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Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease

In this paper, we have investigated the differences in the voices of Parkinson’s disease (PD) and age-matched control (CO) subjects when uttering three phonemes using two complexity measures: fractal dimension (FD) and normalised mutual information (NMI). Three sustained phonetic voice recordings, /...

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Autores principales: Viswanathan, Rekha, Arjunan, Sridhar P., Bingham, Adrian, Jelfs, Beth, Kempster, Peter, Raghav, Sanjay, Kumar, Dinesh K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168233/
https://www.ncbi.nlm.nih.gov/pubmed/31861890
http://dx.doi.org/10.3390/bios10010001
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author Viswanathan, Rekha
Arjunan, Sridhar P.
Bingham, Adrian
Jelfs, Beth
Kempster, Peter
Raghav, Sanjay
Kumar, Dinesh K.
author_facet Viswanathan, Rekha
Arjunan, Sridhar P.
Bingham, Adrian
Jelfs, Beth
Kempster, Peter
Raghav, Sanjay
Kumar, Dinesh K.
author_sort Viswanathan, Rekha
collection PubMed
description In this paper, we have investigated the differences in the voices of Parkinson’s disease (PD) and age-matched control (CO) subjects when uttering three phonemes using two complexity measures: fractal dimension (FD) and normalised mutual information (NMI). Three sustained phonetic voice recordings, /a/, /u/ and /m/, from 22 CO (mean age = 66.91) and 24 PD (mean age = 71.83) participants were analysed. FD was first computed for PD and CO voice recordings, followed by the computation of NMI between the test groups: PD–CO, PD–PD and CO–CO. Four features reported in the literature—normalised pitch period entropy (Norm. PPE), glottal-to-noise excitation ratio (GNE), detrended fluctuation analysis (DFA) and glottal closing quotient (ClQ)—were also computed for comparison with the proposed complexity measures. The statistical significance of the features was tested using a one-way ANOVA test. Support vector machine (SVM) with a linear kernel was used to classify the test groups, using a leave-one-out validation method. The results showed that PD voice recordings had lower FD compared to CO (p < 0.008). It was also observed that the average NMI between CO voice recordings was significantly lower compared with the CO–PD and PD–PD groups (p < 0.036) for the three phonetic sounds. The average NMI and FD demonstrated higher accuracy (>80%) in differentiating the test groups compared with other speech feature-based classifications. This study has demonstrated that the voices of PD patients has reduced FD, and NMI between voice recordings of PD–CO and PD–PD is higher compared with CO–CO. This suggests that the use of NMI obtained from the sample voice, when paired with known groups of CO and PD, can be used to identify PD voices. These findings could have applications for population screening.
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spelling pubmed-71682332020-04-22 Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease Viswanathan, Rekha Arjunan, Sridhar P. Bingham, Adrian Jelfs, Beth Kempster, Peter Raghav, Sanjay Kumar, Dinesh K. Biosensors (Basel) Article In this paper, we have investigated the differences in the voices of Parkinson’s disease (PD) and age-matched control (CO) subjects when uttering three phonemes using two complexity measures: fractal dimension (FD) and normalised mutual information (NMI). Three sustained phonetic voice recordings, /a/, /u/ and /m/, from 22 CO (mean age = 66.91) and 24 PD (mean age = 71.83) participants were analysed. FD was first computed for PD and CO voice recordings, followed by the computation of NMI between the test groups: PD–CO, PD–PD and CO–CO. Four features reported in the literature—normalised pitch period entropy (Norm. PPE), glottal-to-noise excitation ratio (GNE), detrended fluctuation analysis (DFA) and glottal closing quotient (ClQ)—were also computed for comparison with the proposed complexity measures. The statistical significance of the features was tested using a one-way ANOVA test. Support vector machine (SVM) with a linear kernel was used to classify the test groups, using a leave-one-out validation method. The results showed that PD voice recordings had lower FD compared to CO (p < 0.008). It was also observed that the average NMI between CO voice recordings was significantly lower compared with the CO–PD and PD–PD groups (p < 0.036) for the three phonetic sounds. The average NMI and FD demonstrated higher accuracy (>80%) in differentiating the test groups compared with other speech feature-based classifications. This study has demonstrated that the voices of PD patients has reduced FD, and NMI between voice recordings of PD–CO and PD–PD is higher compared with CO–CO. This suggests that the use of NMI obtained from the sample voice, when paired with known groups of CO and PD, can be used to identify PD voices. These findings could have applications for population screening. MDPI 2019-12-20 /pmc/articles/PMC7168233/ /pubmed/31861890 http://dx.doi.org/10.3390/bios10010001 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Viswanathan, Rekha
Arjunan, Sridhar P.
Bingham, Adrian
Jelfs, Beth
Kempster, Peter
Raghav, Sanjay
Kumar, Dinesh K.
Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title_full Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title_fullStr Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title_full_unstemmed Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title_short Complexity Measures of Voice Recordings as a Discriminative Tool for Parkinson’s Disease
title_sort complexity measures of voice recordings as a discriminative tool for parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168233/
https://www.ncbi.nlm.nih.gov/pubmed/31861890
http://dx.doi.org/10.3390/bios10010001
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