Literature DB >> 27409480

Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations.

Alexander Sumaroka, Rodrigo Matsui, Artur V Cideciyan, David B McGuigan, Rebecca Sheplock, Sharon B Schwartz, Samuel G Jacobson.   

Abstract

PURPOSE: To study transition zones from normal to abnormal retina in Usher syndrome IB (USH1B) caused by myosin 7A (MYO7A) mutations.
METHODS: Optical coherence tomography (OCT) scattering layers in outer retina were segmented in patients (n = 16, ages 2-42; eight patients had serial data, average interval 4.5 years) to quantify outer nuclear layer (ONL) and outer segments (OS) as well as the locus of EZ (ellipsoid zone) edge and its extent from the fovea. Static perimetry was measured under dark-adapted (DA) and light-adapted (LA) conditions.
RESULTS: Ellipsoid zone edge in USH1B-MYO7A could be located up to 23° from the fovea. Ellipsoid zone extent constricted at a rate of 0.51°/year with slower rates at smaller eccentricities. A well-defined EZ line could be associated with normal or abnormal ONL and/or OS thickness; detectable ONL extended well beyond EZ edge. At the EZ edge, the local slope of LA sensitivity loss was 2.6 (±1.7) dB/deg for central transition zones. At greater eccentricities, the local slope of cone sensitivity loss was shallower (1.1 ± 0.4 dB/deg for LA) than that of rod sensitivity loss (2.8 ± 1.2 dB/deg for DA).
CONCLUSIONS: In USH1B-MYO7A, constriction rate of EZ extent depends on the initial eccentricity of the transition. Ellipsoid zone edges in the macula correspond to large local changes in cone vision, but extramacular EZ edges show more pronounced losses on rod-based vision tests. It is advisable to use not only the EZ line but also other structural and functional parameters for estimating natural history of disease and possible therapeutic effects in future clinical trials of USH1B-MYO7A.

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Year:  2016        PMID: 27409480     DOI: 10.1167/iovs.15-18860

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


  9 in total

1.  EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression.

Authors:  David B McGuigan; Elise Heon; Artur V Cideciyan; Rinki Ratnapriya; Monica Lu; Alexander Sumaroka; Alejandro J Roman; Vaishnavi Batmanabane; Alexandra V Garafalo; Edwin M Stone; Anand Swaroop; Samuel G Jacobson
Journal:  Genes (Basel)       Date:  2017-07-12       Impact factor: 4.096

2.  Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence.

Authors:  Alexander Sumaroka; Alexandra V Garafalo; Evelyn P Semenov; Rebecca Sheplock; Arun K Krishnan; Alejandro J Roman; Samuel G Jacobson; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-06-03       Impact factor: 4.799

3.  Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes.

Authors:  Helena M Feenstra; Saoud Al-Khuzaei; Mital Shah; Suzanne Broadgate; Morag Shanks; Archith Kamath; Jing Yu; Jasleen K Jolly; Robert E MacLaren; Penny Clouston; Stephanie Halford; Susan M Downes
Journal:  Genes (Basel)       Date:  2022-08-10       Impact factor: 4.141

Review 4.  Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives.

Authors:  Alexandra V Garafalo; Artur V Cideciyan; Elise Héon; Rebecca Sheplock; Alexander Pearson; Caberry WeiYang Yu; Alexander Sumaroka; Gustavo D Aguirre; Samuel G Jacobson
Journal:  Prog Retin Eye Res       Date:  2019-12-30       Impact factor: 21.198

5.  Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.

Authors:  Samuel G Jacobson; David B McGuigan; Alexander Sumaroka; Alejandro J Roman; Michaela L Gruzensky; Rebecca Sheplock; Judy Palma; Sharon B Schwartz; Tomas S Aleman; Artur V Cideciyan
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-09-01       Impact factor: 4.799

6.  Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps.

Authors:  Jacque L Duncan; Eric A Pierce; Amy M Laster; Stephen P Daiger; David G Birch; John D Ash; Alessandro Iannaccone; John G Flannery; José A Sahel; Donald J Zack; Marco A Zarbin
Journal:  Transl Vis Sci Technol       Date:  2018-07-18       Impact factor: 3.283

7.  Autosomal Dominant Retinitis Pigmentosa Due to Class B Rhodopsin Mutations: An Objective Outcome for Future Treatment Trials.

Authors:  Alexander Sumaroka; Artur V Cideciyan; Jason Charng; Vivian Wu; Christian A Powers; Bhavya S Iyer; Brianna Lisi; Malgorzata Swider; Samuel G Jacobson
Journal:  Int J Mol Sci       Date:  2019-10-27       Impact factor: 5.923

8.  A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies.

Authors:  Kaitlyn R Calabro; Sanford L Boye; Shreyasi Choudhury; Diego Fajardo; James J Peterson; Wei Li; Sean M Crosson; Mi-Jung Kim; Dalian Ding; Richard Salvi; Shinichi Someya; Shannon E Boye
Journal:  Front Neurosci       Date:  2019-11-22       Impact factor: 5.152

Review 9.  Usher syndrome: clinical features, molecular genetics and advancing therapeutics.

Authors:  Maria Toms; Waheeda Pagarkar; Mariya Moosajee
Journal:  Ther Adv Ophthalmol       Date:  2020-09-17
  9 in total

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