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Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions

Speech and motor deficits are highly prevalent (>70%) in individuals with the 600 kb BP4-BP5 16p11.2 deletion; however, the mechanisms that drive these deficits are unclear, limiting our ability to target interventions and advance treatment. This study examined fundamental aspects of speech motor...

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Autores principales: Demopoulos, Carly, Kothare, Hardik, Mizuiri, Danielle, Henderson-Sabes, Jennifer, Fregeau, Brieana, Tjernagel, Jennifer, Houde, John F., Sherr, Elliott H., Nagarajan, Srikantan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775320/
https://www.ncbi.nlm.nih.gov/pubmed/29352208
http://dx.doi.org/10.1038/s41598-018-19751-x
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author Demopoulos, Carly
Kothare, Hardik
Mizuiri, Danielle
Henderson-Sabes, Jennifer
Fregeau, Brieana
Tjernagel, Jennifer
Houde, John F.
Sherr, Elliott H.
Nagarajan, Srikantan S.
author_facet Demopoulos, Carly
Kothare, Hardik
Mizuiri, Danielle
Henderson-Sabes, Jennifer
Fregeau, Brieana
Tjernagel, Jennifer
Houde, John F.
Sherr, Elliott H.
Nagarajan, Srikantan S.
author_sort Demopoulos, Carly
collection PubMed
description Speech and motor deficits are highly prevalent (>70%) in individuals with the 600 kb BP4-BP5 16p11.2 deletion; however, the mechanisms that drive these deficits are unclear, limiting our ability to target interventions and advance treatment. This study examined fundamental aspects of speech motor control in participants with the 16p11.2 deletion. To assess capacity for control of voice, we examined how accurately and quickly subjects changed the pitch of their voice within a trial to correct for a transient perturbation of the pitch of their auditory feedback. When compared to controls, 16p11.2 deletion carriers show an over-exaggerated pitch compensation response to unpredictable mid-vocalization pitch perturbations. We also examined sensorimotor adaptation of speech by assessing how subjects learned to adapt their sustained productions of formants (speech spectral peak frequencies important for vowel identity), in response to consistent changes in their auditory feedback during vowel production. Deletion carriers show reduced sensorimotor adaptation to sustained vowel identity changes in auditory feedback. These results together suggest that 16p11.2 deletion carriers have fundamental impairments in the basic mechanisms of speech motor control and these impairments may partially explain the deficits in speech and language in these individuals.
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spelling pubmed-57753202018-01-26 Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions Demopoulos, Carly Kothare, Hardik Mizuiri, Danielle Henderson-Sabes, Jennifer Fregeau, Brieana Tjernagel, Jennifer Houde, John F. Sherr, Elliott H. Nagarajan, Srikantan S. Sci Rep Article Speech and motor deficits are highly prevalent (>70%) in individuals with the 600 kb BP4-BP5 16p11.2 deletion; however, the mechanisms that drive these deficits are unclear, limiting our ability to target interventions and advance treatment. This study examined fundamental aspects of speech motor control in participants with the 16p11.2 deletion. To assess capacity for control of voice, we examined how accurately and quickly subjects changed the pitch of their voice within a trial to correct for a transient perturbation of the pitch of their auditory feedback. When compared to controls, 16p11.2 deletion carriers show an over-exaggerated pitch compensation response to unpredictable mid-vocalization pitch perturbations. We also examined sensorimotor adaptation of speech by assessing how subjects learned to adapt their sustained productions of formants (speech spectral peak frequencies important for vowel identity), in response to consistent changes in their auditory feedback during vowel production. Deletion carriers show reduced sensorimotor adaptation to sustained vowel identity changes in auditory feedback. These results together suggest that 16p11.2 deletion carriers have fundamental impairments in the basic mechanisms of speech motor control and these impairments may partially explain the deficits in speech and language in these individuals. Nature Publishing Group UK 2018-01-19 /pmc/articles/PMC5775320/ /pubmed/29352208 http://dx.doi.org/10.1038/s41598-018-19751-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Demopoulos, Carly
Kothare, Hardik
Mizuiri, Danielle
Henderson-Sabes, Jennifer
Fregeau, Brieana
Tjernagel, Jennifer
Houde, John F.
Sherr, Elliott H.
Nagarajan, Srikantan S.
Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title_full Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title_fullStr Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title_full_unstemmed Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title_short Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions
title_sort abnormal speech motor control in individuals with 16p11.2 deletions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775320/
https://www.ncbi.nlm.nih.gov/pubmed/29352208
http://dx.doi.org/10.1038/s41598-018-19751-x
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