Literature DB >> 20720228

The transition zone between healthy and diseased retina in patients with retinitis pigmentosa.

Donald C Hood1, Margot A Lazow, Kirsten G Locke, Vivienne C Greenstein, David G Birch.   

Abstract

PURPOSE: To describe the structural changes in the transition zone from relatively healthy retinal regions to severely affected regions in patients with retinitis pigmentosa (RP) using frequency domain optical coherence tomography (fdOCT).
METHODS: FdOCT line scans of the horizontal meridian were obtained from one eye of 13 patients with RP and 30 control subjects. The patients had normal or near normal foveal sensitivities and visual field diameters ≥10°. Using a computer-aided manual segmentation procedure, the locations at which the outer segment (OS) and outer nuclear layer plus outer plexiform layer (ONL+) thicknesses fell below the 95% confidence interval of the controls were measured, as were the locations at which the OS layer disappeared and the locations at which the ONL+ was reduced to an asymptotically small thickness.
RESULTS: The progression from healthy to severely affected regions followed a common pattern in most patients. Region A, the central region including the foveal center, had normal OS and ONL+ thickness. Region B had abnormal OS but normal ONL+ thickness. Region C had abnormal but measurable OS and ONL+ thicknesses. In Region D, the OS layer disappeared, as did the IS/OS line, and the ONL+ thickness decreased further. In Region E, the ONL+ reached an asymptotic thickness.
CONCLUSIONS: The structural changes in the transition zone followed an orderly progression from a thinning of the OS layer, to a thinning of the ONL+, to a loss of the OS layer, to an ONL+ reduced to an asymptotically small level.

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Year:  2011        PMID: 20720228      PMCID: PMC3053270          DOI: 10.1167/iovs.10-5799

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


  14 in total

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2.  Interpretation of fovea center morphologic features in optical coherence tomography.

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Review 3.  Histopathology of the human retina in retinitis pigmentosa.

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4.  Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-18       Impact factor: 11.205

5.  A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa.

Authors:  Nalini V Rangaswamy; Hemaxi M Patel; Kirsten G Locke; Donald C Hood; David G Birch
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-03-10       Impact factor: 4.799

6.  Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2008-04       Impact factor: 4.799

7.  Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Authors:  Tomas S Aleman; Artur V Cideciyan; Alexander Sumaroka; Sharon B Schwartz; Alejandro J Roman; Elizabeth A M Windsor; Janet D Steinberg; Kari Branham; Mohammad Othman; Anand Swaroop; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-10       Impact factor: 4.799

8.  Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis.

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9.  Structural assessment of hyperautofluorescent ring in patients with retinitis pigmentosa.

Authors:  Luiz H Lima; Wener Cella; Vivienne C Greenstein; Nan-Kai Wang; Mihai Busuioc; R Theodore Smith; Lawrence A Yannuzzi; Stephen H Tsang
Journal:  Retina       Date:  2009 Jul-Aug       Impact factor: 4.256

10.  Normal central retinal function and structure preserved in retinitis pigmentosa.

Authors:  Samuel G Jacobson; Alejandro J Roman; Tomas S Aleman; Alexander Sumaroka; Waldo Herrera; Elizabeth A M Windsor; Lori A Atkinson; Sharon B Schwartz; Janet D Steinberg; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-09-24       Impact factor: 4.799

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  63 in total

1.  Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP).

Authors:  Margot A Lazow; Donald C Hood; Rithambara Ramachandran; Tomas R Burke; Yi-Zhong Wang; Vivienne C Greenstein; David G Birch
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-12-20       Impact factor: 4.799

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

Authors:  Donald C Hood; Xian Zhang; Rithambara Ramachandran; Christine L Talamini; Ali Raza; Jonathan P Greenberg; Jerome Sherman; Stephen H Tsang; David G Birch
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-12-28       Impact factor: 4.799

3.  Automated segmentation of intramacular layers in Fourier domain optical coherence tomography structural images from normal subjects.

Authors:  Xusheng Zhang; Siavash Yousefi; Lin An; Ruikang K Wang
Journal:  J Biomed Opt       Date:  2012-04       Impact factor: 3.170

4.  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

5.  Structural and functional changes associated with normal and abnormal fundus autofluorescence in patients with retinitis pigmentosa.

Authors:  Vivienne C Greenstein; Tobias Duncker; Karen Holopigian; Ronald E Carr; Jonathan P Greenberg; Stephen H Tsang; Donald C Hood
Journal:  Retina       Date:  2012-02       Impact factor: 4.256

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

Authors:  Moreno Menghini; Brandon J Lujan; Shiri Zayit-Soudry; Reema Syed; Travis C Porco; Kristine Bayabo; Joseph Carroll; Austin Roorda; Jacque L Duncan
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-12-16       Impact factor: 4.799

7.  Correlation between B-scan optical coherence tomography, en face thickness map ring and hyperautofluorescent ring in retinitis pigmentosa patients.

Authors:  Vitor K L Takahashi; Júlia T Takiuti; Ruben Jauregui; Christine L Xu; Jimmy K Duong; Luiz H Lima; Stephen H Tsang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2019-05-02       Impact factor: 3.117

8.  Outer retinal layers as predictors of visual acuity in retinitis pigmentosa: a cross-sectional study.

Authors:  Keissy Sousa; Tiago Fernandes; Rita Gentil; Luís Mendonça; Manuel Falcão
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2018-11-19       Impact factor: 3.117

9.  Association between multifocal electroretinograms, optical coherence tomography and central visual sensitivity in advanced retinitis pigmentosa.

Authors:  Chan Hee Moon; Tae Kwann Park; Young-Hoon Ohn
Journal:  Doc Ophthalmol       Date:  2012-08-03       Impact factor: 2.379

10.  Optical coherence tomography biomarkers of photoreceptor degeneration in retinitis pigmentosa.

Authors:  Yuting Gong; Honghe Xia; Anlin Zhang; Li Jia Chen; Haoyu Chen
Journal:  Int Ophthalmol       Date:  2021-07-25       Impact factor: 2.031

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