Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data
- PMID: 19376587
- DOI: 10.1016/j.ophtha.2009.01.016
Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data
Abstract
Purpose: To describe fundus autofluorescence (FAF) in carriers of choroideremia (CHM), and to compare FAF findings with ophthalmoscopy and electrophysiologic and psychophysical data.
Design: Prospective, observational case series and systematic review.
Participants: Six unrelated carriers of CHM.
Methods: Clinical examination included a comprehensive ophthalmic examination, fundus photography, FAF, kinetic perimetry, 2-color threshold perimetry (2CTP), full-field electroretinography (ERG), and multifocal ERG (mfERG). All 6 carriers (33-60 years of age) were screened for mutations in the coding region of Rab Escort Protein 1 gene (REP1) including close flanking intronic sequence and deletions within 2160 bp of 5' untranslated sequence.
Main outcome measures: Intensity and distribution of FAF, rod sensitivity loss, cone sensitivity loss in 2CTP, amplitude and latency in full-field ERG, amplitude in mfERG, and correlation of all 3 parameters.
Results: Mutations in the coding region of REP1 were identified in 3 of 6 carriers. All 6 carriers had good visual acuity. Three carriers complained of photophobia and 1 of impaired vision in dim light. Ophthalmoscopy revealed peripapillary atrophy and retinal pigment epithelium (RPE) mottling mainly in the macular region, and additional RPE clumping and flecks of atrophy in the periphery. A very irregular pattern of low- and high-density FAF speckles was seen. Low-density FAF surrounding the optic nerve head corresponded with the peripapillary atrophy. In areas of major FAF changes, mfERG was deteriorated. The 2CTP images revealed functional disturbances in rods and cones. No general pattern was observed. On MfERG, reduced amplitudes in areas with normal cone sensitivity in 2CTP were seen.
Conclusions: All 6 carriers of CHM showed a characteristic FAF pattern that can guide mutation analysis. Even when other functional testing is inconspicuous, FAF is a rapid, noninvasive indicator.
Financial disclosure(s): The authors have no proprietary or commercial interest in any of the materials discussed in this article.
Similar articles
-
Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.Ophthalmology. 2006 Nov;113(11):2066.e1-10. doi: 10.1016/j.ophtha.2006.05.045. Epub 2006 Aug 28. Ophthalmology. 2006. PMID: 16935340
-
Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing.Ophthalmology. 2008 Apr;115(4):723-9. doi: 10.1016/j.ophtha.2007.07.032. Epub 2008 Jan 16. Ophthalmology. 2008. PMID: 18201765
-
Syndromic choroideremia: sublocalization of phenotypes associated with Martin-Probst deafness mental retardation syndrome.Invest Ophthalmol Vis Sci. 2008 Sep;49(9):4096-104. doi: 10.1167/iovs.08-2044. Epub 2008 May 16. Invest Ophthalmol Vis Sci. 2008. PMID: 18487380
-
Alström syndrome--a case report and literature review.Klin Oczna. 2008;110(4-6):188-92. Klin Oczna. 2008. PMID: 18655459 Review.
-
Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.Ophthalmology. 2007 Jul;114(7):1348-1357.e1. doi: 10.1016/j.ophtha.2006.10.034. Epub 2007 Feb 22. Ophthalmology. 2007. PMID: 17320181
Cited by
-
Single-Shot Ultra-Widefield Polarization-Diversity Optical Coherence Tomography for Assessing Retinal and Choroidal Pathologies.J Clin Med. 2024 Sep 12;13(18):5415. doi: 10.3390/jcm13185415. J Clin Med. 2024. PMID: 39336902 Free PMC article.
-
High-resolution images of retinal structure in patients with choroideremia.Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):950-61. doi: 10.1167/iovs.12-10707. Invest Ophthalmol Vis Sci. 2013. PMID: 23299470 Free PMC article.
-
Patterns and Intensities of Near-Infrared and Short-Wavelength Fundus Autofluorescence in Choroideremia Probands and Carriers.Invest Ophthalmol Vis Sci. 2019 Sep 3;60(12):3752-3761. doi: 10.1167/iovs.19-27366. Invest Ophthalmol Vis Sci. 2019. PMID: 31499530 Free PMC article.
-
Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.Doc Ophthalmol. 2012 Aug;125(1):81-9. doi: 10.1007/s10633-012-9335-0. Epub 2012 Jun 7. Doc Ophthalmol. 2012. PMID: 22674428
-
Choroideremia Carriers: Dark-Adapted Perimetry and Retinal Structures.Invest Ophthalmol Vis Sci. 2022 Jul 8;63(8):4. doi: 10.1167/iovs.63.8.4. Invest Ophthalmol Vis Sci. 2022. PMID: 35816046 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials