Cargando…
Restricted language access during childhood affects adult brain structure in selective language regions
Due to the ubiquitous nature of language in the environment of infants, how it affects the anatomical structure of the brain language system over the lifespan is not well understood. In this study, we investigated the effects of early language experience on the adult brain by examining anatomical fe...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963327/ https://www.ncbi.nlm.nih.gov/pubmed/36745780 http://dx.doi.org/10.1073/pnas.2215423120 |
_version_ | 1784896225922777088 |
---|---|
author | Cheng, Qi Roth, Austin Halgren, Eric Klein, Denise Chen, Jen-Kai Mayberry, Rachel I. |
author_facet | Cheng, Qi Roth, Austin Halgren, Eric Klein, Denise Chen, Jen-Kai Mayberry, Rachel I. |
author_sort | Cheng, Qi |
collection | PubMed |
description | Due to the ubiquitous nature of language in the environment of infants, how it affects the anatomical structure of the brain language system over the lifespan is not well understood. In this study, we investigated the effects of early language experience on the adult brain by examining anatomical features of individuals born deaf with typical or restricted language experience in early childhood. Twenty-two deaf adults whose primary language was American Sign Language and were first immersed in it at ages ranging from birth to 14 y participated. The control group was 21 hearing non-signers. We acquired T1-weighted magnetic resonance images and used FreeSurfer [B. Fischl, Neuroimage 62, 774–781(2012)] to reconstruct the brain surface. Using an a priori regions of interest (ROI) approach, we identified 17 language and 19 somatomotor ROIs in each hemisphere from the Human Connectome Project parcellation map [M. F. Glasser et al., Nature 536, 171–178 (2016)]. Restricted language experience in early childhood was associated with negative changes in adjusted grey matter volume and/or cortical thickness in bilateral fronto-temporal regions. No evidence of anatomical differences was observed in any of these regions when deaf signers with infant sign language experience were compared with hearing speakers with infant spoken language experience, showing that the effects of early language experience on the brain language system are supramodal. |
format | Online Article Text |
id | pubmed-9963327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99633272023-02-26 Restricted language access during childhood affects adult brain structure in selective language regions Cheng, Qi Roth, Austin Halgren, Eric Klein, Denise Chen, Jen-Kai Mayberry, Rachel I. Proc Natl Acad Sci U S A Social Sciences Due to the ubiquitous nature of language in the environment of infants, how it affects the anatomical structure of the brain language system over the lifespan is not well understood. In this study, we investigated the effects of early language experience on the adult brain by examining anatomical features of individuals born deaf with typical or restricted language experience in early childhood. Twenty-two deaf adults whose primary language was American Sign Language and were first immersed in it at ages ranging from birth to 14 y participated. The control group was 21 hearing non-signers. We acquired T1-weighted magnetic resonance images and used FreeSurfer [B. Fischl, Neuroimage 62, 774–781(2012)] to reconstruct the brain surface. Using an a priori regions of interest (ROI) approach, we identified 17 language and 19 somatomotor ROIs in each hemisphere from the Human Connectome Project parcellation map [M. F. Glasser et al., Nature 536, 171–178 (2016)]. Restricted language experience in early childhood was associated with negative changes in adjusted grey matter volume and/or cortical thickness in bilateral fronto-temporal regions. No evidence of anatomical differences was observed in any of these regions when deaf signers with infant sign language experience were compared with hearing speakers with infant spoken language experience, showing that the effects of early language experience on the brain language system are supramodal. National Academy of Sciences 2023-02-06 2023-02-14 /pmc/articles/PMC9963327/ /pubmed/36745780 http://dx.doi.org/10.1073/pnas.2215423120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Social Sciences Cheng, Qi Roth, Austin Halgren, Eric Klein, Denise Chen, Jen-Kai Mayberry, Rachel I. Restricted language access during childhood affects adult brain structure in selective language regions |
title | Restricted language access during childhood affects adult brain structure in selective language regions |
title_full | Restricted language access during childhood affects adult brain structure in selective language regions |
title_fullStr | Restricted language access during childhood affects adult brain structure in selective language regions |
title_full_unstemmed | Restricted language access during childhood affects adult brain structure in selective language regions |
title_short | Restricted language access during childhood affects adult brain structure in selective language regions |
title_sort | restricted language access during childhood affects adult brain structure in selective language regions |
topic | Social Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963327/ https://www.ncbi.nlm.nih.gov/pubmed/36745780 http://dx.doi.org/10.1073/pnas.2215423120 |
work_keys_str_mv | AT chengqi restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions AT rothaustin restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions AT halgreneric restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions AT kleindenise restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions AT chenjenkai restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions AT mayberryracheli restrictedlanguageaccessduringchildhoodaffectsadultbrainstructureinselectivelanguageregions |