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Sensitivity to S-Cone Stimuli and the Development of Myopia
PURPOSE: Longitudinal chromatic aberration (LCA) is a color signal available to the emmetropization process that causes greater myopic defocus of short wavelengths than long wavelengths. We measured individual differences in chromatic sensitivity to explore the role LCA may play in the development o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138264/ https://www.ncbi.nlm.nih.gov/pubmed/30242363 http://dx.doi.org/10.1167/iovs.18-24113 |
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author | Taylor, Christopher Patrick Shepard, Timothy G. Rucker, Frances J. Eskew, Rhea T. |
author_facet | Taylor, Christopher Patrick Shepard, Timothy G. Rucker, Frances J. Eskew, Rhea T. |
author_sort | Taylor, Christopher Patrick |
collection | PubMed |
description | PURPOSE: Longitudinal chromatic aberration (LCA) is a color signal available to the emmetropization process that causes greater myopic defocus of short wavelengths than long wavelengths. We measured individual differences in chromatic sensitivity to explore the role LCA may play in the development of refractive error. METHODS: Forty-four observers were tested psychophysically after passing color screening tests and a questionnaire for visual defects. Refraction was measured and only subjects with myopia or hyperopia without severe astigmatism participated. Psychophysical detection thresholds for 3 cyc/deg achromatic, L-, M-, and S-cone–isolating Gabor patches and low-frequency S-cone increment (S+) and decrement (S−) blobs were measured. Parametric Pearson correlations for refractive error versus threshold were calculated and nonparametric bootstrap 95% percentage confidence intervals (BCIs) for r were computed. RESULTS: S-cone Gabor detection thresholds were higher than achromatic, L-, and M-cone Gabors. S-cone Gabor thresholds were higher than either S+ or S− blobs. These results are consistent with studies using smaller samples of practiced observers. None of the thresholds for the Gabor stimuli were correlated with refractive error (RE). A negative correlation with RE was observed for both S+ (r = −0.28; P = 0.06; BCI: r = −0.5, −0.04) and S− (r = −0.23; P = 0.13; BCI = −0.46, 0.01) blobs, although this relationship did not reach conventional statistical significance. CONCLUSIONS: Thresholds for S+ and S− stimuli were negatively related to RE, indicating that myopes may have reduced sensitivity to low spatial frequency S-cone stimuli. This reduced S-cone sensitivity might have played a role in their failure to emmetropize normally. |
format | Online Article Text |
id | pubmed-6138264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61382642018-09-17 Sensitivity to S-Cone Stimuli and the Development of Myopia Taylor, Christopher Patrick Shepard, Timothy G. Rucker, Frances J. Eskew, Rhea T. Invest Ophthalmol Vis Sci Visual Psychophysics and Physiological Optics PURPOSE: Longitudinal chromatic aberration (LCA) is a color signal available to the emmetropization process that causes greater myopic defocus of short wavelengths than long wavelengths. We measured individual differences in chromatic sensitivity to explore the role LCA may play in the development of refractive error. METHODS: Forty-four observers were tested psychophysically after passing color screening tests and a questionnaire for visual defects. Refraction was measured and only subjects with myopia or hyperopia without severe astigmatism participated. Psychophysical detection thresholds for 3 cyc/deg achromatic, L-, M-, and S-cone–isolating Gabor patches and low-frequency S-cone increment (S+) and decrement (S−) blobs were measured. Parametric Pearson correlations for refractive error versus threshold were calculated and nonparametric bootstrap 95% percentage confidence intervals (BCIs) for r were computed. RESULTS: S-cone Gabor detection thresholds were higher than achromatic, L-, and M-cone Gabors. S-cone Gabor thresholds were higher than either S+ or S− blobs. These results are consistent with studies using smaller samples of practiced observers. None of the thresholds for the Gabor stimuli were correlated with refractive error (RE). A negative correlation with RE was observed for both S+ (r = −0.28; P = 0.06; BCI: r = −0.5, −0.04) and S− (r = −0.23; P = 0.13; BCI = −0.46, 0.01) blobs, although this relationship did not reach conventional statistical significance. CONCLUSIONS: Thresholds for S+ and S− stimuli were negatively related to RE, indicating that myopes may have reduced sensitivity to low spatial frequency S-cone stimuli. This reduced S-cone sensitivity might have played a role in their failure to emmetropize normally. The Association for Research in Vision and Ophthalmology 2018-09 /pmc/articles/PMC6138264/ /pubmed/30242363 http://dx.doi.org/10.1167/iovs.18-24113 Text en Copyright 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Visual Psychophysics and Physiological Optics Taylor, Christopher Patrick Shepard, Timothy G. Rucker, Frances J. Eskew, Rhea T. Sensitivity to S-Cone Stimuli and the Development of Myopia |
title | Sensitivity to S-Cone Stimuli and the Development of Myopia |
title_full | Sensitivity to S-Cone Stimuli and the Development of Myopia |
title_fullStr | Sensitivity to S-Cone Stimuli and the Development of Myopia |
title_full_unstemmed | Sensitivity to S-Cone Stimuli and the Development of Myopia |
title_short | Sensitivity to S-Cone Stimuli and the Development of Myopia |
title_sort | sensitivity to s-cone stimuli and the development of myopia |
topic | Visual Psychophysics and Physiological Optics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138264/ https://www.ncbi.nlm.nih.gov/pubmed/30242363 http://dx.doi.org/10.1167/iovs.18-24113 |
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