Literature DB >> 36069428

Compensatory saccades differ between those with vestibular hypofunction and multiple sclerosis pointing to unique roles for peripheral and central vestibular inputs.

Andrew R Wagner1,2, Colin R Grove3, Brian J Loyd4, Leland E Dibble5, Michael C Schubert3,6.   

Abstract

Individuals with peripheral or central vestibular dysfunction recruit compensatory saccades (CSs) in response to high acceleration, yaw head impulses. Although CSs have been shown to be an effective strategy for reducing gaze position error (GPE) in individuals with peripheral hypofunction, for individuals with central vestibular dysfunction, the effectiveness of CS is unknown. The purpose of our study was to compare the effectiveness of CS, defined as the ability to compensate for head velocity and eye position errors, between persons with central and peripheral vestibular dysfunction. We compared oculomotor responses during video head impulse testing between individuals with unilateral peripheral vestibular deafferentation, a disorder of the peripheral vestibular afferents, and individuals with multiple sclerosis, a condition affecting the central vestibular pathways. We hypothesized that relative to individuals with peripheral lesions, individuals with central dysfunction would recruit CSs that were delayed and inappropriately scaled to head velocity and GPE. We show that CSs recruited by persons with central vestibular pathology were not uniformly deficient but instead were of a sufficient velocity to compensate for reductions in VOR gain. Compared to those with peripheral vestibular lesions, individuals with central pathology also recruited earlier covert CS with amplitudes that were better corrected for GPE. Conversely, those with central lesions showed greater variability in the amplitude of overt CS relative to GPE. These data point to a unique role for peripheral and central vestibular inputs in the recruitment of CS and suggest that covert CSs are an effective oculomotor strategy for individuals with multiple sclerosis.NEW & NOTEWORTHY Compensatory saccades (CSs) are recruited by individuals with unilateral vestibular deafferentation (UVD) to compensate for an impaired vestibulo-ocular reflex (VOR). The effectiveness of CS in multiple sclerosis (MS), a central vestibular impairment, is unknown. We show that in UVD and in MS, covert CSs compensate for reduced VOR gain and minimize gaze position error (GPE), yet in >50% of individuals with MS, overt CS worsened GPE, suggesting unique roles for peripheral and central vestibular inputs.

Entities:  

Keywords:  compensatory saccade; multiple sclerosis; vHIT; vestibular hypofunction; vestibulo-ocular reflex

Mesh:

Year:  2022        PMID: 36069428      PMCID: PMC9550564          DOI: 10.1152/jn.00220.2022

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.974


  26 in total

1.  Vestibulo-ocular reflex involvement in childhood-onset multiple sclerosis.

Authors:  Gorkem Ertugrul; Bahadır Konuskan; Ismail Solmaz; Banu Anlar; Songul Aksoy
Journal:  Mult Scler Relat Disord       Date:  2020-06-22       Impact factor: 4.339

2.  Video head impulse test can detect brainstem dysfunction in multiple sclerosis.

Authors:  Ivan Pavlović; Berislav Ruška; Tin Pavičić; Magdalena Krbot Skorić; Luka Crnošija; Ivan Adamec; Mario Habek
Journal:  Mult Scler Relat Disord       Date:  2017-04-07       Impact factor: 4.339

3.  New insights into vestibular-saccade interaction based on covert corrective saccades in patients with unilateral vestibular deficits.

Authors:  Paolo Colagiorgio; Maurizio Versino; Silvia Colnaghi; Silvia Quaglieri; Marco Manfrin; Ewa Zamaro; Georgios Mantokoudis; David S Zee; Stefano Ramat
Journal:  J Neurophysiol       Date:  2017-04-12       Impact factor: 2.714

4.  Impact of artifacts on VOR gain measures by video-oculography in the acute vestibular syndrome.

Authors:  Georgios Mantokoudis; Ali S Saber Tehrani; Amy Wozniak; Karin Eibenberger; Jorge C Kattah; Cynthia I Guede; David S Zee; David E Newman-Toker
Journal:  J Vestib Res       Date:  2016-11-03       Impact factor: 2.435

5.  Vestibular evoked myogenic potentials and MRI in early multiple sclerosis: Validation of the VEMP score.

Authors:  Luka Crnošija; Magdalena Krbot Skorić; Tereza Gabelić; Ivan Adamec; Mario Habek
Journal:  J Neurol Sci       Date:  2016-11-14       Impact factor: 3.181

6.  VOR gain by head impulse video-oculography differentiates acute vestibular neuritis from stroke.

Authors:  Georgios Mantokoudis; Ali S Saber Tehrani; Amy Wozniak; Karin Eibenberger; Jorge C Kattah; Cynthia I Guede; David S Zee; David E Newman-Toker
Journal:  Otol Neurotol       Date:  2015-03       Impact factor: 2.311

7.  Gaze Stability, Dynamic Balance and Participation Deficits in People with Multiple Sclerosis at Fall-Risk.

Authors:  Hina Garg; Leland E Dibble; Michael C Schubert; Jim Sibthorp; K Bo Foreman; Eduard Gappmaier
Journal:  Anat Rec (Hoboken)       Date:  2018-08-05       Impact factor: 2.064

8.  Mechanism of dynamic visual acuity recovery with vestibular rehabilitation.

Authors:  Michael C Schubert; Americo A Migliaccio; Richard A Clendaniel; Amir Allak; John P Carey
Journal:  Arch Phys Med Rehabil       Date:  2008-03       Impact factor: 3.966

9.  Early adaptation and compensation of clinical vestibular responses after unilateral vestibular deafferentation surgery.

Authors:  Georgios Mantokoudis; Michael C Schubert; Ali S Saber Tehrani; Aaron L Wong; Yuri Agrawal
Journal:  Otol Neurotol       Date:  2014-01       Impact factor: 2.311

10.  Improvement After Vestibular Rehabilitation Not Explained by Improved Passive VOR Gain.

Authors:  Jennifer L Millar; Yoav Gimmon; Dale Roberts; Michael C Schubert
Journal:  Front Neurol       Date:  2020-02-20       Impact factor: 4.003

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