Introduction: While most head movements in daily life are active, most tools used to assess vestibular deficits rely on passive head movements. A single gain value is not sufficient to quantify gaze stabilization efficiency during active movements in vestibular deficit patients. Moreover, during active gaze shifts, anticipatory mechanisms come into play. Our aim was to explore the extent to which previously described compensatory mechanisms are employed in patients with bilateral vestibular loss.
Methods: We used a Video Head Impulse Test (vHIT) to simultaneously record eye and head movements during a video Active Gaze Shift Test (vAGST). Thirty-eight patients with bilateral vestibular deficits and 61 control subjects were tested.
Results: Despite impaired performance on caloric tests and vHIT, most patients exhibited normal gaze stabilization (gain = 0.92 ± 0.1) during active gaze shifts up to a head speed ('stall speed') of approximately 140 ± 60°/sec, compared to 280 ± 65°/sec in controls. Our results indicate that BVD patients spontaneously adopt a head speed during active horizontal movements that significantly improves gaze stabilization compared to passive movements. The stall speed correlates with the spontaneous head speed typically adopted by BVD patients and controls in daily activities. As a consequence of the reduction in head speed and corrective saccades, patients also showed an increased delay in gaze stabilization (413 ± 105 ms in BVD patients versus 358 ± 82 ms in controls) at the end of the gaze shift, which might become disabling for certain tasks.
Discussion: Recent model suggests that compensatory eye movements, which stabilize gaze during the counter rotation phase of active gaze shifts, are predictive in nature. vAGST is not designed to provide an etiological diagnosis but rather a functional assessment of the patient's ability to generate predictive eye movements that compensate for vestibular sensor deficits. Understanding the quality of the patient's sensory predictions can also shed light on vestibular symptoms, even in cases where no vestibular sensor deficit is detected. This suggest that quality of life and oscillopsia questionnaires should distinguish between predictable and unpredictable movements.
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http://dx.doi.org/10.3389/fneur.2024.1509762 | DOI Listing |
BMJ Open
December 2024
Faculty of Medicine and Health Sciences, Department of Rehabilitation Sciences, Ghent University, Gent, Belgium.
Introduction: A vestibular deficit can have a substantial impact on the overall development of children. Therefore, it is of utmost importance that vestibular-impaired problems are treated early and effectively through Vestibular Rehabilitation Therapy (VRT). Although VRT is sufficiently proven and standardised in adults, there remains a lack of research examining its efficacy in children.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, USA.
The vestibular system is vital for maintaining stable vision during daily activities. When peripheral vestibular input is lost, patients initially experience impaired gaze stability due to reduced effectiveness of the vestibular-ocular-reflex pathway. To aid rehabilitation, patients are often prescribed gaze-stabilization exercises during which they make self-initiated active head movements.
View Article and Find Full Text PDFDeveloping populations of connected neurons often share spatial and/or temporal features that anticipate their assembly. A unifying spatiotemporal motif might link sensory, central, and motor populations that comprise an entire circuit. In the sensorimotor reflex circuit that stabilizes vertebrate gaze, central and motor partners are paired in time (birthdate) and space (dorso-ventral).
View Article and Find Full Text PDFGraefes Arch Clin Exp Ophthalmol
January 2025
Frankfurt Institute for Advanced Studies (FIAS), Frankfurt am Main, Germany.
Purpose: Our study presents a virtual reality-based tangent screen test (VTS) to measure subjective ocular deviations including torsion in nine directions of gaze. The test was compared to the analogous Harms tangent screen test (HTS).
Methods: We used an Oculus Go controller and head-mounted-display with rotation sensors to measure patient's head orientation for the VTS.
Science
January 2025
Department of Otolaryngology, Department of Neuroscience and Physiology, and the Neuroscience Institute, NYU Grossman School of Medicine, New York, NY, USA.
Vertebrates stabilize gaze using a neural circuit that transforms sensed instability into compensatory counterrotation of the eyes. Sensory feedback tunes this vestibulo-ocular reflex throughout life. We studied the functional development of vestibulo-ocular reflex circuit components in the larval zebrafish, with and without sensation.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!