Evidence map›Paper›PMID 36103550›Full record

ArticlePLoS biology2022

A prosthesis utilizing natural vestibular encoding strategies improves sensorimotor performance in monkeys.

Kantapon Pum Wiboonsaksakul, Dale C Roberts, Charles C Della Santina, Kathleen E Cullen

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2022. 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
1.0field-weighted citation impact, top 24% 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, 12 citations in OpenAlex.

  1. Acceleration and Velocity Dissociate Temporal Phases of Postural Control in Rhesus Macaques.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Vestibular prosthesis: from basic research to clinics.Frontiers in integrative neuroscience · 2023
    Review
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

4 authors at 1 institution in 1 country.

Kantapon Pum WiboonsaksakulDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine; Baltimore, Maryland, United States of America.ORCID 0000-0002-5468-9718
Dale C RobertsDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine; Baltimore, Maryland, United States of America.
Charles C Della SantinaDepartment of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine; Baltimore, Maryland, United States of America.
Kathleen E CullenDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine; Baltimore, Maryland, United States of America.
Johns Hopkins University · US

Funding

The Physiology of Vestibular CompensationR01DC002390 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI Kathleen E Cullen · 1995 to 2026
$10.7M
Neural Computations Underlying Cancellation of the Vestibular Consequences of Voluntary MovementR01DC018061 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI Kathleen E Cullen · 2019 to 2026
$4.0M
NIDCD NIH HHS R01 DC002390NIDCD NIH HHS R01 DC018061
6 · The paper itself

Abstract

Sensory pathways provide complex and multifaceted information to the brain. Recent advances have created new opportunities for applying our understanding of the brain to sensory prothesis development. Yet complex sensor physiology, limited numbers of electrodes, and nonspecific stimulation have proven to be a challenge for many sensory systems. In contrast, the vestibular system is uniquely suited for prosthesis development. Its peripheral anatomy allows site-specific stimulation of 3 separate sensory organs that encode distinct directions of head motion. Accordingly, here, we investigated whether implementing natural encoding strategies improves vestibular prosthesis performance. The eye movements produced by the vestibulo-ocular reflex (VOR), which plays an essential role in maintaining visual stability, were measured to quantify performance. Overall, implementing the natural tuning dynamics of vestibular afferents produced more temporally accurate VOR eye movements. Exploration of the parameter space further revealed that more dynamic tunings were not beneficial due to saturation and unnatural phase advances. Trends were comparable for stimulation encoding virtual versus physical head rotations, with gains enhanced in the latter case. Finally, using computational methods, we found that the same simple model explained the eye movements evoked by sinusoidal and transient stimulation and that a stimulation efficacy substantially less than 100% could account for our results. Taken together, our results establish that prosthesis encodings that incorporate naturalistic afferent dynamics and account for activation efficacy are well suited for restoration of gaze stability. More generally, these results emphasize the benefits of leveraging the brain's endogenous coding strategies in prosthesis development to improve functional outcomes.

Indexed as

Artificial LimbsVestibule, LabyrinthAnimalsEye MovementsMacaca mulattaReflex, Vestibulo-Ocular

Identifiers

PMID36103550
PMCPMC9473632
OpenAlexW4295786969

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.