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Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder

An objective biomarker to predict the outcome of isolated rapid eye movement sleep behavior disorder (iRBD) is crucial for the management. This study aimed to investigate cognitive signature of brain [(18)F]FDG PET based on deep learning (DL) for evaluating patients with iRBD. Fifty iRBD patients, 1...

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Autores principales: Ryoo, Hyun Gee, Byun, Jung-Ick, Choi, Hongyoon, Jung, Ki-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649732/
https://www.ncbi.nlm.nih.gov/pubmed/36357491
http://dx.doi.org/10.1038/s41598-022-23347-x
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author Ryoo, Hyun Gee
Byun, Jung-Ick
Choi, Hongyoon
Jung, Ki-Young
author_facet Ryoo, Hyun Gee
Byun, Jung-Ick
Choi, Hongyoon
Jung, Ki-Young
author_sort Ryoo, Hyun Gee
collection PubMed
description An objective biomarker to predict the outcome of isolated rapid eye movement sleep behavior disorder (iRBD) is crucial for the management. This study aimed to investigate cognitive signature of brain [(18)F]FDG PET based on deep learning (DL) for evaluating patients with iRBD. Fifty iRBD patients, 19 with mild cognitive impairment (MCI) (RBD-MCI) and 31 without MCI (RBD-nonMCI), were prospectively enrolled. A DL model for the cognitive signature was trained by using Alzheimer’s Disease Neuroimaging Initiative database and transferred to baseline [(18)F]FDG PET from the iRBD cohort. The results showed that the DL-based cognitive dysfunction score was significantly higher in RBD-MCI than in RBD-nonMCI. The AUC of ROC curve for differentiating RBD-MCI from RBD-nonMCI was 0.70 (95% CI 0.56–0.82). The baseline DL-based cognitive dysfunction score was significantly higher in iRBD patients who showed a decrease in CERAD scores during 2 years than in those who did not. Brain metabolic features related to cognitive dysfunction-related regions of individual iRBD patients mainly included posterior cortical regions. This work demonstrates that the cognitive signature based on DL could be used to objectively evaluate cognitive function in iRBD. We suggest that this approach could be extended to an objective biomarker predicting cognitive decline and neurodegeneration in iRBD.
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spelling pubmed-96497322022-11-15 Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder Ryoo, Hyun Gee Byun, Jung-Ick Choi, Hongyoon Jung, Ki-Young Sci Rep Article An objective biomarker to predict the outcome of isolated rapid eye movement sleep behavior disorder (iRBD) is crucial for the management. This study aimed to investigate cognitive signature of brain [(18)F]FDG PET based on deep learning (DL) for evaluating patients with iRBD. Fifty iRBD patients, 19 with mild cognitive impairment (MCI) (RBD-MCI) and 31 without MCI (RBD-nonMCI), were prospectively enrolled. A DL model for the cognitive signature was trained by using Alzheimer’s Disease Neuroimaging Initiative database and transferred to baseline [(18)F]FDG PET from the iRBD cohort. The results showed that the DL-based cognitive dysfunction score was significantly higher in RBD-MCI than in RBD-nonMCI. The AUC of ROC curve for differentiating RBD-MCI from RBD-nonMCI was 0.70 (95% CI 0.56–0.82). The baseline DL-based cognitive dysfunction score was significantly higher in iRBD patients who showed a decrease in CERAD scores during 2 years than in those who did not. Brain metabolic features related to cognitive dysfunction-related regions of individual iRBD patients mainly included posterior cortical regions. This work demonstrates that the cognitive signature based on DL could be used to objectively evaluate cognitive function in iRBD. We suggest that this approach could be extended to an objective biomarker predicting cognitive decline and neurodegeneration in iRBD. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9649732/ /pubmed/36357491 http://dx.doi.org/10.1038/s41598-022-23347-x 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
Ryoo, Hyun Gee
Byun, Jung-Ick
Choi, Hongyoon
Jung, Ki-Young
Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title_full Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title_fullStr Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title_full_unstemmed Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title_short Deep learning signature of brain [(18)F]FDG PET associated with cognitive outcome of rapid eye movement sleep behavior disorder
title_sort deep learning signature of brain [(18)f]fdg pet associated with cognitive outcome of rapid eye movement sleep behavior disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649732/
https://www.ncbi.nlm.nih.gov/pubmed/36357491
http://dx.doi.org/10.1038/s41598-022-23347-x
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