Literature DB >> 27033713

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

Frederick T Collison1, Jason C Park2, Gerald A Fishman3,4, Edwin M Stone5, J Jason McAnany2.   

Abstract

PURPOSE: The purpose of this study was to evaluate pupillary light reflexes (PLRs) mediated by rod, cone, and intrinsically photosensitive retinal ganglion cell pathways as indices of outer- and inner-retinal function in patients who have enhanced S-cone syndrome (ESCS) due to NR2E3 mutations.
METHODS: Four patients with ESCS (ages 16-23 years) participated in the study. Subjects were tested with long- and short-wavelength single-flash full-field ERG stimuli under light-adapted conditions. They were also tested with an established pupillometry protocol involving 1-s duration, long- and short-wavelength stimuli under dark- and light-adapted conditions. The PLR was measured as a function of stimulus luminance. Transient PLRs were measured under all conditions, and sustained PLRs were measured under the highest luminance dark-adapted condition.
RESULTS: Two-color light-adapted full-field ERGs demonstrated larger amplitude responses for short-wavelength stimuli relative to long-wavelength stimuli of the same photopic luminance, with three of four ESCS patients having super-normal a-wave amplitudes to the short-wavelength stimulus. b/a wave ratios were reduced in all four cases. Transient PLRs elicited by low-luminance stimuli under dark-adapted conditions (rod-mediated) were unrecordable, whereas the sustained PLRs elicited by high-luminance stimuli (melanopsin-mediated) were normal. Cone-mediated PLRs were recordable for all four patients, but generally lower than normal in amplitude. However, the cone-mediated PLR was larger for the short-wavelength stimulus compared to the photopically matched long-wavelength stimulus at high luminances, a pattern that was not observed for control subjects. None of the PLR conditions demonstrated "super-normal" responses.
CONCLUSION: ESCS patients appear to have generally well-preserved cone- and melanopsin-mediated PLRs, indicating intact inner-retinal function. Two-color pupillometry demonstrates greater sensitivity to short-wavelength light under higher-luminance conditions and could complement the ERG as a tool for evaluating retinal function in ESCS.

Entities:  

Keywords:  Enhanced S-cone syndrome; Full-field electroretinogram; NR2E3; Pupillary light reflex; Pupillometry

Mesh:

Substances:

Year:  2016        PMID: 27033713      PMCID: PMC6088747          DOI: 10.1007/s10633-016-9535-0

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  33 in total

1.  Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors.

Authors:  Hong Cheng; Naheed W Khan; Jerome E Roger; Anand Swaroop
Journal:  Hum Mol Genet       Date:  2011-08-03       Impact factor: 6.150

2.  Opponent melanopsin and S-cone signals in the human pupillary light response.

Authors:  Manuel Spitschan; Sandeep Jain; David H Brainard; Geoffrey K Aguirre
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-13       Impact factor: 11.205

3.  Test-retest reliability of hemifield, central-field, and full-field chromatic pupillometry for assessing the function of melanopsin-containing retinal ganglion cells.

Authors:  Shaobo Lei; Herbert C Goltz; Manokaraananthan Chandrakumar; Agnes M F Wong
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-01-27       Impact factor: 4.799

4.  S-cone contribution to pupillary responses evoked by chromatic flash offset.

Authors:  E Kimura; R S Young
Journal:  Vision Res       Date:  1999-03       Impact factor: 1.886

5.  Efficacy of topical dorzolamide for treatment of cystic macular lesions in a patient with enhanced S-cone syndrome.

Authors:  Mohamed A Genead; Gerald A Fishman; J Jason McAnany
Journal:  Doc Ophthalmol       Date:  2010-09-15       Impact factor: 2.379

6.  The enhanced S cone syndrome: an analysis of receptoral and post-receptoral changes.

Authors:  V C Greenstein; Q Zaidi; D C Hood; B Spehar; A V Cideciyan; S G Jacobson
Journal:  Vision Res       Date:  1996-11       Impact factor: 1.886

7.  Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations.

Authors:  Catherine Cassiman; Werner Spileers; Elfride De Baere; Thomy de Ravel; Ingele Casteels
Journal:  Ophthalmic Genet       Date:  2012-10-05       Impact factor: 1.803

Review 8.  Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction.

Authors:  Neena B Haider; Nissa Mollema; Meghan Gaule; Yang Yuan; Andrew J Sachs; Arne M Nystuen; Jürgen K Naggert; Patsy M Nishina
Journal:  Exp Eye Res       Date:  2009-04-18       Impact factor: 3.467

9.  Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity.

Authors:  M F Marmor; S G Jacobson; M H Foerster; U Kellner; R G Weleber
Journal:  Am J Ophthalmol       Date:  1990-08-15       Impact factor: 5.258

10.  A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3.

Authors:  Atsuhiro Kanda; Anand Swaroop
Journal:  Mol Vis       Date:  2009-10-24       Impact factor: 2.367

View more
  9 in total

1.  Reply: Pupil area and photopigment spectral sensitivity are relevant to study of migraine photophobia.

Authors:  Rami Burstein
Journal:  Brain       Date:  2016-11-15       Impact factor: 13.501

2.  Cone pathway dysfunction in Jalili syndrome due to a novel familial variant of CNNM4 revealed by pupillometry and electrophysiologic investigations.

Authors:  Robert A Hyde; Evelina Kratunova; Jason C Park; J Jason McAnany
Journal:  Ophthalmic Genet       Date:  2021-12-07       Impact factor: 1.274

3.  Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function.

Authors:  Arun K Krishnan; Samuel G Jacobson; Alejandro J Roman; Bhavya S Iyer; Alexandra V Garafalo; Elise Héon; Artur V Cideciyan
Journal:  Vision Res       Date:  2020-02-20       Impact factor: 1.886

4.  Pupillary responses in non-proliferative diabetic retinopathy.

Authors:  Jason C Park; Yi-Fan Chen; Norman P Blair; Felix Y Chau; Jennifer I Lim; Yannek I Leiderman; Mahnaz Shahidi; J Jason McAnany
Journal:  Sci Rep       Date:  2017-03-23       Impact factor: 4.379

5.  iPhone-based Pupillometry: A Novel Approach for Assessing the Pupillary Light Reflex.

Authors:  J Jason McAnany; Brandon M Smith; Amy Garland; Steven L Kagen
Journal:  Optom Vis Sci       Date:  2018-10       Impact factor: 1.973

6.  Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis.

Authors:  J Jason McAnany; Jason C Park; Gerald A Fishman; Frederick T Collison
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-06-03       Impact factor: 4.799

7.  Pupillary reflex and behavioral masking responses to light as functional measures of retinal degeneration in mice.

Authors:  Ethan O Contreras; Carley G Dearing; Crystal A Ashinhurst; Betty A Fish; Sajila N Hossain; Ariana M Rey; Primal D Silva; Stewart Thompson
Journal:  PLoS One       Date:  2021-01-25       Impact factor: 3.240

8.  Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients.

Authors:  Saoud Al-Khuzaei; Suzanne Broadgate; Stephanie Halford; Jasleen K Jolly; Morag Shanks; Penny Clouston; Susan M Downes
Journal:  Genes (Basel)       Date:  2020-10-29       Impact factor: 4.096

9.  Electrophysiological and Pupillometric Abnormalities in PROM1 Cone-Rod Dystrophy.

Authors:  Jason C Park; Frederick T Collison; Gerald A Fishman; J Jason McAnany
Journal:  Transl Vis Sci Technol       Date:  2020-08-17       Impact factor: 3.283

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.