Discriminating progressive supranuclear palsy from Parkinson's disease using wearable technology and machine learning.


Journal

Gait & posture
ISSN: 1879-2219
Titre abrégé: Gait Posture
Pays: England
ID NLM: 9416830

Informations de publication

Date de publication:
03 2020
Historique:
received: 27 09 2019
revised: 05 02 2020
accepted: 06 02 2020
pubmed: 23 2 2020
medline: 1 12 2020
entrez: 21 2 2020
Statut: ppublish

Résumé

Progressive supranuclear palsy (PSP), a neurodegenerative conditions may be difficult to discriminate clinically from idiopathic Parkinson's disease (PD). It is critical that we are able to do this accurately and as early as possible in order that future disease modifying therapies for PSP may be deployed at a stage when they are likely to have maximal benefit. Analysis of gait and related tasks is one possible means of discrimination. Here we investigate a wearable sensor array coupled with machine learning approaches as a means of disease classification. 21 participants with PSP, 20 with PD, and 39 healthy control (HC) subjects performed a two minute walk, static sway test, and timed up-and-go task, while wearing an array of six inertial measurement units. The data were analysed to determine what features discriminated PSP from PD and PSP from HC. Two machine learning algorithms were applied, Logistic Regression (LR) and Random Forest (RF). 17 features were identified in the combined dataset that contained independent information. The RF classifier outperformed the LR classifier, and allowed discrimination of PSP from PD with 86 % sensitivity and 90 % specificity, and PSP from HC with 90 % sensitivity and 97 % specificity. Using data from the single lumbar sensor only resulted in only a modest reduction in classification accuracy, which could be restored using 3 sensors (lumbar, right arm and foot). However for maximum specificity the full six sensor array was needed. A wearable sensor array coupled with machine learning methods can accurately discriminate PSP from PD. Choice of array complexity depends on context; for diagnostic purposes a high specificity is needed suggesting the more complete array is advantageous, while for subsequent disease tracking a simpler system may suffice.

Sections du résumé

BACKGROUND
Progressive supranuclear palsy (PSP), a neurodegenerative conditions may be difficult to discriminate clinically from idiopathic Parkinson's disease (PD). It is critical that we are able to do this accurately and as early as possible in order that future disease modifying therapies for PSP may be deployed at a stage when they are likely to have maximal benefit. Analysis of gait and related tasks is one possible means of discrimination.
RESEARCH QUESTION
Here we investigate a wearable sensor array coupled with machine learning approaches as a means of disease classification.
METHODS
21 participants with PSP, 20 with PD, and 39 healthy control (HC) subjects performed a two minute walk, static sway test, and timed up-and-go task, while wearing an array of six inertial measurement units. The data were analysed to determine what features discriminated PSP from PD and PSP from HC. Two machine learning algorithms were applied, Logistic Regression (LR) and Random Forest (RF).
RESULTS
17 features were identified in the combined dataset that contained independent information. The RF classifier outperformed the LR classifier, and allowed discrimination of PSP from PD with 86 % sensitivity and 90 % specificity, and PSP from HC with 90 % sensitivity and 97 % specificity. Using data from the single lumbar sensor only resulted in only a modest reduction in classification accuracy, which could be restored using 3 sensors (lumbar, right arm and foot). However for maximum specificity the full six sensor array was needed.
SIGNIFICANCE
A wearable sensor array coupled with machine learning methods can accurately discriminate PSP from PD. Choice of array complexity depends on context; for diagnostic purposes a high specificity is needed suggesting the more complete array is advantageous, while for subsequent disease tracking a simpler system may suffice.

Identifiants

pubmed: 32078894
pii: S0966-6362(20)30068-0
doi: 10.1016/j.gaitpost.2020.02.007
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

257-263

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Crown Copyright © 2020. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest MDV, JP, TB, and CAA have no conflicts of interest. JJF has performed consultancy unrelated to the subject of this study for companies including Abbott, Renishaw, and Herantis, and also has a research grant from Abbott, for a project unrelated to this study.

Auteurs

Maarten De Vos (M)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Old Road Campus Research Building, OX3 7DQ, Oxford, UK.

John Prince (J)

Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Old Road Campus Research Building, OX3 7DQ, Oxford, UK.

Tim Buchanan (T)

UCB Biopharma SPRL, Brussels, Belgium.

James J FitzGerald (JJ)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford, OX3 9DU, UK; Nuffield Department of Clinical Neurosciences, NeuroMetrology Lab, University of Oxford, Oxford, OX3 9DU, UK.

Chrystalina A Antoniades (CA)

Nuffield Department of Clinical Neurosciences, NeuroMetrology Lab, University of Oxford, Oxford, OX3 9DU, UK. Electronic address: chrystalina.antoniades@ndcn.ox.ac.uk.

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