Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations

Author:

Cideciyan Artur V.,Jacobson Samuel G.,Roman Alejandro J.,Sumaroka Alexander,Wu Vivian,Charng Jason,Lisi Brianna,Swider Malgorzata,Aguirre Gustavo D.,Beltran William A.

Abstract

AbstractA common inherited retinal disease is caused by mutations in RHO expressed in rod photoreceptors that provide vision in dim ambient light. Approximately half of all RHO mutations result in a Class B phenotype where mutant rods are retained in some retinal regions but show severe degeneration in other regions. We determined the natural history of dysfunction and degeneration of retained rods by serially evaluating patients. Even when followed for more than 20 years, rod function and structure at some retinal locations could remain unchanged. Other locations showed loss of both vision and photoreceptors but the rate of rod vision loss was greater than the rate of photoreceptor degeneration. This unexpected divergence in rates with disease progression implied the development of a rod function deficit beyond loss of cells. The divergence of progression rates was also detectable over a short interval of 2 years near the health-disease transition in the superior retina. A model of structure–function relationship supported the existence of a large rod function deficit which was also most prominent near regions of health-disease transition. Our studies support the realistic therapeutic goal of improved night vision for retinal regions specifically preselected for rod function deficit in patients.

Funder

IvericBio

National Eye Institute

Ionis Pharmaceuticals

Research to Prevent Blindness

Foundation Fighting Blindness

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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