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Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography

PURPOSE: The pathology of Parkinson's disease (PD) is suspected to affect the retina and choroid. We investigated changes in the retina and choroid of patients with PD using optical coherence tomography. METHODS: We examined 14 patients with PD and 22 patients without PD. Patients without PD ha...

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Autores principales: Kamata, Yasuaki, Hara, Naoto, Satou, Tsukasa, Niida, Takahiro, Mukuno, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122847/
https://www.ncbi.nlm.nih.gov/pubmed/34859311
http://dx.doi.org/10.1007/s10792-021-02133-0
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author Kamata, Yasuaki
Hara, Naoto
Satou, Tsukasa
Niida, Takahiro
Mukuno, Kazuo
author_facet Kamata, Yasuaki
Hara, Naoto
Satou, Tsukasa
Niida, Takahiro
Mukuno, Kazuo
author_sort Kamata, Yasuaki
collection PubMed
description PURPOSE: The pathology of Parkinson's disease (PD) is suspected to affect the retina and choroid. We investigated changes in the retina and choroid of patients with PD using optical coherence tomography. METHODS: We examined 14 patients with PD and 22 patients without PD. Patients without PD had no ophthalmic disease other than cataracts. In addition, it was also confirmed that there was no neurodegenerative disease. The retinal nerve fiber layer, ganglion cell layer + inner plexiform layer, and choroidal thickness were compared between both groups. Additionally, the choroidal image was divided into the choroid area, luminal area, and interstitial area using the binarization method, and the area of each region and the percentage of luminal area in the choroid area were analyzed. RESULTS: Patients with PD had a significantly thinner ganglion cell layer + inner plexiform layer compared to those without PD. The choroid area, luminal area, and interstitial area were significantly decreased in patients with PD compared to those without PD. Seven patients with PD who were successfully followed up showed decreased retinal nerve fiber layer and interstitial area after 3 years. CONCLUSION: Autonomic nervous disorders and neurodegeneration in PD can cause thinning of the retina and choroid, as well as a reduction in the choroid area.
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spelling pubmed-91228472022-05-22 Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography Kamata, Yasuaki Hara, Naoto Satou, Tsukasa Niida, Takahiro Mukuno, Kazuo Int Ophthalmol Original Paper PURPOSE: The pathology of Parkinson's disease (PD) is suspected to affect the retina and choroid. We investigated changes in the retina and choroid of patients with PD using optical coherence tomography. METHODS: We examined 14 patients with PD and 22 patients without PD. Patients without PD had no ophthalmic disease other than cataracts. In addition, it was also confirmed that there was no neurodegenerative disease. The retinal nerve fiber layer, ganglion cell layer + inner plexiform layer, and choroidal thickness were compared between both groups. Additionally, the choroidal image was divided into the choroid area, luminal area, and interstitial area using the binarization method, and the area of each region and the percentage of luminal area in the choroid area were analyzed. RESULTS: Patients with PD had a significantly thinner ganglion cell layer + inner plexiform layer compared to those without PD. The choroid area, luminal area, and interstitial area were significantly decreased in patients with PD compared to those without PD. Seven patients with PD who were successfully followed up showed decreased retinal nerve fiber layer and interstitial area after 3 years. CONCLUSION: Autonomic nervous disorders and neurodegeneration in PD can cause thinning of the retina and choroid, as well as a reduction in the choroid area. Springer Netherlands 2021-12-02 2022 /pmc/articles/PMC9122847/ /pubmed/34859311 http://dx.doi.org/10.1007/s10792-021-02133-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Paper
Kamata, Yasuaki
Hara, Naoto
Satou, Tsukasa
Niida, Takahiro
Mukuno, Kazuo
Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title_full Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title_fullStr Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title_full_unstemmed Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title_short Investigation of the pathophysiology of the retina and choroid in Parkinson's disease by optical coherence tomography
title_sort investigation of the pathophysiology of the retina and choroid in parkinson's disease by optical coherence tomography
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122847/
https://www.ncbi.nlm.nih.gov/pubmed/34859311
http://dx.doi.org/10.1007/s10792-021-02133-0
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