Literature DB >> 23049087

Phosphene thresholds elicited by transcorneal electrical stimulation in healthy subjects and patients with retinal diseases.

Lubka Naycheva1, Andreas Schatz, Tobias Röck, Gabriel Willmann, André Messias, Karl Ulrich Bartz-Schmidt, Eberhart Zrenner, Florian Gekeler.   

Abstract

PURPOSE: To evaluate electrically evoked phosphene thresholds (EPTs) in healthy subjects and in patients with retinal disease and to assess repeatability and possible correlations with common ophthalmologic tests.
METHODS: In all, 117 individuals participated: healthy subjects (n = 20) and patients with retinitis pigmentosa (RP, n = 30), Stargardt's disease (STG, n = 14), retinal artery occlusion (RAO, n = 20), nonarteritic anterior ischemic optic neuropathy (NAION, n = 16), and primary open-angle glaucoma (POAG, n = 17). EPTs were determined at 3, 6, 9, 20, 40, 60, and 80 Hz with 5 + 5-ms biphasic current pulses using DTL electrodes. Subjects were examined twice (test-retest range: 1-6 weeks). An empirical model was developed to describe the current-frequency relationship of EPTs. Visual acuity, visual field (kinetic + static), electrophysiology (RP, RAO, STG: Ganzfeld-electroretinography [ERG]/multifocal-ERG; POAG: pattern-ERG; NAION: VEP), slit-lamp biomicroscopy, fundus examination, and tonometry were assessed.
RESULTS: EPTS varied between disease groups (20 HZ: healthy subjects: 0.062 ± 0.038 mA; STG: 0.102 ± 0.097 mA; POAG: 0.127 ± 0.09 mA; NAION: 0.244 ± 0.126 mA; RP: 0.371 ± 0.223 mA; RAO: 0.988 ± 1.142 mA). In all groups EPTs were lowest at 20 Hz. In patients with retinal diseases and across all frequencies EPTs were significantly higher than those in healthy subjects, except in STG at 20 Hz (P = 0.09) and 40 Hz (P = 0.17). Test-retest difference at 20 Hz was 0.006 mA in the healthy group and 0.003-0.04 mA in disease groups.
CONCLUSIONS: Considering the fast, safe, and reliable practicability of EPT testing, this test might be used more often under clinical circumstances. Determination of EPTs could be potentially useful in elucidation of the progress of ophthalmologic diseases, either in addition to standard clinical assessment or under conditions in which these standard tests cannot be used meaningfully. (ClinicalTrials.gov number, NCT00804102.).

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Mesh:

Year:  2012        PMID: 23049087     DOI: 10.1167/iovs.12-9612

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


  16 in total

1.  Temporal properties of network-mediated responses to repetitive stimuli are dependent upon retinal ganglion cell type.

Authors:  Maesoon Im; Shelley I Fried
Journal:  J Neural Eng       Date:  2016-02-23       Impact factor: 5.379

2.  Indirect activation elicits strong correlations between light and electrical responses in ON but not OFF retinal ganglion cells.

Authors:  Maesoon Im; Shelley I Fried
Journal:  J Physiol       Date:  2015-06-30       Impact factor: 5.182

Review 3.  Transcranial electrical stimulation nomenclature.

Authors:  Marom Bikson; Zeinab Esmaeilpour; Devin Adair; Greg Kronberg; William J Tyler; Andrea Antal; Abhishek Datta; Bernhard A Sabel; Michael A Nitsche; Colleen Loo; Dylan Edwards; Hamed Ekhtiari; Helena Knotkova; Adam J Woods; Benjamin M Hampstead; Bashar W Badran; Angel V Peterchev
Journal:  Brain Stimul       Date:  2019-07-17       Impact factor: 8.955

4.  Randomized controlled trial of electro-stimulation therapies to modulate retinal blood flow and visual function in retinitis pigmentosa.

Authors:  Ava K Bittner; Kenneth Seger; Rachel Salveson; Samantha Kayser; Natalia Morrison; Patricia Vargas; Deborah Mendelsohn; Jorge Han; Hua Bi; Gislin Dagnelie; Alexandra Benavente; Jessica Ramella-Roman
Journal:  Acta Ophthalmol       Date:  2017-11-11       Impact factor: 3.761

Review 5.  Electrical Stimulation as a Means for Improving Vision.

Authors:  Amer Sehic; Shuai Guo; Kin-Sang Cho; Rima M Corraya; Dong F Chen; Tor P Utheim
Journal:  Am J Pathol       Date:  2016-11       Impact factor: 4.307

6.  Longevity of visual improvements following transcorneal electrical stimulation and efficacy of retreatment in three individuals with retinitis pigmentosa.

Authors:  Ava K Bittner; Kenneth Seger
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2017-12-08       Impact factor: 3.117

Review 7.  Electrical stimulation of cranial nerves in cognition and disease.

Authors:  Devin Adair; Dennis Truong; Zeinab Esmaeilpour; Nigel Gebodh; Helen Borges; Libby Ho; J Douglas Bremner; Bashar W Badran; Vitaly Napadow; Vincent P Clark; Marom Bikson
Journal:  Brain Stimul       Date:  2020-02-23       Impact factor: 8.955

8.  [Transcorneal electrical stimulation in primary open angle glaucoma].

Authors:  T Röck; L Naycheva; G Willmann; B Wilhelm; T Peters; E Zrenner; K U Bartz-Schmidt; F Gekeler; A Schatz
Journal:  Ophthalmologe       Date:  2017-10       Impact factor: 1.059

9.  Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapy.

Authors:  Samantha R De Silva; Alun R Barnard; Steven Hughes; Shu K E Tam; Chris Martin; Mandeep S Singh; Alona O Barnea-Cramer; Michelle E McClements; Matthew J During; Stuart N Peirson; Mark W Hankins; Robert E MacLaren
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-02       Impact factor: 11.205

10.  Electric stimulus duration alters network-mediated responses depending on retinal ganglion cell type.

Authors:  Maesoon Im; Paul Werginz; Shelley I Fried
Journal:  J Neural Eng       Date:  2018-02-08       Impact factor: 5.379

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