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Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy

Carriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus...

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Autores principales: Rossi, Ethan A., Achtman, Rebecca L., Guidon, Arnaud, Williams, David R., Roorda, Austin, Bavelier, Daphne, Carroll, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585243/
https://www.ncbi.nlm.nih.gov/pubmed/23469117
http://dx.doi.org/10.1371/journal.pone.0057956
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author Rossi, Ethan A.
Achtman, Rebecca L.
Guidon, Arnaud
Williams, David R.
Roorda, Austin
Bavelier, Daphne
Carroll, Joseph
author_facet Rossi, Ethan A.
Achtman, Rebecca L.
Guidon, Arnaud
Williams, David R.
Roorda, Austin
Bavelier, Daphne
Carroll, Joseph
author_sort Rossi, Ethan A.
collection PubMed
description Carriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus of fixation and visual resolution was tested at two eccentric locations (2.5° and 8°) with spectacle correction only. Adaptive optics corrected resolution acuity and cone spacing were simultaneously measured at several locations within the central fovea with adaptive optics scanning laser ophthalmoscopy (AOSLO). Fixation stability was assessed by extracting eye motion data from AOSLO videos. Retinotopic mapping using fMRI was carried out to estimate the area of early cortical regions, including that of the foveal confluence. Without adaptive optics correction, BCM carriers appeared to have normal visual function, with normal contrast sensitivity and visual resolution, but with AO-correction, visual resolution was significantly worse than normal. This resolution deficit is not explained by cone loss alone and is suggestive of an associated loss of retinal ganglion cells. However, despite evidence suggesting a reduction in the number of retinal ganglion cells, retinotopic mapping showed no reduction in the cortical area of the foveal confluence. These results suggest that ganglion cell density may not govern the foveal overrepresentation in the cortex. We propose that it is not the number of afferents, but rather the content of the information relayed to the cortex from the retina across the visual field that governs cortical magnification, as under normal viewing conditions this information is similar in both BCM carriers and normal controls.
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spelling pubmed-35852432013-03-06 Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy Rossi, Ethan A. Achtman, Rebecca L. Guidon, Arnaud Williams, David R. Roorda, Austin Bavelier, Daphne Carroll, Joseph PLoS One Research Article Carriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus of fixation and visual resolution was tested at two eccentric locations (2.5° and 8°) with spectacle correction only. Adaptive optics corrected resolution acuity and cone spacing were simultaneously measured at several locations within the central fovea with adaptive optics scanning laser ophthalmoscopy (AOSLO). Fixation stability was assessed by extracting eye motion data from AOSLO videos. Retinotopic mapping using fMRI was carried out to estimate the area of early cortical regions, including that of the foveal confluence. Without adaptive optics correction, BCM carriers appeared to have normal visual function, with normal contrast sensitivity and visual resolution, but with AO-correction, visual resolution was significantly worse than normal. This resolution deficit is not explained by cone loss alone and is suggestive of an associated loss of retinal ganglion cells. However, despite evidence suggesting a reduction in the number of retinal ganglion cells, retinotopic mapping showed no reduction in the cortical area of the foveal confluence. These results suggest that ganglion cell density may not govern the foveal overrepresentation in the cortex. We propose that it is not the number of afferents, but rather the content of the information relayed to the cortex from the retina across the visual field that governs cortical magnification, as under normal viewing conditions this information is similar in both BCM carriers and normal controls. Public Library of Science 2013-02-28 /pmc/articles/PMC3585243/ /pubmed/23469117 http://dx.doi.org/10.1371/journal.pone.0057956 Text en © 2013 Rossi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rossi, Ethan A.
Achtman, Rebecca L.
Guidon, Arnaud
Williams, David R.
Roorda, Austin
Bavelier, Daphne
Carroll, Joseph
Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title_full Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title_fullStr Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title_full_unstemmed Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title_short Visual Function and Cortical Organization in Carriers of Blue Cone Monochromacy
title_sort visual function and cortical organization in carriers of blue cone monochromacy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585243/
https://www.ncbi.nlm.nih.gov/pubmed/23469117
http://dx.doi.org/10.1371/journal.pone.0057956
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