Literature DB >> 16505054

Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism.

Daniel Barthelmes1, Florian K Sutter, Malaika M Kurz-Levin, Martina M Bosch, Horst Helbig, Günter Niemeyer, Johannes C Fleischhauer.   

Abstract

PURPOSE: To quantify optical coherence tomography (OCT) images of the central retina in patients with blue-cone monochromatism (BCM) and achromatopsia (ACH) compared with healthy control individuals.
METHODS: The study included 15 patients with ACH, 6 with BCM, and 20 control subjects. Diagnosis of BCM and ACH was established by visual acuity testing, morphologic examination, color vision testing, and Ganzfeld ERG recording. OCT images were acquired with the Stratus OCT 3 (Carl Zeiss Meditec AG, Oberkochen, Germany). Foveal OCT images were analyzed by calculating longitudinal reflectivity profiles (LRPs) from scan lines. Profiles were analyzed quantitatively to determine foveal thickness and distances between reflectivity layers.
RESULTS: Patients with ACH and BCM had a mean visual acuity of 20/200 and 20/60, respectively. Color vision testing results were characteristic of the diseases. The LRPs of control subjects yielded four peaks (P1-P4), presumably representing the RPE (P1), the ovoid region of the photoreceptors (P2), the external limiting membrane (ELM) (P3), and the internal limiting membrane (P4). In patients with ACH, P2 was absent, but foveal thickness (P1-P4) did not differ significantly from that in the control subjects (187 +/- 20 vs. 192 +/- 14 microm, respectively). The distance from P1 to P3 did not differ significantly (78 +/- 10 vs. 82 +/- 5 microm) between ACH and controls subjects. In patients with BCM, P3 was lacking, and P2 advanced toward P1 compared with the control subjects (32 +/- 6 vs. 48 +/- 4 microm). Foveal thickness (153 +/- 16 microm) was significantly reduced compared with that in control subjects and patients with ACH.
CONCLUSIONS: Quantitative OCT image analysis reveals distinct patterns for controls subjects and patients with ACH and BCM, respectively. Quantitative analysis of OCT imaging can be useful in differentiating retinal diseases affecting photoreceptors. Foveal thickness is similar in both normal subjects and patients with ACH but is decreased in patients with BCM.

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Year:  2006        PMID: 16505054     DOI: 10.1167/iovs.05-0783

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


  28 in total

1.  The inner segment/outer segment border seen on optical coherence tomography is less intense in patients with diminished cone function.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2011-12-28       Impact factor: 4.799

2.  Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.

Authors:  M Sustar; D Perovšek; I Cima; B Stirn-Kranjc; M Hawlina; J Brecelj
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3.  Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.

Authors:  David G Birch; Yuquan Wen; Kelly Locke; Donald C Hood
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-09-09       Impact factor: 4.799

4.  Structural and functional correlates in color vision deficiency.

Authors:  A Gupta; G Laxmi; M G Nittala; R Raman
Journal:  Eye (Lond)       Date:  2011-04-15       Impact factor: 3.775

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Authors:  Nripun Sredar; Moataz Razeen; Bartlomiej Kowalski; Joseph Carroll; Alfredo Dubra
Journal:  Biomed Opt Express       Date:  2021-01-08       Impact factor: 3.732

6.  Multimodal imaging of foveal cavitation in retinal dystrophies.

Authors:  Maurizio Battaglia Parodi; Maria Vittoria Cicinelli; Pierluigi Iacono; Gianluigi Bolognesi; Francesco Bandello
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2016-08-05       Impact factor: 3.117

7.  Tomographic comparison of cone-rod and rod-cone retinal dystrophies.

Authors:  Emiko Inui; Akio Oishi; Maho Oishi; Ken Ogino; Yukiko Makiyama; Norimoto Gotoh; Masafumi Kurimoto; Nagahisa Yoshimura
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8.  The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.

Authors:  Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G Robson; Graham E Holder; Keith Bradshaw; David M Hunt; Andrew R Webster; Anthony T Moore; Daniel F Schorderet; Francis L Munier
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-04-14       Impact factor: 4.799

9.  Retinal findings in a patient of French ancestry with CABP4-related retinal disease.

Authors:  Vasily Mikhaïlovitch Smirnov; Christina Zeitz; Nagasamy Soumittra; Isabelle Audo; Sabine Defoort-Dhellemmes
Journal:  Doc Ophthalmol       Date:  2018-03-10       Impact factor: 2.379

10.  Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Tomas S Aleman; Alexander Sumaroka; Elizabeth A M Windsor; Sharon B Schwartz; Elise Heon; Edwin M Stone
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-06-06       Impact factor: 4.799

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