Literature DB >> 25425308

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

Wadih M Zein1, Benedetto Falsini1, Ekaterina T Tsilou1, Amy E Turriff1, Julie M Schultz2, Thomas B Friedman2, Carmen C Brewer3, Christopher K Zalewski3, Kelly A King3, Julie A Muskett3, Atteeq U Rehman2, Robert J Morell2, Andrew J Griffith3, Paul A Sieving4.   

Abstract

PURPOSE: Progressive decline of psychophysical cone-mediated measures has been reported in type 1 (USH1) and type 2 (USH2) Usher syndrome. Conventional cone electroretinogram (ERG) responses in USH demonstrate poor signal-to-noise ratio. We evaluated cone signals in USH1 and USH2 by recording microvolt level cycle-by-cycle (CxC) ERG.
METHODS: Responses of molecularly genotyped USH1 (n = 18) and USH2 (n = 24) subjects (age range, 15-69 years) were compared with those of controls (n = 12). A subset of USH1 (n = 9) and USH2 (n = 9) subjects was examined two to four times over 2 to 8 years. Photopic CxC ERG and conventional 30-Hz flicker ERG were recorded on the same visits.
RESULTS: Usher syndrome subjects showed considerable cone flicker ERG amplitude losses and timing phase delays (P < 0.01) compared with controls. USH1 and USH2 had similar rates of progressive logarithmic ERG amplitude decline with disease duration (-0.012 log μV/y). Of interest, ERG phase delays did not progress over time. Two USH1C subjects retained normal response timing despite reduced amplitudes. The CxC ERG method provided reliable responses in all subjects, whereas conventional ERG was undetectable in 7 of 42 subjects.
CONCLUSIONS: Cycle-by-cycle ERG showed progressive loss of amplitude in both USH1 and USH2 subjects, comparable to that reported with psychophysical measures. Usher subjects showed abnormal ERG response latency, but this changed less than amplitude with time. In USH syndrome, CxC ERG is more sensitive than conventional ERG and warrants consideration as an outcome measure in USH treatment trials. Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.

Entities:  

Keywords:  Usher genes; Usher syndrome; cone function; microvolt electroretinogram

Mesh:

Year:  2014        PMID: 25425308      PMCID: PMC4288141          DOI: 10.1167/iovs.14-15355

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


  32 in total

1.  Phenotypes in defined genotypes including siblings with Usher syndrome.

Authors:  Eva Malm; Vesna Ponjavic; Claes Möller; William J Kimberling; Sten Andréasson
Journal:  Ophthalmic Genet       Date:  2010-12-21       Impact factor: 1.803

2.  Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.

Authors:  Atteeq U Rehman; Regie Lyn P Santos-Cortez; Robert J Morell; Meghan C Drummond; Taku Ito; Kwanghyuk Lee; Asma A Khan; Muhammad Asim R Basra; Naveed Wasif; Muhammad Ayub; Rana A Ali; Syed I Raza; Deborah A Nickerson; Jay Shendure; Michael Bamshad; Saima Riazuddin; Neil Billington; Shaheen N Khan; Penelope L Friedman; Andrew J Griffith; Wasim Ahmad; Sheikh Riazuddin; Suzanne M Leal; Thomas B Friedman
Journal:  Am J Hum Genet       Date:  2014-01-02       Impact factor: 11.025

3.  Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Dan Gibbs; Alexander Sumaroka; Alejandro J Roman; Tomas S Aleman; Sharon B Schwartz; Melani B Olivares; Robert C Russell; Janet D Steinberg; Margaret A Kenna; William J Kimberling; Heidi L Rehm; David S Williams
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-10-07       Impact factor: 4.799

4.  Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype.

Authors:  Sharon B Schwartz; Tomas S Aleman; Artur V Cideciyan; Elizabeth A M Windsor; Alexander Sumaroka; Alejandro J Roman; Tej Rane; Elaine E Smilko; Jean Bennett; Edwin M Stone; William J Kimberling; Xue-Zhong Liu; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-02       Impact factor: 4.799

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Authors:  Dominic Cosgrove; Marisa Zallocchi
Journal:  Int J Biochem Cell Biol       Date:  2013-11-12       Impact factor: 5.085

6.  Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2.

Authors:  Ana Fakin; Martina Jarc-Vidmar; Damjan Glavač; Crystel Bonnet; Christine Petit; Marko Hawlina
Journal:  Vision Res       Date:  2012-09-18       Impact factor: 1.886

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

Authors:  Michael A Sandberg; Bernard Rosner; Carol Weigel-DiFranco; Terri L McGee; Thaddeus P Dryja; Eliot L Berson
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-07-18       Impact factor: 4.799

8.  Kinetics of visual field loss in Usher syndrome Type II.

Authors:  Alessandro Iannaccone; Stephen B Kritchevsky; Maria Laura Ciccarelli; Salvatore A Tedesco; Claudio Macaluso; William J Kimberling; Grant W Somes
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-03       Impact factor: 4.799

9.  Development of a genotyping microarray for Usher syndrome.

Authors:  Frans P M Cremers; William J Kimberling; Maigi Külm; Arjan P de Brouwer; Erwin van Wijk; Heleen te Brinke; Cor W R J Cremers; Lies H Hoefsloot; Sandro Banfi; Francesca Simonelli; Johannes C Fleischhauer; Wolfgang Berger; Phil M Kelley; Elene Haralambous; Maria Bitner-Glindzicz; Andrew R Webster; Zubin Saihan; Elfride De Baere; Bart P Leroy; Giuliana Silvestri; Gareth J McKay; Robert K Koenekoop; Jose M Millan; Thomas Rosenberg; Tarja Joensuu; Eeva-Marja Sankila; Dominique Weil; Mike D Weston; Bernd Wissinger; Hannie Kremer
Journal:  J Med Genet       Date:  2006-09-08       Impact factor: 6.318

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  6 in total

1.  A method for estimating intrinsic noise in electroretinographic (ERG) signals.

Authors:  Andrew J Zele; Beatrix Feigl; Pradeep K Kambhampati; Amithavikram R Hathibelagal; Jan Kremers
Journal:  Doc Ophthalmol       Date:  2015-08-19       Impact factor: 2.379

2.  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

3.  Recessive mutations of TMC1 associated with moderate to severe hearing loss.

Authors:  Ayesha Imtiaz; Azra Maqsood; Atteeq U Rehman; Robert J Morell; Jeffrey R Holt; Thomas B Friedman; Sadaf Naz
Journal:  Neurogenetics       Date:  2016-02-16       Impact factor: 2.660

4.  Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.

Authors:  Elodie M Richard; Regie Lyn P Santos-Cortez; Rabia Faridi; Atteeq U Rehman; Kwanghyuk Lee; Mohsin Shahzad; Anushree Acharya; Asma A Khan; Ayesha Imtiaz; Imen Chakchouk; Christina Takla; Izoduwa Abbe; Maria Rafeeq; Khurram Liaqat; Taimur Chaudhry; Michael J Bamshad; Deborah A Nickerson; Isabelle Schrauwen; Shaheen N Khan; Robert J Morell; Saba Zafar; Muhammad Ansar; Zubair M Ahmed; Wasim Ahmad; Sheikh Riazuddin; Thomas B Friedman; Suzanne M Leal; Saima Riazuddin
Journal:  Hum Mutat       Date:  2018-11-18       Impact factor: 4.878

5.  [Screening for ocular involvement in deaf children].

Authors:  Belghmaidi Sarah; Belhoucha Btissam; Hajji Ibtissam; Rochdi Youssef; Albab Nabil; Nouri Hassan; Aderdour Lahcen; Raji Abdelaziz; Moutaouakil Abdeljalil
Journal:  Pan Afr Med J       Date:  2019-07-05

6.  Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments.

Authors:  Alix Trouillet; Elisabeth Dubus; Julie Dégardin; Amrit Estivalet; Ivana Ivkovic; David Godefroy; Diego García-Ayuso; Manuel Simonutti; Iman Sahly; José A Sahel; Aziz El-Amraoui; Christine Petit; Serge Picaud
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  6 in total

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