An Optical Coherence Tomography-Based Measure as an Independent Estimate of Retinal Function in Retinitis Pigmentosa

Author:

Paez-Escamilla Manuel12,Alabek Michelle L.1,Beale Oliver1,Prensky Colin J.1,Lejoyeux Raphael134,Friberg Thomas R.1,Sahel Jose-Alain1,Rosin Boris1

Affiliation:

1. Department of Ophthalmology/UPMC Vision Institute, University of Pittsburgh Medical Center (UPMC), 1622 Locust Street, Pittsburgh, PA 15219, USA

2. Department of Ophthalmology, McGill University Health Centre, Montreal, QC H4A 3J1, Canada

3. Rothschild Foundation Hospital, 75019 Paris, France

4. Institut Oeil Paupiere, Viry-Chatillon, 91170 Paris, France

Abstract

Background: With the clinical advances in the field of gene therapy, the development of objective measures of visual function of patients with inherited retinal dystrophies (IRDs) is of utmost importance. Here, we propose one such measure. Methods: We retrospectively analyzed data from a cohort of 194 eyes of 97 genetically diagnosed patients with retinitis pigmentosa (RP), the most common IRD, followed at the UPMC Vision Institute. The analyzed data included the reflectivity ratio (RR) of the retinal nerve fiber layer (RNFL) to that of the entire retina, visual acuity (VA) and the thickness of the retinal outer nuclear layer (ONL) and the RNFL. Results: There was a strong positive correlation between the RR and VA. Both VA and the RR were negatively correlated with disease duration; VA, but not the RR, was negatively correlated with age. The RR correlated with the ONL but not with the RNFL thickness or the intraocular pressure. Age, RR, disease duration and ONL thickness were found to be independent predictors of VA by multivariate analysis. Conclusion: The OCT RR could serve as an independent predictor of visual acuity, and by extension of retinal function, in genetically diagnosed RP patients. Such objective measures can be of great value in patient selection for therapeutic trials.

Funder

Foundation Fighting Blindness

Research to Prevent Blindness’ Unrestricted and NIH CORE Grant

Publisher

MDPI AG

Subject

Clinical Biochemistry

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