Literature DB >> 30300311

PROGRESSION OF SCOTOPIC SINGLE-FLASH ELECTRORETINOGRAPHY IN THE STAGES OF CAPN5 VITREORETINOPATHY.

Peter H Tang1, Tyson R Kinnick2, James C Folk3, MaryAnn Mahajan1, Alexander G Bassuk4, Stephen H Tsang5,6, Vinit B Mahajan1,7.   

Abstract

PURPOSE: To characterize the changes found in the electroretinography (ERG) recordings of patients with autosomal dominant neovascular inflammatory vitreoretinopathy and correlate with clinical stages of the disease.
METHODS: Retrospective chart review. Bright- and dim-flash full-field scotopic, photopic, and 30-Hz flicker ERGs were obtained according to international standards. The scotopic ERGs were further processed to analyze the oscillatory potential. The patient described in the case report underwent full ERG testing; five patients composed the archival case series data and included scotopic ERG recordings.
RESULTS: Stage I autosomal dominant neovascular inflammatory vitreoretinopathy is characterized by a decrease in the b-wave amplitude on scotopic flash ERG and the disappearance of late OPs; however, the a-wave amplitude is normal. In Stage II, attenuation of early OPs and the c-wave are observed in scotopic ERG recordings, but both a- and b-wave amplitudes are unchanged. For patients in Stage III, there is a continued decline of both a- and b-wave amplitudes in scotopic ERG recordings. There was a loss of recordable scotopic ERG response in patients with Stage IV disease.
CONCLUSION: Electroretinography may be valuable in determining optimal timing for therapeutic intervention and response before loss of recordable retinal function in CAPN5 vitreoretinopathy.

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Year:  2021        PMID: 30300311      PMCID: PMC6453748          DOI: 10.1097/ICB.0000000000000828

Source DB:  PubMed          Journal:  Retin Cases Brief Rep        ISSN: 1935-1089


  18 in total

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Authors:  M Azuma; T R Shearer
Journal:  Surv Ophthalmol       Date:  2008 Mar-Apr       Impact factor: 6.048

2.  Genomic organization of mouse Capn5 and Capn6 genes confirms that they are a distinct calpain subfamily.

Authors:  K Matena; T Boehm; N Dear
Journal:  Genomics       Date:  1998-02-15       Impact factor: 5.736

3.  Intravitreal injection or topical eye-drop application of a μ-calpain C2L domain peptide protects against photoreceptor cell death in Royal College of Surgeons' rats, a model of retinitis pigmentosa.

Authors:  Taku Ozaki; Mitsuru Nakazawa; Tetsuro Yamashita; Hiroyuki Sorimachi; Shoji Hata; Hiroshi Tomita; Hitomi Isago; Ayaka Baba; Sei-Ichi Ishiguro
Journal:  Biochim Biophys Acta       Date:  2012-08-03

4.  CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa.

Authors:  Wen-Hsuan Wu; Yi-Ting Tsai; Sally Justus; Ting-Ting Lee; Lijuan Zhang; Chyuan-Sheng Lin; Alexander G Bassuk; Vinit B Mahajan; Stephen H Tsang
Journal:  Mol Ther       Date:  2016-05-20       Impact factor: 11.454

5.  Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

Authors:  E M Stone; A E Kimura; J C Folk; S R Bennett; B E Nichols; L M Streb; V C Sheffield
Journal:  Hum Mol Genet       Date:  1992-12       Impact factor: 6.150

6.  Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration.

Authors:  Vinit B Mahajan; Jessica M Skeie; Alexander G Bassuk; John H Fingert; Terry A Braun; Heather T Daggett; James C Folk; Val C Sheffield; Edwin M Stone
Journal:  PLoS Genet       Date:  2012-10-04       Impact factor: 5.917

7.  Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy.

Authors:  Hannah A Rowell; Alexander G Bassuk; Vinit B Mahajan
Journal:  Clin Ophthalmol       Date:  2012-12-06

8.  Structural modeling of a novel CAPN5 mutation that causes uveitis and neovascular retinal detachment.

Authors:  Alexander G Bassuk; Steven Yeh; Shu Wu; Daniel F Martin; Stephen H Tsang; Lokesh Gakhar; Vinit B Mahajan
Journal:  PLoS One       Date:  2015-04-09       Impact factor: 3.240

Review 9.  CRISPR-Cas Genome Surgery in Ophthalmology.

Authors:  James E DiCarlo; Jesse D Sengillo; Sally Justus; Thiago Cabral; Stephen H Tsang; Vinit B Mahajan
Journal:  Transl Vis Sci Technol       Date:  2017-05-31       Impact factor: 3.283

10.  Precision Medicine: Genetic Repair of Retinitis Pigmentosa in Patient-Derived Stem Cells.

Authors:  Alexander G Bassuk; Andrew Zheng; Yao Li; Stephen H Tsang; Vinit B Mahajan
Journal:  Sci Rep       Date:  2016-01-27       Impact factor: 4.379

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  4 in total

1.  Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy.

Authors:  Gabriel Velez; Jing Yang; Angela S Li; Stephen H Tsang; Alexander G Bassuk; Vinit B Mahajan
Journal:  Sci Rep       Date:  2019-05-20       Impact factor: 4.379

2.  Phenotypic variance in Calpain-5 retinal degeneration.

Authors:  Peter H Tang; Teja Chemudupati; Katherine J Wert; James C Folk; MaryAnn Mahajan; Stephen H Tsang; Alexander G Bassuk; Vinit B Mahajan
Journal:  Am J Ophthalmol Case Rep       Date:  2020-02-24

Review 3.  Molecular Surgery: Proteomics of a Rare Genetic Disease Gives Insight into Common Causes of Blindness.

Authors:  Gabriel Velez; Vinit B Mahajan
Journal:  iScience       Date:  2020-10-13

4.  Long-Term Outcomes and Risk Factors for Severe Vision Loss in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy (ADNIV).

Authors:  Timothy M Boyce; S Scott Whitmore; Katayoun Varzavand; Stephen R Russell; Elliott H Sohn; James C Folk; Edwin M Stone; Ian C Han
Journal:  Am J Ophthalmol       Date:  2021-07-21       Impact factor: 5.488

  4 in total

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