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Prediction of glaucoma severity using parameters from the electroretinogram

Glaucoma is an optic neuropathy that results in the progressive loss of retinal ganglion cells (RGCs), which are known to exhibit functional changes prior to cell loss. The electroretinogram (ERG) is a method that enables an objective assessment of retinal function, and the photopic negative respons...

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Autores principales: Sarossy, Marc, Crowston, Jonathan, Kumar, Dinesh, Weymouth, Anne, Wu, Zhichao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668922/
https://www.ncbi.nlm.nih.gov/pubmed/34903831
http://dx.doi.org/10.1038/s41598-021-03421-6
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author Sarossy, Marc
Crowston, Jonathan
Kumar, Dinesh
Weymouth, Anne
Wu, Zhichao
author_facet Sarossy, Marc
Crowston, Jonathan
Kumar, Dinesh
Weymouth, Anne
Wu, Zhichao
author_sort Sarossy, Marc
collection PubMed
description Glaucoma is an optic neuropathy that results in the progressive loss of retinal ganglion cells (RGCs), which are known to exhibit functional changes prior to cell loss. The electroretinogram (ERG) is a method that enables an objective assessment of retinal function, and the photopic negative response (PhNR) has conventionally been used to provide a measure of RGC function. This study sought to examine if additional parameters from the ERG (amplitudes of the a-, b-, i-wave, as well the trough between the b- and i-wave), a multivariate adaptive regression splines (MARS; a non-linear) model and achromatic stimuli could better predict glaucoma severity in 103 eyes of 55 individuals with glaucoma. Glaucoma severity was determined using standard automated perimetry and optical coherence tomography imaging. ERGs targeting the PhNR were recorded with a chromatic (red-on-blue) and achromatic (white-on-white) stimulus with the same luminance. Linear and MARS models were fitted to predict glaucoma severity using the PhNR only or all ERG markers, derived from chromatic and achromatic stimuli. Use of all ERG markers predicted glaucoma severity significantly better than the PhNR alone (P ≤ 0.02), and the MARS performed better than linear models when using all markers (P = 0.01), but there was no significant difference between the achromatic and chromatic stimulus models. This study shows that there is more information present in the photopic ERG beyond the conventional PhNR measure in characterizing RGC function.
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spelling pubmed-86689222021-12-15 Prediction of glaucoma severity using parameters from the electroretinogram Sarossy, Marc Crowston, Jonathan Kumar, Dinesh Weymouth, Anne Wu, Zhichao Sci Rep Article Glaucoma is an optic neuropathy that results in the progressive loss of retinal ganglion cells (RGCs), which are known to exhibit functional changes prior to cell loss. The electroretinogram (ERG) is a method that enables an objective assessment of retinal function, and the photopic negative response (PhNR) has conventionally been used to provide a measure of RGC function. This study sought to examine if additional parameters from the ERG (amplitudes of the a-, b-, i-wave, as well the trough between the b- and i-wave), a multivariate adaptive regression splines (MARS; a non-linear) model and achromatic stimuli could better predict glaucoma severity in 103 eyes of 55 individuals with glaucoma. Glaucoma severity was determined using standard automated perimetry and optical coherence tomography imaging. ERGs targeting the PhNR were recorded with a chromatic (red-on-blue) and achromatic (white-on-white) stimulus with the same luminance. Linear and MARS models were fitted to predict glaucoma severity using the PhNR only or all ERG markers, derived from chromatic and achromatic stimuli. Use of all ERG markers predicted glaucoma severity significantly better than the PhNR alone (P ≤ 0.02), and the MARS performed better than linear models when using all markers (P = 0.01), but there was no significant difference between the achromatic and chromatic stimulus models. This study shows that there is more information present in the photopic ERG beyond the conventional PhNR measure in characterizing RGC function. Nature Publishing Group UK 2021-12-13 /pmc/articles/PMC8668922/ /pubmed/34903831 http://dx.doi.org/10.1038/s41598-021-03421-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sarossy, Marc
Crowston, Jonathan
Kumar, Dinesh
Weymouth, Anne
Wu, Zhichao
Prediction of glaucoma severity using parameters from the electroretinogram
title Prediction of glaucoma severity using parameters from the electroretinogram
title_full Prediction of glaucoma severity using parameters from the electroretinogram
title_fullStr Prediction of glaucoma severity using parameters from the electroretinogram
title_full_unstemmed Prediction of glaucoma severity using parameters from the electroretinogram
title_short Prediction of glaucoma severity using parameters from the electroretinogram
title_sort prediction of glaucoma severity using parameters from the electroretinogram
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668922/
https://www.ncbi.nlm.nih.gov/pubmed/34903831
http://dx.doi.org/10.1038/s41598-021-03421-6
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