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Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies

The goal of neuroprotection in optic neuropathies is to prevent loss of retinal ganglion cells (RGCs) and spare their function. The ideal time window for initiating neuroprotective treatments should be the preclinical period at which RGCs start losing their functional integrity before dying. Noninva...

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Autores principales: Porciatti, Vittorio, Chou, Tsung-Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145583/
https://www.ncbi.nlm.nih.gov/pubmed/35628564
http://dx.doi.org/10.3390/ijms23105751
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author Porciatti, Vittorio
Chou, Tsung-Han
author_facet Porciatti, Vittorio
Chou, Tsung-Han
author_sort Porciatti, Vittorio
collection PubMed
description The goal of neuroprotection in optic neuropathies is to prevent loss of retinal ganglion cells (RGCs) and spare their function. The ideal time window for initiating neuroprotective treatments should be the preclinical period at which RGCs start losing their functional integrity before dying. Noninvasive electrophysiological tests such as the Pattern Electroretinogram (PERG) can assess the ability of RGCs to generate electrical signals under a protracted degenerative process in both clinical conditions and experimental models, which may have both diagnostic and prognostic values and provide the rationale for early treatment. The PERG can be used to longitudinally monitor the acute and chronic effects of neuroprotective treatments. User-friendly versions of the PERG technology are now commercially available for both clinical and experimental use.
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spelling pubmed-91455832022-05-29 Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies Porciatti, Vittorio Chou, Tsung-Han Int J Mol Sci Perspective The goal of neuroprotection in optic neuropathies is to prevent loss of retinal ganglion cells (RGCs) and spare their function. The ideal time window for initiating neuroprotective treatments should be the preclinical period at which RGCs start losing their functional integrity before dying. Noninvasive electrophysiological tests such as the Pattern Electroretinogram (PERG) can assess the ability of RGCs to generate electrical signals under a protracted degenerative process in both clinical conditions and experimental models, which may have both diagnostic and prognostic values and provide the rationale for early treatment. The PERG can be used to longitudinally monitor the acute and chronic effects of neuroprotective treatments. User-friendly versions of the PERG technology are now commercially available for both clinical and experimental use. MDPI 2022-05-20 /pmc/articles/PMC9145583/ /pubmed/35628564 http://dx.doi.org/10.3390/ijms23105751 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Perspective
Porciatti, Vittorio
Chou, Tsung-Han
Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title_full Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title_fullStr Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title_full_unstemmed Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title_short Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies
title_sort using noninvasive electrophysiology to determine time windows of neuroprotection in optic neuropathies
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145583/
https://www.ncbi.nlm.nih.gov/pubmed/35628564
http://dx.doi.org/10.3390/ijms23105751
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