Literature DB >> 18641288

Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.

Michael A Sandberg1, Bernard Rosner, Carol Weigel-DiFranco, Terri L McGee, Thaddeus P Dryja, Eliot L Berson.   

Abstract

PURPOSE: To estimate the mean rates of ocular function loss in patients with autosomal recessive retinitis pigmentosa due to USH2A mutations.
METHODS: In 125 patients with USH2A mutations, longitudinal regression was used to estimate mean rates of change in Snellen visual acuity, Goldmann visual field area (V4e white test light), and 30-Hz (cone) full-field electroretinogram amplitude. These rates were compared with those of previously studied cohorts with dominant retinitis pigmentosa due to RHO mutations and with X-linked retinitis pigmentosa due to RPGR mutations. Rates of change in patients with the Cys759Phe mutation, the USH2A mutation associated with nonsyndromic disease, were compared with rates of change in patients with the Glu767fs mutation, the most common USH2A mutation associated with Usher syndrome type II (i.e., retinitis pigmentosa and hearing loss).
RESULTS: Mean annual exponential rates of decline for the USH2A patients were 2.6% for visual acuity, 7.0% for visual field area, and 13.2% for electroretinogram amplitude. The rate of acuity loss fell between the corresponding rates for the RHO and RPGR patients, whereas the rates for field and ERG amplitude loss were faster than those for the RHO and RPGR patients. No significant differences were found for patients with the Cys759Phe mutation versus patients with the Glu767fs mutation.
CONCLUSIONS: On average, USH2A patients lose visual acuity faster than RHO patients and slower than RPGR patients. USH2A patients lose visual field and cone electroretinogram amplitude faster than patients with RHO or RPGR mutations. Patients with a nonsyndromic USH2A mutation have the same retinal disease course as patients with syndromic USH2A disease.

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Year:  2008        PMID: 18641288      PMCID: PMC2588642          DOI: 10.1167/iovs.08-2009

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


  14 in total

1.  Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variation.

Authors:  S Bernal; C Ayuso; G Antiñolo; A Gimenez; S Borrego; M J Trujillo; I Marcos; M Calaf; E Del Rio; M Baiget
Journal:  J Med Genet       Date:  2003-01       Impact factor: 6.318

2.  Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.

Authors:  C Rivolta; E A Sweklo; E L Berson; T P Dryja
Journal:  Am J Hum Genet       Date:  2000-04-20       Impact factor: 11.025

3.  A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.

Authors:  B Dreyer; L Tranebjaerg; V Brox; T Rosenberg; C Möller; M Beneyto; M D Weston; W J Kimberling; C W Cremers; X Z Liu; O Nilssen
Journal:  Am J Hum Genet       Date:  2001-06-08       Impact factor: 11.025

4.  Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

Authors:  M D Weston; J D Eudy; S Fujita; S Yao; S Usami; C Cremers; J Greenberg; R Ramesar; A Martini; C Moller; R J Smith; J Sumegi; W J Kimberling; J Greenburg
Journal:  Am J Hum Genet       Date:  2000-03-22       Impact factor: 11.025

5.  Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.

Authors:  T P Dryja; J A McEvoy; T L McGee; E L Berson
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-09       Impact factor: 4.799

6.  Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

Authors:  J D Eudy; M D Weston; S Yao; D M Hoover; H L Rehm; M Ma-Edmonds; D Yan; I Ahmad; J J Cheng; C Ayuso; C Cremers; S Davenport; C Moller; C B Talmadge; K W Beisel; M Tamayo; C C Morton; A Swaroop; W J Kimberling; J Sumegi
Journal:  Science       Date:  1998-06-12       Impact factor: 47.728

7.  Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.

Authors:  Babak Jian Seyedahmadi; Carlo Rivolta; Julia A Keene; Eliot L Berson; Thaddeus P Dryja
Journal:  Exp Eye Res       Date:  2004-08       Impact factor: 3.467

8.  RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.

Authors:  Dror Sharon; Michael A Sandberg; Vivian W Rabe; Melissa Stillberger; Thaddeus P Dryja; Eliot L Berson
Journal:  Am J Hum Genet       Date:  2003-10-16       Impact factor: 11.025

9.  Natural course of visual field loss in patients with Type 2 Usher syndrome.

Authors:  Gerald A Fishman; Simge Bozbeyoglu; Robert W Massof; William Kimberling
Journal:  Retina       Date:  2007-06       Impact factor: 4.256

10.  Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2a.

Authors:  Ronald J E Pennings; Patrick L M Huygen; Dana J Orten; Mariette Wagenaar; Annelies van Aarem; Hannie Kremer; William J Kimberling; Cor W R J Cremers; August F Deutman
Journal:  Acta Ophthalmol Scand       Date:  2004-04
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  38 in total

1.  Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

Authors:  Terri L McGee; Babak Jian Seyedahmadi; Meredith O Sweeney; Thaddeus P Dryja; Eliot L Berson
Journal:  J Med Genet       Date:  2010-05-27       Impact factor: 6.318

2.  Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

Authors:  Wadih M Zein; Benedetto Falsini; Ekaterina T Tsilou; Amy E Turriff; Julie M Schultz; Thomas B Friedman; Carmen C Brewer; Christopher K Zalewski; Kelly A King; Julie A Muskett; Atteeq U Rehman; Robert J Morell; Andrew J Griffith; Paul A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-11-25       Impact factor: 4.799

3.  Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study.

Authors:  Katarina Stingl; Anne Kurtenbach; Gesa Hahn; Christoph Kernstock; Stephanie Hipp; Ditta Zobor; Susanne Kohl; Crystel Bonnet; Saddek Mohand-Saïd; Isabelle Audo; Ana Fakin; Marko Hawlina; Francesco Testa; Francesca Simonelli; Christine Petit; Jose-Alain Sahel; Eberhart Zrenner
Journal:  Doc Ophthalmol       Date:  2019-07-02       Impact factor: 2.379

4.  Disease course of patients with unilateral pigmentary retinopathy.

Authors:  Emorfily Potsidis; Eliot L Berson; Michael A Sandberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-11-29       Impact factor: 4.799

5.  Association of Vitamin A Supplementation With Disease Course in Children With Retinitis Pigmentosa.

Authors:  Eliot L Berson; Carol Weigel-DiFranco; Bernard Rosner; Alexander R Gaudio; Michael A Sandberg
Journal:  JAMA Ophthalmol       Date:  2018-05-01       Impact factor: 7.389

6.  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

7.  Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis Pigmentosa.

Authors:  Tharikarn Sujirakul; Michael K Lin; Jimmy Duong; Ying Wei; Sara Lopez-Pintado; Stephen H Tsang
Journal:  Am J Ophthalmol       Date:  2015-07-09       Impact factor: 5.258

8.  PDZD7 and hearing loss: More than just a modifier.

Authors:  Kevin T Booth; Hela Azaiez; Kimia Kahrizi; Allen C Simpson; William T A Tollefson; Christina M Sloan; Nicole C Meyer; Mojgan Babanejad; Fariba Ardalani; Sanaz Arzhangi; Michael J Schnieders; Hossein Najmabadi; Richard J H Smith
Journal:  Am J Med Genet A       Date:  2015-09-29       Impact factor: 2.802

9.  Usherin defects lead to early-onset retinal dysfunction in zebrafish.

Authors:  Margo Dona; Ralph Slijkerman; Kimberly Lerner; Sanne Broekman; Jeremy Wegner; Taylor Howat; Theo Peters; Lisette Hetterschijt; Nanda Boon; Erik de Vrieze; Nasrin Sorusch; Uwe Wolfrum; Hannie Kremer; Stephan Neuhauss; Jingjing Zang; Maarten Kamermans; Monte Westerfield; Jennifer Phillips; Erwin van Wijk
Journal:  Exp Eye Res       Date:  2018-05-16       Impact factor: 3.467

10.  The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.

Authors:  Yang Zhao; Katsuhiro Hosono; Kimiko Suto; Chie Ishigami; Yuuki Arai; Akiko Hikoya; Yasuhiko Hirami; Masafumi Ohtsubo; Shinji Ueno; Hiroko Terasaki; Miho Sato; Hiroshi Nakanishi; Shiori Endo; Kunihiro Mizuta; Hiroyuki Mineta; Mineo Kondo; Masayo Takahashi; Shinsei Minoshima; Yoshihiro Hotta
Journal:  J Hum Genet       Date:  2014-07-31       Impact factor: 3.172

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