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Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease
We investigated the association between retinal changes measured using optical coherence tomography (OCT) and diverse clinical grading scales in patients with Parkinson’s disease (PD). Seventy-four eyes of 74 patients with de novo PD and 53 eyes of age-matched control subjects were included. The thi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694167/ https://www.ncbi.nlm.nih.gov/pubmed/31413302 http://dx.doi.org/10.1038/s41598-019-48388-7 |
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author | Sung, Mi Sun Choi, Seong-Min Kim, Jonghwa Ha, Jun Young Kim, Byeong-Chae Heo, Hwan Park, Sang Woo |
author_facet | Sung, Mi Sun Choi, Seong-Min Kim, Jonghwa Ha, Jun Young Kim, Byeong-Chae Heo, Hwan Park, Sang Woo |
author_sort | Sung, Mi Sun |
collection | PubMed |
description | We investigated the association between retinal changes measured using optical coherence tomography (OCT) and diverse clinical grading scales in patients with Parkinson’s disease (PD). Seventy-four eyes of 74 patients with de novo PD and 53 eyes of age-matched control subjects were included. The thickness of the peripapillary retinal nerve fiber layer (pRNFL) and macular ganglion cell-inner plexiform layer (mGCIPL) were measured. We analyzed the correlations between the clinical PD grading scales and OCT parameters, and between the OCT parameters and volumetric data in the cerebral cortical and subcortical structures. The area under the receiver operating characteristic curve (AUC) was calculated for diagnosing cognitive impairment in patients with PD. Statistically significant reductions in the thickness of average, temporal, and inferior pRNFL and overall mGCIPL were observed in patients with PD. The Montreal Cognitive Assessment score was significantly associated with mGCIPL thinning. The AUC of the mGCIPL parameters for diagnosing cognitive impairment in patients with PD ranged from 0.651 to 0.760. Moreover, thinning of the mGCIPL was significantly associated with the volumetric parameters of associated brain structures. Our findings highlight the clinical implications of OCT measurements as a potential biomarker for early detection of cognitive impairment in patients with PD. |
format | Online Article Text |
id | pubmed-6694167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66941672019-08-19 Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease Sung, Mi Sun Choi, Seong-Min Kim, Jonghwa Ha, Jun Young Kim, Byeong-Chae Heo, Hwan Park, Sang Woo Sci Rep Article We investigated the association between retinal changes measured using optical coherence tomography (OCT) and diverse clinical grading scales in patients with Parkinson’s disease (PD). Seventy-four eyes of 74 patients with de novo PD and 53 eyes of age-matched control subjects were included. The thickness of the peripapillary retinal nerve fiber layer (pRNFL) and macular ganglion cell-inner plexiform layer (mGCIPL) were measured. We analyzed the correlations between the clinical PD grading scales and OCT parameters, and between the OCT parameters and volumetric data in the cerebral cortical and subcortical structures. The area under the receiver operating characteristic curve (AUC) was calculated for diagnosing cognitive impairment in patients with PD. Statistically significant reductions in the thickness of average, temporal, and inferior pRNFL and overall mGCIPL were observed in patients with PD. The Montreal Cognitive Assessment score was significantly associated with mGCIPL thinning. The AUC of the mGCIPL parameters for diagnosing cognitive impairment in patients with PD ranged from 0.651 to 0.760. Moreover, thinning of the mGCIPL was significantly associated with the volumetric parameters of associated brain structures. Our findings highlight the clinical implications of OCT measurements as a potential biomarker for early detection of cognitive impairment in patients with PD. Nature Publishing Group UK 2019-08-14 /pmc/articles/PMC6694167/ /pubmed/31413302 http://dx.doi.org/10.1038/s41598-019-48388-7 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sung, Mi Sun Choi, Seong-Min Kim, Jonghwa Ha, Jun Young Kim, Byeong-Chae Heo, Hwan Park, Sang Woo Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title | Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title_full | Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title_fullStr | Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title_full_unstemmed | Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title_short | Inner retinal thinning as a biomarker for cognitive impairment in de novo Parkinson’s disease |
title_sort | inner retinal thinning as a biomarker for cognitive impairment in de novo parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694167/ https://www.ncbi.nlm.nih.gov/pubmed/31413302 http://dx.doi.org/10.1038/s41598-019-48388-7 |
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