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Contrast Increment and Decrement Processing in Individuals With and Without Diabetes
PURPOSE: Animal models suggest that ON retinal ganglion cells (RGCs) may be more vulnerable to diabetic insult than OFF cells. Using three psychophysical tasks to infer the function of ON and OFF RGCs, we hypothesized that functional responses to contrast increments will be preferentially affected i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132322/ https://www.ncbi.nlm.nih.gov/pubmed/37083950 http://dx.doi.org/10.1167/iovs.64.4.26 |
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author | Tang, Vanessa Thien Sze Symons, Robert Charles Andrew Fourlanos, Spiros Guest, Daryl McKendrick, Allison Maree |
author_facet | Tang, Vanessa Thien Sze Symons, Robert Charles Andrew Fourlanos, Spiros Guest, Daryl McKendrick, Allison Maree |
author_sort | Tang, Vanessa Thien Sze |
collection | PubMed |
description | PURPOSE: Animal models suggest that ON retinal ganglion cells (RGCs) may be more vulnerable to diabetic insult than OFF cells. Using three psychophysical tasks to infer the function of ON and OFF RGCs, we hypothesized that functional responses to contrast increments will be preferentially affected in early diabetes mellitus (DM) compared to contrast decrement responses. METHODS: Fifty-two people with DM (type 1 or type 2) (mean age = 34.8 years, range = 18–60 years) and 48 age-matched controls (mean age = 35.4 years, range = 18–60 years) participated. Experiment 1 measured contrast sensitivity to increments and decrements at four visual field locations. Experiments 2 and 3 measured visual temporal processing using (i) a response time (RT) task, and (ii) a temporal order judgment task. Mean RT and accuracy were collected for experiment 2, whereas experiment 3 measured temporal thresholds. RESULTS: For experiment 1, the DM group showed reduced increment and decrement contrast sensitivity (F (1, 97) = 4.04, P = 0.047) especially for the central location. For experiment 2, those with DM demonstrated slower RT and lower response accuracies to increments and decrements (increments: U = 780, P = 0.01, decrements: U = 749, P = 0.005). For experiment 3, performance was similar between groups (F (1, 91) = 2.52, P = 0.137). CONCLUSIONS: When assessed cross-sectionally, nonselective functional consequences of retinal neuron damage are present in early DM, particularly for foveal testing. Whether increment-decrement functional indices relate to diabetic retinopathy (DR) progression or poorer visual prognosis in DM requires further study. |
format | Online Article Text |
id | pubmed-10132322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101323222023-04-27 Contrast Increment and Decrement Processing in Individuals With and Without Diabetes Tang, Vanessa Thien Sze Symons, Robert Charles Andrew Fourlanos, Spiros Guest, Daryl McKendrick, Allison Maree Invest Ophthalmol Vis Sci Clinical and Epidemiologic Research PURPOSE: Animal models suggest that ON retinal ganglion cells (RGCs) may be more vulnerable to diabetic insult than OFF cells. Using three psychophysical tasks to infer the function of ON and OFF RGCs, we hypothesized that functional responses to contrast increments will be preferentially affected in early diabetes mellitus (DM) compared to contrast decrement responses. METHODS: Fifty-two people with DM (type 1 or type 2) (mean age = 34.8 years, range = 18–60 years) and 48 age-matched controls (mean age = 35.4 years, range = 18–60 years) participated. Experiment 1 measured contrast sensitivity to increments and decrements at four visual field locations. Experiments 2 and 3 measured visual temporal processing using (i) a response time (RT) task, and (ii) a temporal order judgment task. Mean RT and accuracy were collected for experiment 2, whereas experiment 3 measured temporal thresholds. RESULTS: For experiment 1, the DM group showed reduced increment and decrement contrast sensitivity (F (1, 97) = 4.04, P = 0.047) especially for the central location. For experiment 2, those with DM demonstrated slower RT and lower response accuracies to increments and decrements (increments: U = 780, P = 0.01, decrements: U = 749, P = 0.005). For experiment 3, performance was similar between groups (F (1, 91) = 2.52, P = 0.137). CONCLUSIONS: When assessed cross-sectionally, nonselective functional consequences of retinal neuron damage are present in early DM, particularly for foveal testing. Whether increment-decrement functional indices relate to diabetic retinopathy (DR) progression or poorer visual prognosis in DM requires further study. The Association for Research in Vision and Ophthalmology 2023-04-21 /pmc/articles/PMC10132322/ /pubmed/37083950 http://dx.doi.org/10.1167/iovs.64.4.26 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Clinical and Epidemiologic Research Tang, Vanessa Thien Sze Symons, Robert Charles Andrew Fourlanos, Spiros Guest, Daryl McKendrick, Allison Maree Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title | Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title_full | Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title_fullStr | Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title_full_unstemmed | Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title_short | Contrast Increment and Decrement Processing in Individuals With and Without Diabetes |
title_sort | contrast increment and decrement processing in individuals with and without diabetes |
topic | Clinical and Epidemiologic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132322/ https://www.ncbi.nlm.nih.gov/pubmed/37083950 http://dx.doi.org/10.1167/iovs.64.4.26 |
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