Cargando…

The impact of early language exposure on the neural system supporting language in deaf and hearing adults

Deaf late signers provide a unique perspective on the impact of impoverished early language exposure on the neurobiology of language: insights that cannot be gained from research with hearing people alone. Here we contrast the effect of age of sign language acquisition in hearing and congenitally de...

Descripción completa

Detalles Bibliográficos
Autores principales: Twomey, Tae, Price, Cathy J., Waters, Dafydd, MacSweeney, Mairéad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985620/
https://www.ncbi.nlm.nih.gov/pubmed/31857205
http://dx.doi.org/10.1016/j.neuroimage.2019.116411
_version_ 1783668285557964800
author Twomey, Tae
Price, Cathy J.
Waters, Dafydd
MacSweeney, Mairéad
author_facet Twomey, Tae
Price, Cathy J.
Waters, Dafydd
MacSweeney, Mairéad
author_sort Twomey, Tae
collection PubMed
description Deaf late signers provide a unique perspective on the impact of impoverished early language exposure on the neurobiology of language: insights that cannot be gained from research with hearing people alone. Here we contrast the effect of age of sign language acquisition in hearing and congenitally deaf adults to examine the potential impact of impoverished early language exposure on the neural systems supporting a language learnt later in life. We collected fMRI data from deaf and hearing proficient users (N ​= ​52) of British Sign Language (BSL), who learnt BSL either early (native) or late (after the age of 15 years) whilst they watched BSL sentences or strings of meaningless nonsense signs. There was a main effect of age of sign language acquisition (late ​> ​early) across deaf and hearing signers in the occipital segment of the left intraparietal sulcus. This finding suggests that late learners of sign language may rely on visual processing more than early learners, when processing both linguistic and nonsense sign input – regardless of hearing status. Region-of-interest analyses in the posterior superior temporal cortices (STC) showed an effect of age of sign language acquisition that was specific to deaf signers. In the left posterior STC, activation in response to signed sentences was greater in deaf early signers than deaf late signers. Importantly, responses in the left posterior STC in hearing early and late signers did not differ, and were similar to those observed in deaf early signers. These data lend further support to the argument that robust early language experience, whether signed or spoken, is necessary for left posterior STC to show a ‘native-like’ response to a later learnt language.
format Online
Article
Text
id pubmed-7985620
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Academic Press
record_format MEDLINE/PubMed
spelling pubmed-79856202021-03-24 The impact of early language exposure on the neural system supporting language in deaf and hearing adults Twomey, Tae Price, Cathy J. Waters, Dafydd MacSweeney, Mairéad Neuroimage Article Deaf late signers provide a unique perspective on the impact of impoverished early language exposure on the neurobiology of language: insights that cannot be gained from research with hearing people alone. Here we contrast the effect of age of sign language acquisition in hearing and congenitally deaf adults to examine the potential impact of impoverished early language exposure on the neural systems supporting a language learnt later in life. We collected fMRI data from deaf and hearing proficient users (N ​= ​52) of British Sign Language (BSL), who learnt BSL either early (native) or late (after the age of 15 years) whilst they watched BSL sentences or strings of meaningless nonsense signs. There was a main effect of age of sign language acquisition (late ​> ​early) across deaf and hearing signers in the occipital segment of the left intraparietal sulcus. This finding suggests that late learners of sign language may rely on visual processing more than early learners, when processing both linguistic and nonsense sign input – regardless of hearing status. Region-of-interest analyses in the posterior superior temporal cortices (STC) showed an effect of age of sign language acquisition that was specific to deaf signers. In the left posterior STC, activation in response to signed sentences was greater in deaf early signers than deaf late signers. Importantly, responses in the left posterior STC in hearing early and late signers did not differ, and were similar to those observed in deaf early signers. These data lend further support to the argument that robust early language experience, whether signed or spoken, is necessary for left posterior STC to show a ‘native-like’ response to a later learnt language. Academic Press 2020-04-01 /pmc/articles/PMC7985620/ /pubmed/31857205 http://dx.doi.org/10.1016/j.neuroimage.2019.116411 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Twomey, Tae
Price, Cathy J.
Waters, Dafydd
MacSweeney, Mairéad
The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title_full The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title_fullStr The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title_full_unstemmed The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title_short The impact of early language exposure on the neural system supporting language in deaf and hearing adults
title_sort impact of early language exposure on the neural system supporting language in deaf and hearing adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985620/
https://www.ncbi.nlm.nih.gov/pubmed/31857205
http://dx.doi.org/10.1016/j.neuroimage.2019.116411
work_keys_str_mv AT twomeytae theimpactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT pricecathyj theimpactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT watersdafydd theimpactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT macsweeneymairead theimpactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT twomeytae impactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT pricecathyj impactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT watersdafydd impactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults
AT macsweeneymairead impactofearlylanguageexposureontheneuralsystemsupportinglanguageindeafandhearingadults