Evidence map›Paper›PMID 31959778›Full record

ArticleScientific reports2020

Head motion predictability explains activity-dependent suppression of vestibular balance control.

H Dietrich, F Heidger, R Schniepp, P R MacNeilage, S Glasauer, M Wuehr

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

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  4. Roles for cerebellum and subsumption architecture in central pattern generation.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2024
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  9. The Neural Basis for Biased Behavioral Responses Evoked by Galvanic Vestibular Stimulation in Primates.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  10. Article
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  15. Review
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  17. Inflight head stabilization associated with wingbeat cycle and sonar emissions in the lingual echolocating Egyptian fruit bat, Rousettus aegyptiacus.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2021
    Article
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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

6 authors at 4 institutions in 2 countries.

H Dietrich *German Center for Vertigo and Balance Disorders, University Hospital, LMU, Munich, Germany.
F Heidger *Department of Neurology, University Hospital, LMU, Munich, Germany.
R SchnieppGerman Center for Vertigo and Balance Disorders, University Hospital, LMU, Munich, Germany.
P R MacNeilageGerman Center for Vertigo and Balance Disorders, University Hospital, LMU, Munich, Germany.
S GlasauerGerman Center for Vertigo and Balance Disorders, University Hospital, LMU, Munich, Germany.
M WuehrGerman Center for Vertigo and Balance Disorders, University Hospital, LMU, Munich, Germany. Max.Wuehr@med.uni-muenchen.de.
German Center for Lung Research · DELudwig-Maximilians-Universität München · DEBrandenburg University of Technology Cottbus-Senftenberg · DELMU Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vestibular balance control is dynamically weighted during locomotion. This might result from a selective suppression of vestibular inputs in favor of a feed-forward balance regulation based on locomotor efference copies. The feasibility of such a feed-forward mechanism should however critically depend on the predictability of head movements (HMP) during locomotion. To test this, we studied in 10 healthy subjects the differential impact of a stochastic vestibular stimulation (SVS) on body sway (center-of-pressure, COP) during standing and walking at different speeds and compared it to activity-dependent changes in HMP. SVS-COP coupling was determined by correlation analysis in frequency and time domains. HMP was quantified as the proportion of head motion variance that can be explained by the average head trajectory across the locomotor cycle. SVS-COP coupling decreased from standing to walking and further dropped with faster locomotion. Correspondingly, HMP increased with faster locomotion. Furthermore, SVS-COP coupling depended on the gait-cycle-phase with peaks corresponding to periods of least HMP. These findings support the assumption that during stereotyped human self-motion, locomotor efference copies selectively replace vestibular cues, similar to what was previously observed in animal models.

Indexed as

AdultAnimalsCuesElectric StimulationFemaleGaitHeadHead MovementsHumansLocomotionMalePostural BalanceStanding PositionVestibule, LabyrinthWalking

Identifiers

PMID31959778
PMCPMC6971007
OpenAlexW3002663572

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.