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Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease

To evaluate the significance of motion artifacts in optical coherence tomography angiography (OCTA) images of patients with Parkinson’s disease (PD) and healthy controls. In this prospective, cross-sectional study subjects with medicated PD (ON) and healthy, age- and gender-matched volunteers were r...

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Autores principales: Lauermann, Jost L., Sochurek, Jan A. M., Plöttner, Pauline, Alten, Florian, Kasten, Meike, Prasuhn, Jannik, Brüggemann, Norbert, Ranjbar, Mahdy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943590/
https://www.ncbi.nlm.nih.gov/pubmed/33750844
http://dx.doi.org/10.1038/s41598-021-84862-x
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author Lauermann, Jost L.
Sochurek, Jan A. M.
Plöttner, Pauline
Alten, Florian
Kasten, Meike
Prasuhn, Jannik
Brüggemann, Norbert
Ranjbar, Mahdy
author_facet Lauermann, Jost L.
Sochurek, Jan A. M.
Plöttner, Pauline
Alten, Florian
Kasten, Meike
Prasuhn, Jannik
Brüggemann, Norbert
Ranjbar, Mahdy
author_sort Lauermann, Jost L.
collection PubMed
description To evaluate the significance of motion artifacts in optical coherence tomography angiography (OCTA) images of patients with Parkinson’s disease (PD) and healthy controls. In this prospective, cross-sectional study subjects with medicated PD (ON) and healthy, age- and gender-matched volunteers were recruited. Participants underwent specific ophthalmological examinations, including OCTA. Angiograms of the superficial retinal capillary plexus were evaluated for the type and frequency of artifacts using a validated motion artifact score (MAS). A total of 30 PD patients (60 eyes), average disease duration of 9.61 ± 5.55 years, and 30 matched, healthy controls (60 eyes) were recruited. Twenty percent of all eyes had an eye disease, unknown to the participant, with a significant impact on OCTA results. After cleansing the dataset by excluding subjects with confounding ocular comorbidities 42 eyes of 28 PD patients and 53 eyes of 29 healthy controls were further evaluated. Overall MAS and all five subtypes of motion artifacts were comparable without significant differences between groups. OCTA can be used in treated PD patients (ON) without a significant increase in motion artifacts. Nevertheless, special attention should be paid to image quality during the acquisition of OCTA data, for which an experienced OCTA operator is useful.
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spelling pubmed-79435902021-03-10 Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease Lauermann, Jost L. Sochurek, Jan A. M. Plöttner, Pauline Alten, Florian Kasten, Meike Prasuhn, Jannik Brüggemann, Norbert Ranjbar, Mahdy Sci Rep Article To evaluate the significance of motion artifacts in optical coherence tomography angiography (OCTA) images of patients with Parkinson’s disease (PD) and healthy controls. In this prospective, cross-sectional study subjects with medicated PD (ON) and healthy, age- and gender-matched volunteers were recruited. Participants underwent specific ophthalmological examinations, including OCTA. Angiograms of the superficial retinal capillary plexus were evaluated for the type and frequency of artifacts using a validated motion artifact score (MAS). A total of 30 PD patients (60 eyes), average disease duration of 9.61 ± 5.55 years, and 30 matched, healthy controls (60 eyes) were recruited. Twenty percent of all eyes had an eye disease, unknown to the participant, with a significant impact on OCTA results. After cleansing the dataset by excluding subjects with confounding ocular comorbidities 42 eyes of 28 PD patients and 53 eyes of 29 healthy controls were further evaluated. Overall MAS and all five subtypes of motion artifacts were comparable without significant differences between groups. OCTA can be used in treated PD patients (ON) without a significant increase in motion artifacts. Nevertheless, special attention should be paid to image quality during the acquisition of OCTA data, for which an experienced OCTA operator is useful. Nature Publishing Group UK 2021-03-09 /pmc/articles/PMC7943590/ /pubmed/33750844 http://dx.doi.org/10.1038/s41598-021-84862-x Text en © The Author(s) 2021 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/.
spellingShingle Article
Lauermann, Jost L.
Sochurek, Jan A. M.
Plöttner, Pauline
Alten, Florian
Kasten, Meike
Prasuhn, Jannik
Brüggemann, Norbert
Ranjbar, Mahdy
Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title_full Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title_fullStr Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title_full_unstemmed Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title_short Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease
title_sort applicability of optical coherence tomography angiography (octa) imaging in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943590/
https://www.ncbi.nlm.nih.gov/pubmed/33750844
http://dx.doi.org/10.1038/s41598-021-84862-x
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