A loss of a velocity‐duration trade‐off impairs movement precision in patients with cerebellar degeneration
Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inab...
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Published in | The European journal of neuroscience Vol. 48; no. 4; pp. 1976 - 1989 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
France
Wiley Subscription Services, Inc
01.08.2018
John Wiley and Sons Inc |
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Online Access | Get full text |
ISSN | 0953-816X 1460-9568 1460-9568 |
DOI | 10.1111/ejn.14062 |
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Abstract | Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inability to correct them; however, it should not boost “motor noise.” However, dysmetria, a loss of endpoint precision and an increase in endpoint variability (“motor noise”) of goal‐directed movements is the central aspect of cerebellar ataxia. Does the prevention of dysmetria or “motor noise” by the healthy cerebellum tell us anything about its normal function? We hypothesize that the healthy cerebellum is able to prevent dysmetria by adjusting movement duration such as to compensate changes in movement velocity. To address this question, we studied fast goal‐directed index finger movements in patients with global cerebellar degeneration and in healthy subjects. We demonstrate that healthy subjects are able to maintain endpoint precision despite continuous fluctuations in movement velocity because they are able to adjust the overall movement duration in a fully compensatory manner (“velocity‐duration trade‐off”). We furthermore provide evidence that this velocity‐duration trade‐off accommodated by the healthy cerebellum is based on a priori information on the future movement velocity. This ability is lost in cerebellar disease. We suggest that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum‐based velocity‐duration trade‐off mechanism that continuously fine‐tunes movement durations using information on the expected velocity of the upcoming movement.
We show that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum‐based velocity‐duration trade‐off mechanism that continuously fine‐tunes movement durations using information on the expected velocity of the upcoming movement. |
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AbstractList | Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inability to correct them; however, it should not boost “motor noise.” However, dysmetria, a loss of endpoint precision and an increase in endpoint variability (“motor noise”) of goal‐directed movements is the central aspect of cerebellar ataxia. Does the prevention of dysmetria or “motor noise” by the healthy cerebellum tell us anything about its normal function? We hypothesize that the healthy cerebellum is able to prevent dysmetria by adjusting movement duration such as to compensate changes in movement velocity. To address this question, we studied fast goal‐directed index finger movements in patients with global cerebellar degeneration and in healthy subjects. We demonstrate that healthy subjects are able to maintain endpoint precision despite continuous fluctuations in movement velocity because they are able to adjust the overall movement duration in a fully compensatory manner (“velocity‐duration trade‐off”). We furthermore provide evidence that this velocity‐duration trade‐off accommodated by the healthy cerebellum is based on a priori information on the future movement velocity. This ability is lost in cerebellar disease. We suggest that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum‐based velocity‐duration trade‐off mechanism that continuously fine‐tunes movement durations using information on the expected velocity of the upcoming movement.
We show that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum‐based velocity‐duration trade‐off mechanism that continuously fine‐tunes movement durations using information on the expected velocity of the upcoming movement. Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inability to correct them; however, it should not boost "motor noise." However, dysmetria, a loss of endpoint precision and an increase in endpoint variability ("motor noise") of goal-directed movements is the central aspect of cerebellar ataxia. Does the prevention of dysmetria or "motor noise" by the healthy cerebellum tell us anything about its normal function? We hypothesize that the healthy cerebellum is able to prevent dysmetria by adjusting movement duration such as to compensate changes in movement velocity. To address this question, we studied fast goal-directed index finger movements in patients with global cerebellar degeneration and in healthy subjects. We demonstrate that healthy subjects are able to maintain endpoint precision despite continuous fluctuations in movement velocity because they are able to adjust the overall movement duration in a fully compensatory manner ("velocity-duration trade-off"). We furthermore provide evidence that this velocity-duration trade-off accommodated by the healthy cerebellum is based on a priori information on the future movement velocity. This ability is lost in cerebellar disease. We suggest that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum-based velocity-duration trade-off mechanism that continuously fine-tunes movement durations using information on the expected velocity of the upcoming movement.Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inability to correct them; however, it should not boost "motor noise." However, dysmetria, a loss of endpoint precision and an increase in endpoint variability ("motor noise") of goal-directed movements is the central aspect of cerebellar ataxia. Does the prevention of dysmetria or "motor noise" by the healthy cerebellum tell us anything about its normal function? We hypothesize that the healthy cerebellum is able to prevent dysmetria by adjusting movement duration such as to compensate changes in movement velocity. To address this question, we studied fast goal-directed index finger movements in patients with global cerebellar degeneration and in healthy subjects. We demonstrate that healthy subjects are able to maintain endpoint precision despite continuous fluctuations in movement velocity because they are able to adjust the overall movement duration in a fully compensatory manner ("velocity-duration trade-off"). We furthermore provide evidence that this velocity-duration trade-off accommodated by the healthy cerebellum is based on a priori information on the future movement velocity. This ability is lost in cerebellar disease. We suggest that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum-based velocity-duration trade-off mechanism that continuously fine-tunes movement durations using information on the expected velocity of the upcoming movement. Current theories discussing the role of the cerebellum have been consistently pointing towards the concept of motor learning. The unavailability of a structure for motor learning able to use information on past errors to change future movements should cause consistent metrical deviations and an inability to correct them; however, it should not boost “motor noise.” However, dysmetria, a loss of endpoint precision and an increase in endpoint variability (“motor noise”) of goal‐directed movements is the central aspect of cerebellar ataxia. Does the prevention of dysmetria or “motor noise” by the healthy cerebellum tell us anything about its normal function? We hypothesize that the healthy cerebellum is able to prevent dysmetria by adjusting movement duration such as to compensate changes in movement velocity. To address this question, we studied fast goal‐directed index finger movements in patients with global cerebellar degeneration and in healthy subjects. We demonstrate that healthy subjects are able to maintain endpoint precision despite continuous fluctuations in movement velocity because they are able to adjust the overall movement duration in a fully compensatory manner (“velocity‐duration trade‐off”). We furthermore provide evidence that this velocity‐duration trade‐off accommodated by the healthy cerebellum is based on a priori information on the future movement velocity. This ability is lost in cerebellar disease. We suggest that the dysmetria observed in cerebellar patients is a direct consequence of the loss of a cerebellum‐based velocity‐duration trade‐off mechanism that continuously fine‐tunes movement durations using information on the expected velocity of the upcoming movement. |
Author | Markanday, Akshay Messner, Julian Thier, Peter |
AuthorAffiliation | 1 Hertie Institute for Clinical Brain Research Tübingen Germany 2 Werner Reichardt Centre for Integrative Neuroscience (CIN) Tübingen Germany |
AuthorAffiliation_xml | – name: 2 Werner Reichardt Centre for Integrative Neuroscience (CIN) Tübingen Germany – name: 1 Hertie Institute for Clinical Brain Research Tübingen Germany |
Author_xml | – sequence: 1 givenname: Akshay surname: Markanday fullname: Markanday, Akshay organization: Hertie Institute for Clinical Brain Research – sequence: 2 givenname: Julian surname: Messner fullname: Messner, Julian organization: Hertie Institute for Clinical Brain Research – sequence: 3 givenname: Peter orcidid: 0000-0001-5909-4222 surname: Thier fullname: Thier, Peter email: thier@uni-tuebingen.de organization: Werner Reichardt Centre for Integrative Neuroscience (CIN) |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29972715$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12311_022_01438_9 crossref_primary_10_1038_s41467_023_37981_0 crossref_primary_10_1371_journal_pcbi_1011322 crossref_primary_10_1146_annurev_vision_091718_015000 crossref_primary_10_1111_ene_14312 |
Cites_doi | 10.1152/jn.00007.2011 10.1093/brain/awu115 10.1007/s002210000417 10.1016/0042-6989(87)90071-X 10.1021/ac60214a047 10.1016/0025-5564(71)90051-4 10.1007/s002210050365 10.1523/JNEUROSCI.6353-11.2012 10.1038/35011062 10.1111/j.1460-9568.2007.05996.x 10.1146/annurev.ne.05.030182.001423 10.1146/annurev-neuro-060909-153135 10.1073/pnas.0706032105 10.1016/j.conb.2015.03.013 10.1523/JNEUROSCI.3901-10.2010 10.1016/0014-4886(75)90225-3 10.3109/01658109609009677 10.1136/jnnp.38.12.1163 10.1212/01.wnl.0000219042.60538.92 10.1016/0006-8993(95)01514-0 10.1113/jphysiol.1969.sp008820 |
ContentType | Journal Article |
Copyright | 2018 The Authors. published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. 2018 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. Copyright © 2018 Federation of European Neuroscience Societies and John Wiley & Sons Ltd |
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Keywords | cerebellar ataxia duration adjustment precision motor noise |
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StartPage | 1976 |
SubjectTerms | Adult Aged Biomechanical Phenomena - physiology Cerebellar ataxia Cerebellar Ataxia - physiopathology Cerebellum Clinical and Translational Neuroscience Concept learning Degeneration duration adjustment Female Fingers - physiology Humans Male Middle Aged Motor Activity - physiology motor noise Motor skill learning Noise precision Psychomotor Performance - physiology Research Report Time Factors Velocity |
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Title | A loss of a velocity‐duration trade‐off impairs movement precision in patients with cerebellar degeneration |
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