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Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease

BACKGROUND: Although increased nasality can originate from basal ganglia dysfunction, data regarding hypernasality in Parkinson’s disease (PD) and Huntington’s disease (HD) are very sparse. The aim of the current study was to analyze acoustic and perceptual correlates of velopharyngeal seal closure...

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Autores principales: Novotný, Michal, Rusz, Jan, Čmejla, Roman, Růžičková, Hana, Klempíř, Jiří, Růžička, Evžen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047145/
https://www.ncbi.nlm.nih.gov/pubmed/27703866
http://dx.doi.org/10.7717/peerj.2530
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author Novotný, Michal
Rusz, Jan
Čmejla, Roman
Růžičková, Hana
Klempíř, Jiří
Růžička, Evžen
author_facet Novotný, Michal
Rusz, Jan
Čmejla, Roman
Růžičková, Hana
Klempíř, Jiří
Růžička, Evžen
author_sort Novotný, Michal
collection PubMed
description BACKGROUND: Although increased nasality can originate from basal ganglia dysfunction, data regarding hypernasality in Parkinson’s disease (PD) and Huntington’s disease (HD) are very sparse. The aim of the current study was to analyze acoustic and perceptual correlates of velopharyngeal seal closure in 37 PD and 37 HD participants in comparison to 37 healthy control speakers. METHODS: Acoustical analysis was based on sustained phonation of the vowel /i/ and perceptual analysis was based on monologue. Perceptual analysis was performed by 10 raters using The Great Ormond Street Speech Assessment ’98. Acoustic parameters related to changes in a 1/3-octave band centered on 1 kHz were proposed to reflect nasality level and behavior through utterance. RESULTS: Perceptual analysis showed the occurrence of mild to moderate hypernasality in 65% of PD, 89% of HD and 22% of control speakers. Based on acoustic analyses, 27% of PD, 54% of HD and 19% of control speakers showed an increased occurrence of hypernasality. In addition, 78% of HD patients demonstrated a high occurrence of intermittent hypernasality. Further results indicated relationships between the acoustic parameter representing fluctuation of nasality and perceptual assessment (r = 0.51, p < 0.001) as well as the Unified Huntington Disease Rating Scale chorea composite subscore (r = 0.42, p = 0.01). CONCLUSIONS: In conclusion the acoustic assessment showed that abnormal nasality was not a common feature of PD, whereas patients with HD manifested intermittent hypernasality associated with chorea.
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spelling pubmed-50471452016-10-04 Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease Novotný, Michal Rusz, Jan Čmejla, Roman Růžičková, Hana Klempíř, Jiří Růžička, Evžen PeerJ Neuroscience BACKGROUND: Although increased nasality can originate from basal ganglia dysfunction, data regarding hypernasality in Parkinson’s disease (PD) and Huntington’s disease (HD) are very sparse. The aim of the current study was to analyze acoustic and perceptual correlates of velopharyngeal seal closure in 37 PD and 37 HD participants in comparison to 37 healthy control speakers. METHODS: Acoustical analysis was based on sustained phonation of the vowel /i/ and perceptual analysis was based on monologue. Perceptual analysis was performed by 10 raters using The Great Ormond Street Speech Assessment ’98. Acoustic parameters related to changes in a 1/3-octave band centered on 1 kHz were proposed to reflect nasality level and behavior through utterance. RESULTS: Perceptual analysis showed the occurrence of mild to moderate hypernasality in 65% of PD, 89% of HD and 22% of control speakers. Based on acoustic analyses, 27% of PD, 54% of HD and 19% of control speakers showed an increased occurrence of hypernasality. In addition, 78% of HD patients demonstrated a high occurrence of intermittent hypernasality. Further results indicated relationships between the acoustic parameter representing fluctuation of nasality and perceptual assessment (r = 0.51, p < 0.001) as well as the Unified Huntington Disease Rating Scale chorea composite subscore (r = 0.42, p = 0.01). CONCLUSIONS: In conclusion the acoustic assessment showed that abnormal nasality was not a common feature of PD, whereas patients with HD manifested intermittent hypernasality associated with chorea. PeerJ Inc. 2016-09-29 /pmc/articles/PMC5047145/ /pubmed/27703866 http://dx.doi.org/10.7717/peerj.2530 Text en ©2016 Novotný et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Neuroscience
Novotný, Michal
Rusz, Jan
Čmejla, Roman
Růžičková, Hana
Klempíř, Jiří
Růžička, Evžen
Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title_full Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title_fullStr Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title_full_unstemmed Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title_short Hypernasality associated with basal ganglia dysfunction: evidence from Parkinson’s disease and Huntington’s disease
title_sort hypernasality associated with basal ganglia dysfunction: evidence from parkinson’s disease and huntington’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047145/
https://www.ncbi.nlm.nih.gov/pubmed/27703866
http://dx.doi.org/10.7717/peerj.2530
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