Literature DB >> 12888054

Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23.

Kean T Oh1, Reid Longmuir, Dawn M Oh, Edwin M Stone, Kelly Kopp, Jeremiah Brown, Gerald A Fishman, Peter Sonkin, Karen M Gehrs, Richard G Weleber.   

Abstract

PURPOSE: To examine the difference in expression of retinitis pigmentosa from mutations at codon 23 and codon 347 or rhodopsin; to report a novel mutation in rhodopsin.
METHODS: Goldmann perimetry (solid angle of I4e isopter) and electroretinographic amplitudes (square root transform of a response ratio) were analyzed for 24 patients with mutations at codon 347 (15 with Pro347Ala, 2 with Pro347Gln, 6 with Pro347Leu, and 1 with a novel Pro347Cys change) and 41 patients with mutations at codon 23 (6 with Pro23Ala; 35 with Pro23His).
RESULTS: When all patients with mutations at codons 347 and 23 were compared, loss of visual fields was significantly worse in patients with codon 347 changes (P =.0003). Only rod responses of the electroretinograms were significantly different between the two groups (P =.048). Specific comparison of Pro347Ala with Pro23Ala using regression analysis demonstrated significant differences in severity between codon 23 and codon 347 patients for b-wave amplitudes of rod (P =.0069), cone (P =.039) and maximum combined response (P =.049). The solid angle of the I4e isopter was also significantly different (P =.025) between the groups after controlling for age. Modeling age by group for Pro347Ala comparison produced an R(2) of.44.
CONCLUSION: We reconfirmed that rhodopsin-related retinitis pigmentosa from mutations involving codon 347 produces a more severe phenotype than that involving codon 23. Accurate modeling of disease was shown to be possible by incorporating the effects of a patient's age and specific genotype. Therefore, both of these variables must be considered in prognostic counseling and subject recruitment for future therapeutic trials.

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Year:  2003        PMID: 12888054     DOI: 10.1016/s0002-9394(03)00206-x

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  17 in total

1.  Pharmacological dissection of multifocal electroretinograms of rabbits with Pro347Leu rhodopsin mutation.

Authors:  Daisuke Yokoyama; Shigeki Machida; Mineo Kondo; Hiroko Terasaki; Tomoharu Nishimura; Daijiro Kurosaka
Journal:  Jpn J Ophthalmol       Date:  2010-11-05       Impact factor: 2.447

2.  Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.

Authors:  Edwin M Stone; Xunda Luo; Elise Héon; Byron L Lam; Richard G Weleber; Jennifer A Halder; Louisa M Affatigato; Jacqueline B Goldberg; Alexander Sumaroka; Sharon B Schwartz; Artur V Cideciyan; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-12-28       Impact factor: 4.799

3.  Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.

Authors:  Sanae Sakami; Tadao Maeda; Grzegorz Bereta; Kiichiro Okano; Marcin Golczak; Alexander Sumaroka; Alejandro J Roman; Artur V Cideciyan; Samuel G Jacobson; Krzysztof Palczewski
Journal:  J Biol Chem       Date:  2011-01-11       Impact factor: 5.157

4.  Cell Death Pathways in Mutant Rhodopsin Rat Models Identifies Genotype-Specific Targets Controlling Retinal Degeneration.

Authors:  Ishaq A Viringipurampeer; Cheryl Y Gregory-Evans; Andrew L Metcalfe; Emran Bashar; Orson L Moritz; Kevin Gregory-Evans
Journal:  Mol Neurobiol       Date:  2018-06-18       Impact factor: 5.590

5.  Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration.

Authors:  Francis Concepcion; Jeannie Chen
Journal:  PLoS One       Date:  2010-06-02       Impact factor: 3.240

6.  Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients.

Authors:  Isabelle Audo; Gaël Manes; Saddek Mohand-Saïd; Anne Friedrich; Marie-Elise Lancelot; Aline Antonio; Veselina Moskova-Doumanova; Oliver Poch; Xavier Zanlonghi; Christian P Hamel; José-Alain Sahel; Shomi S Bhattacharya; Christina Zeitz
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-02-17       Impact factor: 4.799

7.  Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosa.

Authors:  K T Oh; D M Oh; R G Weleber; E M Stone; A Parikh; J White; K A Deboer-Shields; L Streb; C Vallar
Journal:  Br J Ophthalmol       Date:  2004-12       Impact factor: 4.638

8.  Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Authors:  Vera L Bonilha; Mary E Rayborn; Brent A Bell; Meghan J Marino; Craig D Beight; Gayle J Pauer; Elias I Traboulsi; Joe G Hollyfield; Stephanie A Hagstrom
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-07-23       Impact factor: 3.117

9.  Calpain and PARP activation during photoreceptor cell death in P23H and S334ter rhodopsin mutant rats.

Authors:  Jasvir Kaur; Stine Mencl; Ayse Sahaboglu; Pietro Farinelli; Theo van Veen; Eberhart Zrenner; Per Ekström; François Paquet-Durand; Blanca Arango-Gonzalez
Journal:  PLoS One       Date:  2011-07-12       Impact factor: 3.240

10.  Identification of two mutations of the RHO gene in two Chinese families with retinitis pigmentosa: correlation between genotype and phenotype.

Authors:  Zhe Pan; Tingting Lu; Xiaohui Zhang; Hanjun Dai; Weiyu Yan; Fengge Bai; Yang Li
Journal:  Mol Vis       Date:  2012-12-14       Impact factor: 2.367

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