceleration. In conclusion, this first study on eye–hand coordination in ET revealed abnormal kinematic changes in the early phase of pointing movements. These changes might be related to cerebellar disease but they are independent of the intention tremor component and saccade performance. © 2005 Movement Disorder Society</div>
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<front><div type="abstract" xml:lang="en">Patients with essential tremor (ET) or with cerebellar lesions have in common oculomotor abnormalities, with the exception of saccadic eye movements, which do not seem to be involved in ET. Since grasping is prolonged in ET and might be related to saccadic dysmetria, we tested whether simultaneous hand pointing could unmask it. Twelve ET patients and 14 controls performed saccades with and without simultaneous pointing movements to the same targets, and with and without a gap between the disappearance of the fixation point and the appearance of the target. Eye movements were recorded with the magnetic search-coil method, hand movements with an ultrasound-emitting probe. ET patients did not have saccadic dysmetria, and contrary to normal subjects their saccadic latency did not decrease during combined eye-hand movements compared with saccades performed in isolation. Hand movements had a longer duration in ET patients, with decreased peak acceleration, an increased latency of the peak velocity, and peak deceleration. In conclusion, this first study on eye-hand coordination in ET revealed abnormal kinematic changes in the early phase of pointing movements. These changes might be related to cerebellar disease but they are independent of the intention tremor component and saccade performance.</div>
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<front><div type="abstract" xml:lang="en">Patients with essential tremor (ET) or with cerebellar lesions have in common oculomotor abnormalities, with the exception of saccadic eye movements, which do not seem to be involved in ET. Since grasping is prolonged in ET and might be related to saccadic dysmetria, we tested whether simultaneous hand pointing could unmask it. Twelve ET patients and 14 controls performed saccades with and without simultaneous pointing movements to the same targets, and with and without a gap between the disappearance of the fixation point and the appearance of the target. Eye movements were recorded with the magnetic search‐coil method, hand movements with an ultrasound‐emitting probe. ET patients did not have saccadic dysmetria, and contrary to normal subjects their saccadic latency did not decrease during combined eye–hand movements compared with saccades performed in isolation. Hand movements had a longer duration in ET patients, with decreased peak acceleration, an increased latency of the peak velocity, and peak deceleration. In conclusion, this first study on eye–hand coordination in ET revealed abnormal kinematic changes in the early phase of pointing movements. These changes might be related to cerebellar disease but they are independent of the intention tremor component and saccade performance. © 2005 Movement Disorder Society</div>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Eye–hand coordination in essential tremor

Eye–hand coordination in essential tremor

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