Evidence map›Paper›PMID 27571363›Full record

ArticlePloS one2016

Impaired Spatio-Temporal Predictive Motor Timing Associated with Spinocerebellar Ataxia Type 6.

Robin Broersen, Yoshiyuki Onuki, Abdel R Abdelgabar, Cullen B Owens, Samuel Picard, Jessica Willems, Henk-Jan Boele, Valeria Gazzola, Ysbrand D Van der Werf, Chris I De Zeeuw

Open access · goldAbstract readControlled Clinical Trial
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  8. Cerebellar Role in Predictive Control of Eye Velocity Initiation and Termination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Robin BroersenNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-2555-9719
Yoshiyuki OnukiNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Abdel R AbdelgabarNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Cullen B OwensDepartment of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Samuel PicardNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Jessica WillemsDepartment of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Henk-Jan BoeleDepartment of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Valeria GazzolaNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Ysbrand D Van der WerfNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Chris I De ZeeuwNetherlands Institute for Neuroscience, Royal Dutch Academy of Arts & Sciences, Amsterdam, The Netherlands.
Netherlands Institute for Neuroscience · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many daily life activities demand precise integration of spatial and temporal information of sensory inputs followed by appropriate motor actions. This type of integration is carried out in part by the cerebellum, which has been postulated to play a central role in learning and timing of movements. Cerebellar damage due to atrophy or lesions may compromise forward-model processing, in which both spatial and temporal cues are used to achieve prediction for future motor states. In the present study we sought to further investigate the cerebellar contribution to predictive and reactive motor timing, as well as to learning of sequential order and temporal intervals in these tasks. We tested patients with spinocerebellar ataxia type 6 (SCA6) and healthy controls for two related motor tasks; one requiring spatio-temporal prediction of dynamic visual stimuli and another one requiring reactive timing only. We found that healthy controls established spatio-temporal prediction in their responses with high temporal precision, which was absent in the cerebellar patients. SCA6 patients showed lower predictive motor timing, coinciding with a reduced number of correct responses during the 'anticipatory' period on the task. Moreover, on the task utilizing reactive motor timing functions, control participants showed both sequence order and temporal interval learning, whereas patients only showed sequence order learning. These results suggest that SCA6 affects predictive motor timing and temporal interval learning. Our results support and highlight cerebellar contribution to timing and argue for cerebellar engagement during spatio-temporal prediction of upcoming events.

Indexed as

AgedAged, 80 and overCerebellumFemaleHumansLearningMaleMiddle AgedPhotic StimulationPsychomotor PerformanceSpinocerebellar AtaxiasTime Perception

Identifiers

PMID27571363
PMCPMC5003364
OpenAlexW2507937021

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.