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OCTA reveals remodeling of the peripheral capillary free zones in normal aging
The retinal neurovascular unit consists of blood vessel endothelial cells, pericytes, neurons, astrocytes, and Müller cells that form the inner retinal blood barrier. A peripheral capillary free zone (pCFZ) represents the distance that oxygen and nutrients must diffuse to reach the neural retina, an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329222/ https://www.ncbi.nlm.nih.gov/pubmed/34341456 http://dx.doi.org/10.1038/s41598-021-95230-0 |
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author | Arthur, Edmund Alber, Jessica Thompson, Louisa I. Sinoff, Stuart Snyder, Peter J. |
author_facet | Arthur, Edmund Alber, Jessica Thompson, Louisa I. Sinoff, Stuart Snyder, Peter J. |
author_sort | Arthur, Edmund |
collection | PubMed |
description | The retinal neurovascular unit consists of blood vessel endothelial cells, pericytes, neurons, astrocytes, and Müller cells that form the inner retinal blood barrier. A peripheral capillary free zone (pCFZ) represents the distance that oxygen and nutrients must diffuse to reach the neural retina, and serves as a metric of retinal tissue oxygenation. The pCFZs are formed based on oxygen saturation in the retinal arterioles and venules. Because retinal arterioles contain a larger concentration of oxygenated blood than venules, there is a reduced need for capillaries to exist closely to arterioles compared to venules. Therefore, in a healthy individual, larger periarteriole CFZs are expected compared to perivenule CFZs. With normal aging, there is atrophy of the inner retinal neurons, and consequently reduced extraction of oxygen and nutrients from the retinal vessels (i.e., increased oxygen saturation). Therefore, we hypothesized that the peripheral CFZ will remodel with normal aging. Using Optical Coherence Tomography Angiography, we showed that the pCFZs do remodel in normal aging with large (perivenule: η(2)(p) = 0.56) and moderate (periarteriole: η(2)(p) = 0.12) effect sizes, opening the possibility that such changes may be further increased by neurodegenerative diseases that adversely impact the health of the retinal neural cell layers. |
format | Online Article Text |
id | pubmed-8329222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83292222021-08-04 OCTA reveals remodeling of the peripheral capillary free zones in normal aging Arthur, Edmund Alber, Jessica Thompson, Louisa I. Sinoff, Stuart Snyder, Peter J. Sci Rep Article The retinal neurovascular unit consists of blood vessel endothelial cells, pericytes, neurons, astrocytes, and Müller cells that form the inner retinal blood barrier. A peripheral capillary free zone (pCFZ) represents the distance that oxygen and nutrients must diffuse to reach the neural retina, and serves as a metric of retinal tissue oxygenation. The pCFZs are formed based on oxygen saturation in the retinal arterioles and venules. Because retinal arterioles contain a larger concentration of oxygenated blood than venules, there is a reduced need for capillaries to exist closely to arterioles compared to venules. Therefore, in a healthy individual, larger periarteriole CFZs are expected compared to perivenule CFZs. With normal aging, there is atrophy of the inner retinal neurons, and consequently reduced extraction of oxygen and nutrients from the retinal vessels (i.e., increased oxygen saturation). Therefore, we hypothesized that the peripheral CFZ will remodel with normal aging. Using Optical Coherence Tomography Angiography, we showed that the pCFZs do remodel in normal aging with large (perivenule: η(2)(p) = 0.56) and moderate (periarteriole: η(2)(p) = 0.12) effect sizes, opening the possibility that such changes may be further increased by neurodegenerative diseases that adversely impact the health of the retinal neural cell layers. Nature Publishing Group UK 2021-08-02 /pmc/articles/PMC8329222/ /pubmed/34341456 http://dx.doi.org/10.1038/s41598-021-95230-0 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 Arthur, Edmund Alber, Jessica Thompson, Louisa I. Sinoff, Stuart Snyder, Peter J. OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title | OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title_full | OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title_fullStr | OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title_full_unstemmed | OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title_short | OCTA reveals remodeling of the peripheral capillary free zones in normal aging |
title_sort | octa reveals remodeling of the peripheral capillary free zones in normal aging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329222/ https://www.ncbi.nlm.nih.gov/pubmed/34341456 http://dx.doi.org/10.1038/s41598-021-95230-0 |
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