Cargando…

A neurophysiological model of speech production deficits in fragile X syndrome

Fragile X syndrome is the most common inherited intellectual disability and monogenic cause of autism spectrum disorder. Expressive language deficits, especially in speech production, are nearly ubiquitous among individuals with fragile X, but understanding of the neurological bases for these defici...

Descripción completa

Detalles Bibliográficos
Autores principales: Schmitt, Lauren M, Wang, Jun, Pedapati, Ernest V, Thurman, Angela John, Abbeduto, Leonard, Erickson, Craig A, Sweeney, John A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425415/
https://www.ncbi.nlm.nih.gov/pubmed/32924010
http://dx.doi.org/10.1093/braincomms/fcz042
_version_ 1783570488870567936
author Schmitt, Lauren M
Wang, Jun
Pedapati, Ernest V
Thurman, Angela John
Abbeduto, Leonard
Erickson, Craig A
Sweeney, John A
author_facet Schmitt, Lauren M
Wang, Jun
Pedapati, Ernest V
Thurman, Angela John
Abbeduto, Leonard
Erickson, Craig A
Sweeney, John A
author_sort Schmitt, Lauren M
collection PubMed
description Fragile X syndrome is the most common inherited intellectual disability and monogenic cause of autism spectrum disorder. Expressive language deficits, especially in speech production, are nearly ubiquitous among individuals with fragile X, but understanding of the neurological bases for these deficits remains limited. Speech production depends on feedforward control and the synchronization of neural oscillations between speech-related areas of frontal cortex and auditory areas of temporal cortex. Interaction in this circuitry allows the corollary discharge of intended speech generated from an efference copy of speech commands to be compared against actual speech sounds, which is critical for making adaptive adjustments to optimize future speech. We aimed to determine whether alterations in coherence between frontal and temporal cortices prior to speech production are present in individuals with fragile X and whether they relate to expressive language dysfunction. Twenty-one participants with full-mutation fragile X syndrome (aged 7–55 years, eight females) and 20 healthy controls (matched on age and sex) completed a talk/listen paradigm during high-density EEG recordings. During the talk task, participants repeated pronounced short vocalizations of ‘Ah’ every 1–2 s for a total of 180 s. During the listen task, participants passively listened to their recordings from the talk task. We compared pre-speech event-related potential activity, N1 suppression to speech sounds, single trial gamma power and fronto-temporal coherence between groups during these tasks and examined their relation to performance during a naturalistic language task. Prior to speech production, fragile X participants showed reduced pre-speech negativity, reduced fronto-temporal connectivity and greater frontal gamma power compared to controls. N1 suppression during self-generated speech did not differ between groups. Reduced pre-speech activity and increased frontal gamma power prior to speech production were related to less intelligible speech as well as broader social communication deficits in fragile X syndrome. Our findings indicate that coordinated pre-speech activity between frontal and temporal cortices is disrupted in individuals with fragile X in a clinically relevant way and represents a mechanism contributing to prominent speech production problems in the disorder.
format Online
Article
Text
id pubmed-7425415
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-74254152020-09-17 A neurophysiological model of speech production deficits in fragile X syndrome Schmitt, Lauren M Wang, Jun Pedapati, Ernest V Thurman, Angela John Abbeduto, Leonard Erickson, Craig A Sweeney, John A Brain Commun Original Article Fragile X syndrome is the most common inherited intellectual disability and monogenic cause of autism spectrum disorder. Expressive language deficits, especially in speech production, are nearly ubiquitous among individuals with fragile X, but understanding of the neurological bases for these deficits remains limited. Speech production depends on feedforward control and the synchronization of neural oscillations between speech-related areas of frontal cortex and auditory areas of temporal cortex. Interaction in this circuitry allows the corollary discharge of intended speech generated from an efference copy of speech commands to be compared against actual speech sounds, which is critical for making adaptive adjustments to optimize future speech. We aimed to determine whether alterations in coherence between frontal and temporal cortices prior to speech production are present in individuals with fragile X and whether they relate to expressive language dysfunction. Twenty-one participants with full-mutation fragile X syndrome (aged 7–55 years, eight females) and 20 healthy controls (matched on age and sex) completed a talk/listen paradigm during high-density EEG recordings. During the talk task, participants repeated pronounced short vocalizations of ‘Ah’ every 1–2 s for a total of 180 s. During the listen task, participants passively listened to their recordings from the talk task. We compared pre-speech event-related potential activity, N1 suppression to speech sounds, single trial gamma power and fronto-temporal coherence between groups during these tasks and examined their relation to performance during a naturalistic language task. Prior to speech production, fragile X participants showed reduced pre-speech negativity, reduced fronto-temporal connectivity and greater frontal gamma power compared to controls. N1 suppression during self-generated speech did not differ between groups. Reduced pre-speech activity and increased frontal gamma power prior to speech production were related to less intelligible speech as well as broader social communication deficits in fragile X syndrome. Our findings indicate that coordinated pre-speech activity between frontal and temporal cortices is disrupted in individuals with fragile X in a clinically relevant way and represents a mechanism contributing to prominent speech production problems in the disorder. Oxford University Press 2019-12-09 /pmc/articles/PMC7425415/ /pubmed/32924010 http://dx.doi.org/10.1093/braincomms/fcz042 Text en © The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ 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 non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Schmitt, Lauren M
Wang, Jun
Pedapati, Ernest V
Thurman, Angela John
Abbeduto, Leonard
Erickson, Craig A
Sweeney, John A
A neurophysiological model of speech production deficits in fragile X syndrome
title A neurophysiological model of speech production deficits in fragile X syndrome
title_full A neurophysiological model of speech production deficits in fragile X syndrome
title_fullStr A neurophysiological model of speech production deficits in fragile X syndrome
title_full_unstemmed A neurophysiological model of speech production deficits in fragile X syndrome
title_short A neurophysiological model of speech production deficits in fragile X syndrome
title_sort neurophysiological model of speech production deficits in fragile x syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425415/
https://www.ncbi.nlm.nih.gov/pubmed/32924010
http://dx.doi.org/10.1093/braincomms/fcz042
work_keys_str_mv AT schmittlaurenm aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT wangjun aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT pedapatiernestv aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT thurmanangelajohn aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT abbedutoleonard aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT ericksoncraiga aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT sweeneyjohna aneurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT schmittlaurenm neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT wangjun neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT pedapatiernestv neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT thurmanangelajohn neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT abbedutoleonard neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT ericksoncraiga neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome
AT sweeneyjohna neurophysiologicalmodelofspeechproductiondeficitsinfragilexsyndrome