Visual callosal topography in the absence of retinal input
Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal “waves” of spontaneous activity similar to those of sighted subjects, and on...
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Published in | NeuroImage (Orlando, Fla.) Vol. 81; pp. 325 - 334 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Inc
01.11.2013
Elsevier Elsevier Limited |
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Online Access | Get full text |
ISSN | 1053-8119 1095-9572 1095-9572 |
DOI | 10.1016/j.neuroimage.2013.05.038 |
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Abstract | Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal “waves” of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium.
•Topographic organization within the splenium is robust to loss of retinal input.•Splenial volume is not reduced in anophthalmic or early blind subjects.•Measures of splenial diffusivity are not altered due to early blindness. |
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AbstractList | Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal awavesa of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium. Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal "waves" of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium.Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal "waves" of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium. Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal “waves” of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium. •Topographic organization within the splenium is robust to loss of retinal input.•Splenial volume is not reduced in anophthalmic or early blind subjects.•Measures of splenial diffusivity are not altered due to early blindness. Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal "waves" of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, though some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience plays a role in the large-scale topographic organization of visual callosal connections within the splenium. Using probabilistic diffusion tractography, we examined the retinotopic organization of splenial callosal connections within early blind, anophthalmic, and control subjects. Early blind subjects experienced prenatal retinal “waves” of spontaneous activity similar to those of sighted subjects, and only lack postnatal visual experience. In anophthalmia, the eye is either absent or arrested at an early prenatal stage, depriving these subjects of both pre- and postnatal visual input. Therefore, comparing these two groups provides a way of separating the influence of pre- and postnatal retinal input on the organization of visual connections across hemispheres. We found that retinotopic mapping within the splenium was not measurably disrupted in early blind or anophthalmic subjects compared to visually normal controls. No significant differences in splenial volume were observed across groups. No significant differences in diffusivity were found between early blind subjects and sighted controls, through some differences in diffusivity were noted between anophthalmic subjects and controls. These results suggest that neither prenatal retinal activity nor postnatal visual experience play a role in the large-scale topographic organization of visual callosal connections within the splenium. |
Author | Fine, Ione Saenz, Melissa Tungaraza, Rosalia Boynton, Geoffrey M. Bridge, Holly Bock, Andrew S. |
AuthorAffiliation | c Integrated Brain Imaging Center (IBIC), Department of Radiology, University of Washington, Seattle, WA 98195, USA b Department of Clinical Neuroscience, University of Lausanne, 1011 Lausanne, Switzerland d FMRIB Centre, Clinical Neurosciences, University of Oxford, Oxford, OX3 9DU, United Kingdom a Department of Psychology, University of Washington, Seattle, WA 98195, USA |
AuthorAffiliation_xml | – name: a Department of Psychology, University of Washington, Seattle, WA 98195, USA – name: b Department of Clinical Neuroscience, University of Lausanne, 1011 Lausanne, Switzerland – name: c Integrated Brain Imaging Center (IBIC), Department of Radiology, University of Washington, Seattle, WA 98195, USA – name: d FMRIB Centre, Clinical Neurosciences, University of Oxford, Oxford, OX3 9DU, United Kingdom |
Author_xml | – sequence: 1 givenname: Andrew S. surname: Bock fullname: Bock, Andrew S. email: abock@u.washington.edu organization: Department of Psychology, University of Washington, Seattle, WA 98195, USA – sequence: 2 givenname: Melissa surname: Saenz fullname: Saenz, Melissa organization: Department of Clinical Neuroscience, University of Lausanne, 1011 Lausanne, Switzerland – sequence: 3 givenname: Rosalia surname: Tungaraza fullname: Tungaraza, Rosalia organization: Integrated Brain Imaging Center (IBIC), Department of Radiology, University of Washington, Seattle, WA 98195, USA – sequence: 4 givenname: Geoffrey M. surname: Boynton fullname: Boynton, Geoffrey M. organization: Department of Psychology, University of Washington, Seattle, WA 98195, USA – sequence: 5 givenname: Holly surname: Bridge fullname: Bridge, Holly organization: FMRIB Centre, Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, United Kingdom – sequence: 6 givenname: Ione surname: Fine fullname: Fine, Ione organization: Department of Psychology, University of Washington, Seattle, WA 98195, USA |
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Keywords | Development Blind Anophthalmia Tractography Plasticity Diffusion tensor imaging Eye Visual system Retina |
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SubjectTerms | Adult Age Anophthalmia Anophthalmos - pathology Biological and medical sciences Blind Blindness - pathology Brain Corpus Callosum - pathology Development Diffusion Tensor Imaging Eye and associated structures. Visual pathways and centers. Vision Female Fundamental and applied biological sciences. Psychology Humans Image Processing, Computer-Assisted Male Middle Aged Plasticity Retina - physiopathology Scanners Studies Tractography Vertebrates: nervous system and sense organs Visual Pathways - pathology Young Adult |
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Title | Visual callosal topography in the absence of retinal input |
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