Literature DB >> 21071739

Cone structure in retinal degeneration associated with mutations in the peripherin/RDS gene.

Jacque L Duncan1, Katherine E Talcott, Kavitha Ratnam, Sanna M Sundquist, Anya S Lucero, Shelley Day, Yuhua Zhang, Austin Roorda.   

Abstract

PURPOSE: To study cone photoreceptor structure and function associated with mutations in the second intradiscal loop region of peripherin/RDS.
METHODS: High-resolution macular images were obtained with adaptive optics scanning laser ophthalmoscopy and spectral domain optical coherence tomography in four patients with peripherin/RDS mutations and 27 age-similar healthy subjects. Measures of retinal structure and fundus autofluorescence (AF) were correlated with visual function, including best-corrected visual acuity (BCVA), kinetic and static perimetry, fundus-guided microperimetry, full-field electroretinography (ERG), and multifocal ERG. The coding regions of the peripherin/RDS gene were sequenced in each patient.
RESULTS: Heterozygous mutations in peripherin/RDS were predicted to affect protein structure in the second intradiscal domain in each patient (Arg172Trp, Gly208Asp, Pro210Arg and Cys213Tyr). BCVA was at least 20/32 in the study eye of each patient. Diffuse cone-greater-than-rod dysfunction was present in patient 1, while rod-greater-than-cone dysfunction was present in patient 4; macular outer retinal dysfunction was present in all patients. Macular AF was heterogeneous, and the photoreceptor-retinal pigment epithelial (RPE) junction layer showed increased reflectivity at the fovea in all patients except patient 1, who showed cone-rod dystrophy. Cone packing was irregular, and cone spacing was significantly increased (z-scores >2) at most locations throughout the central 4° in each patient.
CONCLUSIONS: peripherin/RDS mutations produced diffuse AF abnormalities, disruption of the photoreceptor/RPE junction, and increased cone spacing, consistent with cone loss in the macula. The abnormalities observed suggest that the integrity of the second intradiscal domain of peripherin/RDS is critical for normal macular cone structure.

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Year:  2011        PMID: 21071739      PMCID: PMC3101697          DOI: 10.1167/iovs.10-6549

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  52 in total

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7.  Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families.

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8.  Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.

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  31 in total

1.  Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations.

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2.  Correlation of outer nuclear layer thickness with cone density values in patients with retinitis pigmentosa and healthy subjects.

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3.  Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram".

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6.  Retinal imaging using adaptive optics technology.

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7.  Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2012-02-21       Impact factor: 4.799

8.  Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.

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10.  Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.

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