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Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease

OBJECTIVES: Parkinson’s disease (PD) is the second most common neurodegenerative disorder; it affects more than 10 million people worldwide. Detecting PD usually requires a professional assessment by an expert, and investigation of the voice as a biomarker of the disease could be effective in speedi...

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Autores principales: Tougui, Ilias, Jilbab, Abdelilah, El Mhamdi, Jamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Medical Informatics 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674819/
https://www.ncbi.nlm.nih.gov/pubmed/33190461
http://dx.doi.org/10.4258/hir.2020.26.4.274
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author Tougui, Ilias
Jilbab, Abdelilah
El Mhamdi, Jamal
author_facet Tougui, Ilias
Jilbab, Abdelilah
El Mhamdi, Jamal
author_sort Tougui, Ilias
collection PubMed
description OBJECTIVES: Parkinson’s disease (PD) is the second most common neurodegenerative disorder; it affects more than 10 million people worldwide. Detecting PD usually requires a professional assessment by an expert, and investigation of the voice as a biomarker of the disease could be effective in speeding up the diagnostic process. METHODS: We present our methodology in which we distinguish PD patients from healthy controls (HC) using a large sample of 18,210 smartphone recordings. Those recordings were processed by an audio processing technique to create a final dataset of 80,594 instances and 138 features from the time, frequency, and cepstral domains. This dataset was preprocessed and normalized to create baseline machine-learning models using four classifiers, namely, linear support vector machine, K-nearest neighbor, random forest, and extreme gradient boosting (XGBoost). We divided our dataset into training and held-out test sets. Then we used stratified 5-fold cross-validation and four performance measures: accuracy, sensitivity, specificity, and F1-score to assess the performance of the models. We applied two feature selection methods, analysis of variance (ANOVA) and least absolute shrinkage and selection operator (LASSO), to reduce the dimensionality of the dataset by selecting the best subset of features that maximizes the performance of the classifiers. RESULTS: LASSO outperformed ANOVA with almost the same number of features. With 33 features, XGBoost achieved a maximum accuracy of 95.31% on training data, and 95.78% by predicting unseen data. CONCLUSIONS: Developing a smartphone-based system that implements machine-learning techniques is an effective way to diagnose PD using the voice as a biomarker.
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spelling pubmed-76748192020-11-19 Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease Tougui, Ilias Jilbab, Abdelilah El Mhamdi, Jamal Healthc Inform Res Original Article OBJECTIVES: Parkinson’s disease (PD) is the second most common neurodegenerative disorder; it affects more than 10 million people worldwide. Detecting PD usually requires a professional assessment by an expert, and investigation of the voice as a biomarker of the disease could be effective in speeding up the diagnostic process. METHODS: We present our methodology in which we distinguish PD patients from healthy controls (HC) using a large sample of 18,210 smartphone recordings. Those recordings were processed by an audio processing technique to create a final dataset of 80,594 instances and 138 features from the time, frequency, and cepstral domains. This dataset was preprocessed and normalized to create baseline machine-learning models using four classifiers, namely, linear support vector machine, K-nearest neighbor, random forest, and extreme gradient boosting (XGBoost). We divided our dataset into training and held-out test sets. Then we used stratified 5-fold cross-validation and four performance measures: accuracy, sensitivity, specificity, and F1-score to assess the performance of the models. We applied two feature selection methods, analysis of variance (ANOVA) and least absolute shrinkage and selection operator (LASSO), to reduce the dimensionality of the dataset by selecting the best subset of features that maximizes the performance of the classifiers. RESULTS: LASSO outperformed ANOVA with almost the same number of features. With 33 features, XGBoost achieved a maximum accuracy of 95.31% on training data, and 95.78% by predicting unseen data. CONCLUSIONS: Developing a smartphone-based system that implements machine-learning techniques is an effective way to diagnose PD using the voice as a biomarker. Korean Society of Medical Informatics 2020-10 2020-10-31 /pmc/articles/PMC7674819/ /pubmed/33190461 http://dx.doi.org/10.4258/hir.2020.26.4.274 Text en © 2020 The Korean Society of Medical Informatics This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tougui, Ilias
Jilbab, Abdelilah
El Mhamdi, Jamal
Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title_full Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title_fullStr Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title_full_unstemmed Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title_short Analysis of Smartphone Recordings in Time, Frequency, and Cepstral Domains to Classify Parkinson’s Disease
title_sort analysis of smartphone recordings in time, frequency, and cepstral domains to classify parkinson’s disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674819/
https://www.ncbi.nlm.nih.gov/pubmed/33190461
http://dx.doi.org/10.4258/hir.2020.26.4.274
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