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Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction
Tractional tethering by the optic nerve (ON) on the eye as it rotates towards the midline in adduction is a significant ocular mechanical load and has been suggested as a cause of ON damage induced by repetitive eye movements. We designed an ocular finite element model (FEM) simulating 6° incrementa...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643519/ https://www.ncbi.nlm.nih.gov/pubmed/36347907 http://dx.doi.org/10.1038/s41598-022-22899-2 |
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author | Park, Joseph Shin, Andrew Demer, Joseph L. |
author_facet | Park, Joseph Shin, Andrew Demer, Joseph L. |
author_sort | Park, Joseph |
collection | PubMed |
description | Tractional tethering by the optic nerve (ON) on the eye as it rotates towards the midline in adduction is a significant ocular mechanical load and has been suggested as a cause of ON damage induced by repetitive eye movements. We designed an ocular finite element model (FEM) simulating 6° incremental adduction beyond the initial configuration of 26° adduction that is the observed threshold for ON tethering. This FEM permitted sensitivity analysis of ON tethering using observed material property variations in measured hyperelasticity of the anterior, equatorial, posterior, and peripapillary sclera; and the ON and its sheath. The FEM predicted that adduction beyond the initiation of ON tethering concentrates stress and strain on the temporal side of the optic disc and peripapillary sclera, the ON sheath junction with the sclera, and retrolaminar ON neural tissue. However, some unfavorable combinations of tissue properties within the published ranges imposed higher stresses in these regions. With the least favorable combinations of tissue properties, adduction tethering was predicted to stress the ON junction and peripapillary sclera more than extreme conditions of intraocular and intracranial pressure. These simulations support the concept that ON tethering in adduction could induce mechanical stresses that might contribute to ON damage. |
format | Online Article Text |
id | pubmed-9643519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96435192022-11-15 Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction Park, Joseph Shin, Andrew Demer, Joseph L. Sci Rep Article Tractional tethering by the optic nerve (ON) on the eye as it rotates towards the midline in adduction is a significant ocular mechanical load and has been suggested as a cause of ON damage induced by repetitive eye movements. We designed an ocular finite element model (FEM) simulating 6° incremental adduction beyond the initial configuration of 26° adduction that is the observed threshold for ON tethering. This FEM permitted sensitivity analysis of ON tethering using observed material property variations in measured hyperelasticity of the anterior, equatorial, posterior, and peripapillary sclera; and the ON and its sheath. The FEM predicted that adduction beyond the initiation of ON tethering concentrates stress and strain on the temporal side of the optic disc and peripapillary sclera, the ON sheath junction with the sclera, and retrolaminar ON neural tissue. However, some unfavorable combinations of tissue properties within the published ranges imposed higher stresses in these regions. With the least favorable combinations of tissue properties, adduction tethering was predicted to stress the ON junction and peripapillary sclera more than extreme conditions of intraocular and intracranial pressure. These simulations support the concept that ON tethering in adduction could induce mechanical stresses that might contribute to ON damage. Nature Publishing Group UK 2022-11-08 /pmc/articles/PMC9643519/ /pubmed/36347907 http://dx.doi.org/10.1038/s41598-022-22899-2 Text en © The Author(s) 2022 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 Park, Joseph Shin, Andrew Demer, Joseph L. Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title | Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title_full | Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title_fullStr | Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title_full_unstemmed | Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title_short | Finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
title_sort | finite element modeling of effects of tissue property variation on human optic nerve tethering during adduction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643519/ https://www.ncbi.nlm.nih.gov/pubmed/36347907 http://dx.doi.org/10.1038/s41598-022-22899-2 |
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