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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...

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Autores principales: Sung, Mi Sun, Choi, Seong-Min, Kim, Jonghwa, Ha, Jun Young, Kim, Byeong-Chae, Heo, Hwan, Park, Sang Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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