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Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features
Patients with Parkinson’s Disease (PD) often suffer from cognitive decline. Accurate prediction of cognitive decline is essential for early treatment of at-risk patients. The aim of this study was to develop and evaluate a multimodal machine learning model for the prediction of continuous cognitive...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425414/ https://www.ncbi.nlm.nih.gov/pubmed/37580407 http://dx.doi.org/10.1038/s41598-023-37644-6 |
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author | Almgren, Hannes Camacho, Milton Hanganu, Alexandru Kibreab, Mekale Camicioli, Richard Ismail, Zahinoor Forkert, Nils D. Monchi, Oury |
author_facet | Almgren, Hannes Camacho, Milton Hanganu, Alexandru Kibreab, Mekale Camicioli, Richard Ismail, Zahinoor Forkert, Nils D. Monchi, Oury |
author_sort | Almgren, Hannes |
collection | PubMed |
description | Patients with Parkinson’s Disease (PD) often suffer from cognitive decline. Accurate prediction of cognitive decline is essential for early treatment of at-risk patients. The aim of this study was to develop and evaluate a multimodal machine learning model for the prediction of continuous cognitive decline in patients with early PD. We included 213 PD patients from the Parkinson’s Progression Markers Initiative (PPMI) database. Machine learning was used to predict change in Montreal Cognitive Assessment (MoCA) score using the difference between baseline and 4-years follow-up data as outcome. Input features were categorized into four sets: clinical test scores, cerebrospinal fluid (CSF) biomarkers, brain volumes, and genetic variants. All combinations of input feature sets were added to a basic model, which consisted of demographics and baseline cognition. An iterative scheme using RReliefF-based feature ranking and support vector regression in combination with tenfold cross validation was used to determine the optimal number of predictive features and to evaluate model performance for each combination of input feature sets. Our best performing model consisted of a combination of the basic model, clinical test scores and CSF-based biomarkers. This model had 12 features, which included baseline cognition, CSF phosphorylated tau, CSF total tau, CSF amyloid-beta(1-42), geriatric depression scale (GDS) scores, and anxiety scores. Interestingly, many of the predictive features in our model have previously been associated with Alzheimer’s disease, showing the importance of assessing Alzheimer’s disease pathology in patients with Parkinson’s disease. |
format | Online Article Text |
id | pubmed-10425414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104254142023-08-16 Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features Almgren, Hannes Camacho, Milton Hanganu, Alexandru Kibreab, Mekale Camicioli, Richard Ismail, Zahinoor Forkert, Nils D. Monchi, Oury Sci Rep Article Patients with Parkinson’s Disease (PD) often suffer from cognitive decline. Accurate prediction of cognitive decline is essential for early treatment of at-risk patients. The aim of this study was to develop and evaluate a multimodal machine learning model for the prediction of continuous cognitive decline in patients with early PD. We included 213 PD patients from the Parkinson’s Progression Markers Initiative (PPMI) database. Machine learning was used to predict change in Montreal Cognitive Assessment (MoCA) score using the difference between baseline and 4-years follow-up data as outcome. Input features were categorized into four sets: clinical test scores, cerebrospinal fluid (CSF) biomarkers, brain volumes, and genetic variants. All combinations of input feature sets were added to a basic model, which consisted of demographics and baseline cognition. An iterative scheme using RReliefF-based feature ranking and support vector regression in combination with tenfold cross validation was used to determine the optimal number of predictive features and to evaluate model performance for each combination of input feature sets. Our best performing model consisted of a combination of the basic model, clinical test scores and CSF-based biomarkers. This model had 12 features, which included baseline cognition, CSF phosphorylated tau, CSF total tau, CSF amyloid-beta(1-42), geriatric depression scale (GDS) scores, and anxiety scores. Interestingly, many of the predictive features in our model have previously been associated with Alzheimer’s disease, showing the importance of assessing Alzheimer’s disease pathology in patients with Parkinson’s disease. Nature Publishing Group UK 2023-08-14 /pmc/articles/PMC10425414/ /pubmed/37580407 http://dx.doi.org/10.1038/s41598-023-37644-6 Text en © The Author(s) 2023 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 Almgren, Hannes Camacho, Milton Hanganu, Alexandru Kibreab, Mekale Camicioli, Richard Ismail, Zahinoor Forkert, Nils D. Monchi, Oury Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title | Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title_full | Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title_fullStr | Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title_full_unstemmed | Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title_short | Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal features |
title_sort | machine learning-based prediction of longitudinal cognitive decline in early parkinson’s disease using multimodal features |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425414/ https://www.ncbi.nlm.nih.gov/pubmed/37580407 http://dx.doi.org/10.1038/s41598-023-37644-6 |
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