3.9 Article

A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy

Journal

CLINICAL OPHTHALMOLOGY
Volume 15, Issue -, Pages 939-952

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OPTH.S292527

Keywords

virtual reality; mobility; orientation; gene therapy; LCA; RPE65

Categories

Funding

  1. Hope for Vision
  2. Pennsylvania Lions Sight Conservation and Research Foundation
  3. F.M. Kirby Foundation
  4. Center for Advanced Retinal and Ocular Therapeutics (CAROT), University of Pennsylvania

Ask authors/readers for more resources

This study demonstrates the potential of using a virtual reality orientation and mobility test to assess the impact of visual dysfunction and improvement following treatments in patients with inherited retinal degenerations. The VR-O&M system proved useful, particularly in challenging scenarios such as pediatric patients with severe IRDs.
Purpose: To test the ability of a virtual reality (VR) orientation and mobility (O&M) protocol to serve a measure of functional vision for patients with inherited retinal degenerations (IRDs). Methods: A VR-O&M protocol designed using a commercially available VR hardware was tested in normally sighted control subjects (n=7; ages 10-35yo; Average 22.5yo) and patients with RPE65-associated Leber Congenital Amaurosis (n=3; ages 7-18yo; Average 12.7yo), in two of them before and after gene therapy. Patients underwent perimetry and full-field sensitivity testing. VR-O&M parameters correlated with the visual dysfunction. Results: Visual acuities in RPE65 patients were on average worse than 20/200, dark-adapted sensitivity losses >5 log units, and fields constricted between 20 degrees and 40 degrees. Before treatment, patients required similar to 1000-fold brighter environment to navigate, had at least x4 more collisions, and were slower both to orient and navigate compared to control subjects. Improvements in cone- (by 1-2 L.u.) and rod-mediated (by >4 L.u.) sensitivities post-treatment led to fewer collisions (at least by half) at similar to 100-fold dimmer luminances, and to x4 times faster navigation times. Conclusion: This study provides proof-of-concept data in support for the use of VR-O&M systems to quantify the impact that the visual dysfunction and improvement of vision following treatments has on functional vision in IRDs. The VR-O&M was useful in potentially challenging scenarios such as in pediatric patients with severe IRDs. Translational Relevance: A VR-O&M test will provide much needed flexibility, both in its deployment as well as in the possibility to test various attributes of vision that may be impacted by gene therapy in the setting of translational studies. Precis: This study provides proof-of-concept data in support for the use of a virtual reality orientation and mobility test to quantify the impact of the disease and of treatments thereof on functional vision in inherited retinal degenerations.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.9
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available