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Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders

INTRODUCTION: Our aim is to develop a novel approach to hyperkinetic movement disorder classification, that combines clinical information, electromyography, accelerometry and video in a computer-aided classification tool. We see this as the next step towards rapid and accurate phenotype classificati...

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Autores principales: van der Stouwe, A. M. Madelein, Tuitert, Inge, Giotis, Ioannis, Calon, Joost, Gannamani, Rahul, Dalenberg, Jelle R., van der Veen, Sterre, Klamer, Marrit R., Telea, Alex C., Tijssen, Marina A.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506849/
https://www.ncbi.nlm.nih.gov/pubmed/34635535
http://dx.doi.org/10.1136/bmjopen-2021-055068
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author van der Stouwe, A. M. Madelein
Tuitert, Inge
Giotis, Ioannis
Calon, Joost
Gannamani, Rahul
Dalenberg, Jelle R.
van der Veen, Sterre
Klamer, Marrit R.
Telea, Alex C.
Tijssen, Marina A.J.
author_facet van der Stouwe, A. M. Madelein
Tuitert, Inge
Giotis, Ioannis
Calon, Joost
Gannamani, Rahul
Dalenberg, Jelle R.
van der Veen, Sterre
Klamer, Marrit R.
Telea, Alex C.
Tijssen, Marina A.J.
author_sort van der Stouwe, A. M. Madelein
collection PubMed
description INTRODUCTION: Our aim is to develop a novel approach to hyperkinetic movement disorder classification, that combines clinical information, electromyography, accelerometry and video in a computer-aided classification tool. We see this as the next step towards rapid and accurate phenotype classification, the cornerstone of both the diagnostic and treatment process. METHODS AND ANALYSIS: The Next Move in Movement Disorders (NEMO) study is a cross-sectional study at Expertise Centre Movement Disorders Groningen, University Medical Centre Groningen. It comprises patients with single and mixed phenotype movement disorders. Single phenotype groups will first include dystonia, myoclonus and tremor, and then chorea, tics, ataxia and spasticity. Mixed phenotypes are myoclonus-dystonia, dystonic tremor, myoclonus ataxia and jerky/tremulous functional movement disorders. Groups will contain 20 patients, or 40 healthy participants. The gold standard for inclusion consists of interobserver agreement on the phenotype among three independent clinical experts. Electromyography, accelerometry and three-dimensional video data will be recorded during performance of a set of movement tasks, chosen by a team of specialists to elicit movement disorders. These data will serve as input for the machine learning algorithm. Labels for supervised learning are provided by the expert-based classification, allowing the algorithm to learn to predict what the output label should be when given new input data. Methods using manually engineered features based on existing clinical knowledge will be used, as well as deep learning methods which can detect relevant and possibly new features. Finally, we will employ visual analytics to visualise how the classification algorithm arrives at its decision. ETHICS AND DISSEMINATION: Ethical approval has been obtained from the relevant local ethics committee. The NEMO study is designed to pioneer the application of machine learning of movement disorders. We expect to publish articles in multiple related fields of research and patients will be informed of important results via patient associations and press releases.
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spelling pubmed-85068492021-10-22 Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders van der Stouwe, A. M. Madelein Tuitert, Inge Giotis, Ioannis Calon, Joost Gannamani, Rahul Dalenberg, Jelle R. van der Veen, Sterre Klamer, Marrit R. Telea, Alex C. Tijssen, Marina A.J. BMJ Open Neurology INTRODUCTION: Our aim is to develop a novel approach to hyperkinetic movement disorder classification, that combines clinical information, electromyography, accelerometry and video in a computer-aided classification tool. We see this as the next step towards rapid and accurate phenotype classification, the cornerstone of both the diagnostic and treatment process. METHODS AND ANALYSIS: The Next Move in Movement Disorders (NEMO) study is a cross-sectional study at Expertise Centre Movement Disorders Groningen, University Medical Centre Groningen. It comprises patients with single and mixed phenotype movement disorders. Single phenotype groups will first include dystonia, myoclonus and tremor, and then chorea, tics, ataxia and spasticity. Mixed phenotypes are myoclonus-dystonia, dystonic tremor, myoclonus ataxia and jerky/tremulous functional movement disorders. Groups will contain 20 patients, or 40 healthy participants. The gold standard for inclusion consists of interobserver agreement on the phenotype among three independent clinical experts. Electromyography, accelerometry and three-dimensional video data will be recorded during performance of a set of movement tasks, chosen by a team of specialists to elicit movement disorders. These data will serve as input for the machine learning algorithm. Labels for supervised learning are provided by the expert-based classification, allowing the algorithm to learn to predict what the output label should be when given new input data. Methods using manually engineered features based on existing clinical knowledge will be used, as well as deep learning methods which can detect relevant and possibly new features. Finally, we will employ visual analytics to visualise how the classification algorithm arrives at its decision. ETHICS AND DISSEMINATION: Ethical approval has been obtained from the relevant local ethics committee. The NEMO study is designed to pioneer the application of machine learning of movement disorders. We expect to publish articles in multiple related fields of research and patients will be informed of important results via patient associations and press releases. BMJ Publishing Group 2021-10-11 /pmc/articles/PMC8506849/ /pubmed/34635535 http://dx.doi.org/10.1136/bmjopen-2021-055068 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Neurology
van der Stouwe, A. M. Madelein
Tuitert, Inge
Giotis, Ioannis
Calon, Joost
Gannamani, Rahul
Dalenberg, Jelle R.
van der Veen, Sterre
Klamer, Marrit R.
Telea, Alex C.
Tijssen, Marina A.J.
Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title_full Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title_fullStr Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title_full_unstemmed Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title_short Next move in movement disorders (NEMO): developing a computer-aided classification tool for hyperkinetic movement disorders
title_sort next move in movement disorders (nemo): developing a computer-aided classification tool for hyperkinetic movement disorders
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506849/
https://www.ncbi.nlm.nih.gov/pubmed/34635535
http://dx.doi.org/10.1136/bmjopen-2021-055068
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