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Extending the Spectrum of EYS-Associated Retinal Disease to Macular Dystrophy.
- Source :
-
Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2019 May 01; Vol. 60 (6), pp. 2049-2063. - Publication Year :
- 2019
-
Abstract
- Purpose: To assess the phenotypic variability and natural course of inherited retinal diseases (IRDs) caused by EYS mutations.<br />Methods: Multiethnic cohort study (N = 30) with biallelic EYS variants from a clinical IRD database (retinitis pigmentosa [RP], N = 27; cone-rod dystrophy [CRD], N = 1; and macular dystrophy, N = 2). In vitro minigene splice assay was performed to determine the effect on EYS pre-mRNA splicing of the c.1299+5&#95;1299+8del variant in macular dystrophy patients.<br />Results: We found 27 different EYS variants in RP patients and 7 were novel. The rate of visual field loss of the V4e isopter area was -0.84 ± 0.44 ln(deg2) per year, and the rate of visual acuity loss was 0.75 Early Treatment Diabetic Retinopathy Study letters per year. Ellipsoid zone width was correlated with area of the hyperautofluorescent ring, with rs = 0.78 and P < 0.001. Rate of decline in ellipsoid zone width was -57 ± 17 μm per year (P < 0.01) (n = 14) or -3.69% ± 0.51% from baseline per year (P < 0.001). An isolated CRD patient carried a homozygous EYS variant (c.9405T>A), previously identified in RP patients. Two siblings with macular dystrophy carried compound heterozygous EYS variants: c.1299+5&#95;1299+8del and c.6050G>T. The former was novel and shown to result in skipping of exon 8, and the latter was a known RP variant.<br />Conclusions: We report on EYS-associated macular dystrophy, extending the spectrum of EYS-associated IRDs. We observed heterogeneity between RP patients in age of onset and disease progression. Identical EYS variants were found in cases with RP, CRD, and macular dystrophy. Screening for EYS variants in CRD and macular dystrophy patients might increase the diagnostic yield in previously unsolved cases.
- Subjects :
- Adult
Aged
Aged, 80 and over
DNA Mutational Analysis
Electroretinography
Eye Proteins metabolism
Female
Homozygote
Humans
Macular Degeneration diagnosis
Macular Degeneration metabolism
Male
Middle Aged
Pedigree
Phenotype
Retina metabolism
Retina physiopathology
Retinitis Pigmentosa diagnosis
Retinitis Pigmentosa metabolism
Tomography, Optical Coherence
Young Adult
Eye Proteins genetics
Macular Degeneration genetics
Mutation
RNA, Messenger genetics
Retina pathology
Retinitis Pigmentosa genetics
Visual Acuity
Subjects
Details
- Language :
- English
- ISSN :
- 1552-5783
- Volume :
- 60
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Investigative ophthalmology & visual science
- Publication Type :
- Academic Journal
- Accession number :
- 31074760
- Full Text :
- https://doi.org/10.1167/iovs.18-25531