Literature DB >> 30927187

Two-color pupillometry in KCNV2 retinopathy.

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

Abstract

PURPOSE: To investigate receptor and post-receptor function in KCNV2 retinopathy [cone dystrophy with supernormal rod electroretinogram (ERG)], using the pupillary light reflex (PLR) and the ERG.
METHODS: Two unrelated patients (1 male and 1 female) with molecularly confirmed KCNV2 retinopathy underwent full-field two-color pupillometry testing in one eye, with monitoring of the stimulated eye by an infrared digital camera. Pupillometry stimuli consisted of 1-s duration, short-wavelength (465-nm, blue) and long-wavelength (642-nm, red) stimuli. Pupillometry intensity series were performed under both a dark-adapted condition and a light-adapted condition (on a 0.76-log cd m-2 blue background). The transient PLR, defined as the maximum constriction following flash onset, was measured under all conditions. The melanopsin-mediated sustained constriction was measured 5-7 s following flash offset for the highest flash luminance presented in the dark. Both patients were also tested in one eye with the full-field ERG, including a dark-adapted intensity series and ISCEV standard stimuli.
RESULTS: Dark-adapted PLRs were markedly attenuated or extinguished for low-luminance stimuli, but the responses to higher-luminance blue stimuli were within normal limits. Light-adapted PLRs to blue stimuli were generally within normal limits, exceeding the responses to photopically matched red stimuli. Thus, light-adapted responses were consistent with either rod or S-cone mediation of the PLR. Melanopsin-mediated sustained PLRs were within normal limits. ERG showed the characteristic findings previously reported in this condition. Cone-mediated ERG responses were markedly decreased in amplitude. Rod-mediated ERG responses were absent for low-luminance stimuli (- 3 log cd s m-2), but had normal amplitude for stimuli of - 2 log cd s m-2 and above (although none were "supernormal"). The b-wave for the dark-adapted ISCEV standard - 2 log cd s m-2 stimulus was markedly delayed, whereas the b-wave timing was generally normal for higher flash luminances.
CONCLUSIONS: The abnormalities measured by pupillometry have a similar pattern to the outer-retinal abnormalities measured by ERG in KCNV2 retinopathy. These findings as well as the normal sustained PLR suggest that inner-retinal function may be preserved in KCNV2 retinopathy and highlight the potential for therapies designed to restore outer-retinal function in these individuals.

Entities:  

Keywords:  Cone dystrophy with supernormal rod ERG; KCNV2; KCNV2 retinopathy; Pupillary light reflex; Pupillometry

Mesh:

Substances:

Year:  2019        PMID: 30927187      PMCID: PMC6625896          DOI: 10.1007/s10633-019-09691-w

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


  25 in total

1.  A detailed phenotypic study of "cone dystrophy with supernormal rod ERG".

Authors:  M Michaelides; G E Holder; A R Webster; D M Hunt; A C Bird; F W Fitzke; J D Mollon; A T Moore
Journal:  Br J Ophthalmol       Date:  2005-03       Impact factor: 4.638

2.  Sites of disease action in a retinal dystrophy with supernormal and delayed rod electroretinogram b-waves.

Authors:  D C Hood; A V Cideciyan; D A Halevy; S G Jacobson
Journal:  Vision Res       Date:  1996-03       Impact factor: 1.886

3.  High-resolution optical coherence tomography imaging in KCNV2 retinopathy.

Authors:  Panagiotis I Sergouniotis; Graham E Holder; Anthony G Robson; Michel Michaelides; Andrew R Webster; Anthony T Moore
Journal:  Br J Ophthalmol       Date:  2011-05-10       Impact factor: 4.638

4.  ISCEV Standard for full-field clinical electroretinography (2015 update).

Authors:  Daphne L McCulloch; Michael F Marmor; Mitchell G Brigell; Ruth Hamilton; Graham E Holder; Radouil Tzekov; Michael Bach
Journal:  Doc Ophthalmol       Date:  2014-12-14       Impact factor: 2.379

5.  Toward a clinical protocol for assessing rod, cone, and melanopsin contributions to the human pupil response.

Authors:  Jason C Park; Ana L Moura; Ali S Raza; David W Rhee; Randy H Kardon; Donald C Hood
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-08-22       Impact factor: 4.799

6.  "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.

Authors:  Anthony G Robson; Andrew R Webster; Michel Michaelides; Susan M Downes; Jill A Cowing; David M Hunt; Anthony T Moore; Graham E Holder
Journal:  Retina       Date:  2010-01       Impact factor: 4.256

7.  Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

Authors:  Bernd Wissinger; Susann Dangel; Herbert Jägle; Lars Hansen; Britta Baumann; Günther Rudolph; Christiane Wolf; Michael Bonin; Katja Koeppen; Thomas Ladewig; Susanne Kohl; Eberhart Zrenner; Thomas Rosenberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-02       Impact factor: 4.799

8.  Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes.

Authors:  Gábor Czirják; Zsuzsanna E Tóth; Péter Enyedi
Journal:  J Neurophysiol       Date:  2007-07-25       Impact factor: 2.714

9.  Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod function.

Authors:  Andrew Stockman; G Bruce Henning; Michel Michaelides; Anthony T Moore; Andrew R Webster; Jocelyn Cammack; Caterina Ripamonti
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-02-10       Impact factor: 4.799

10.  Rod and cone function in patients with KCNV2 retinopathy.

Authors:  Ditta Zobor; Susanne Kohl; Bernd Wissinger; Eberhart Zrenner; Herbert Jägle
Journal:  PLoS One       Date:  2012-10-15       Impact factor: 3.240

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  6 in total

1.  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

2.  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

3.  Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy.

Authors:  Frederick T Collison; Gerald A Fishman; Takayuki Nagasaki; Jana Zernant; J Jason McAnany; Jason C Park; Rando Allikmets
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-05-01       Impact factor: 4.799

Review 4.  KCNV2 retinopathy: clinical features, molecular genetics and directions for future therapy.

Authors:  Thales A C De Guimaraes; Michalis Georgiou; Anthony G Robson; Michel Michaelides
Journal:  Ophthalmic Genet       Date:  2020-05-22       Impact factor: 1.803

5.  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

6.  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

  6 in total

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