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Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study
Spiral drawings on paper are used as routine measures in hospitals to assess Parkinson’s Disease motor deficiencies. In the age of emerging mobile health tools and Artificial Intelligence a comprehensive digital setup enables granular biomarker analyses and improved differential diagnoses in movemen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293248/ https://www.ncbi.nlm.nih.gov/pubmed/37365210 http://dx.doi.org/10.1038/s41598-023-37388-3 |
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author | Purk, Maximilian Fujarski, Michael Becker, Marlon Warnecke, Tobias Varghese, Julian |
author_facet | Purk, Maximilian Fujarski, Michael Becker, Marlon Warnecke, Tobias Varghese, Julian |
author_sort | Purk, Maximilian |
collection | PubMed |
description | Spiral drawings on paper are used as routine measures in hospitals to assess Parkinson’s Disease motor deficiencies. In the age of emerging mobile health tools and Artificial Intelligence a comprehensive digital setup enables granular biomarker analyses and improved differential diagnoses in movement disorders. This study aims to evaluate on discriminatory features among Parkison’s Disease patients, healthy subjects and diverse movement disorders. Overall, 24 Parkinson’s Disease patients, 27 healthy controls and 26 patients with similar differential diagnoses were assessed with a novel tablet-based system. It utilizes an integrative assessment by combining a structured symptoms questionnaire—the Parkinson’s Disease Non-Motor Scale—and 2-handed spiral drawing captured on a tablet device. Three different classification tasks were evaluated: Parkinson’s Disease patients versus healthy control group (Task 1), all Movement disorders versus healthy control group (Task 2) and Parkinson’s Disease patients versus diverse other movement disorder patients (Task 3). To systematically study feature importances of digital biomarkers a Machine Learning classifier is cross-validated and interpreted with SHapley Additive exPlanations (SHAP) values. The number of non-motor symptoms differed significantly for Tasks 1 and 2 but not for Task 3. The proposed drawing features partially differed significantly for all three tasks. The diagnostic accuracy was on average 94.0% in Task 1, 89.4% in Task 2, and 72% in Task 3. While the accuracy in Task 3 only using the symptom questionnaire was close to the baseline, it greatly improved when including the tablet-based features from 60 to 72%. The accuracies for all three tasks were significantly improved by integrating the two modalities. These results show that tablet-based drawing features can not only be captured by consumer grade devices, but also capture specific features to Parkinson’s Disease that significantly improve the diagnostic accuracy compared to the symptom questionnaire. Therefore, the proposed system provides an objective type of disease characterization of movement disorders, which could be utilized for home-based assessments as well. Clinicaltrials.gov Study-ID: NCT03638479. |
format | Online Article Text |
id | pubmed-10293248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102932482023-06-28 Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study Purk, Maximilian Fujarski, Michael Becker, Marlon Warnecke, Tobias Varghese, Julian Sci Rep Article Spiral drawings on paper are used as routine measures in hospitals to assess Parkinson’s Disease motor deficiencies. In the age of emerging mobile health tools and Artificial Intelligence a comprehensive digital setup enables granular biomarker analyses and improved differential diagnoses in movement disorders. This study aims to evaluate on discriminatory features among Parkison’s Disease patients, healthy subjects and diverse movement disorders. Overall, 24 Parkinson’s Disease patients, 27 healthy controls and 26 patients with similar differential diagnoses were assessed with a novel tablet-based system. It utilizes an integrative assessment by combining a structured symptoms questionnaire—the Parkinson’s Disease Non-Motor Scale—and 2-handed spiral drawing captured on a tablet device. Three different classification tasks were evaluated: Parkinson’s Disease patients versus healthy control group (Task 1), all Movement disorders versus healthy control group (Task 2) and Parkinson’s Disease patients versus diverse other movement disorder patients (Task 3). To systematically study feature importances of digital biomarkers a Machine Learning classifier is cross-validated and interpreted with SHapley Additive exPlanations (SHAP) values. The number of non-motor symptoms differed significantly for Tasks 1 and 2 but not for Task 3. The proposed drawing features partially differed significantly for all three tasks. The diagnostic accuracy was on average 94.0% in Task 1, 89.4% in Task 2, and 72% in Task 3. While the accuracy in Task 3 only using the symptom questionnaire was close to the baseline, it greatly improved when including the tablet-based features from 60 to 72%. The accuracies for all three tasks were significantly improved by integrating the two modalities. These results show that tablet-based drawing features can not only be captured by consumer grade devices, but also capture specific features to Parkinson’s Disease that significantly improve the diagnostic accuracy compared to the symptom questionnaire. Therefore, the proposed system provides an objective type of disease characterization of movement disorders, which could be utilized for home-based assessments as well. Clinicaltrials.gov Study-ID: NCT03638479. Nature Publishing Group UK 2023-06-26 /pmc/articles/PMC10293248/ /pubmed/37365210 http://dx.doi.org/10.1038/s41598-023-37388-3 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 Purk, Maximilian Fujarski, Michael Becker, Marlon Warnecke, Tobias Varghese, Julian Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title | Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title_full | Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title_fullStr | Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title_full_unstemmed | Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title_short | Utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
title_sort | utilizing a tablet-based artificial intelligence system to assess movement disorders in a prospective study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293248/ https://www.ncbi.nlm.nih.gov/pubmed/37365210 http://dx.doi.org/10.1038/s41598-023-37388-3 |
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