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- Title
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations.
- Authors
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
A 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.
- Subjects
RHODOPSIN; RETINAL rod photoreceptor cells; GENETIC mutation; PROTEIN expression; PHENOTYPES; RETINAL degeneration
- Publication
Scientific Reports, 2020, Vol 10, Issue 1, p1
- ISSN
2045-2322
- Publication type
Article
- DOI
10.1038/s41598-020-69456-3