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Multilayer network associations between the exposome and childhood brain development
Growing up in a high poverty neighborhood is associated with elevated risk for academic challenges and health problems. Here, we take a data-driven approach to exploring how measures of children’s environments relate to the development of their brain structure and function in a community sample of c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634748/ https://www.ncbi.nlm.nih.gov/pubmed/37961103 http://dx.doi.org/10.1101/2023.10.23.563611 |
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author | Simpson-Kent, Ivan L. Gataviņš, Mārtiņš M. Tooley, Ursula A. Boroshok, Austin L. McDermott, Cassidy L. Park, Anne T. Delgado Reyes, Lourdes Bathelt, Joe Tisdall, M. Dylan Mackey, Allyson P. |
author_facet | Simpson-Kent, Ivan L. Gataviņš, Mārtiņš M. Tooley, Ursula A. Boroshok, Austin L. McDermott, Cassidy L. Park, Anne T. Delgado Reyes, Lourdes Bathelt, Joe Tisdall, M. Dylan Mackey, Allyson P. |
author_sort | Simpson-Kent, Ivan L. |
collection | PubMed |
description | Growing up in a high poverty neighborhood is associated with elevated risk for academic challenges and health problems. Here, we take a data-driven approach to exploring how measures of children’s environments relate to the development of their brain structure and function in a community sample of children between the ages of 4 and 10 years. We constructed exposomes including measures of family socioeconomic status, children’s exposure to adversity, and geocoded measures of neighborhood socioeconomic status, crime, and environmental toxins. We connected the exposome to two structural measures (cortical thickness and surface area, n = 170) and two functional measures (participation coefficient and clustering coefficient, n = 130). We found dense connections within exposome and brain layers and sparse connections between exposome and brain layers. Lower family income was associated with thinner visual cortex, consistent with the theory that accelerated development is detectable in early-developing regions. Greater neighborhood incidence of high blood lead levels was associated with greater segregation of the default mode network, consistent with evidence that toxins are deposited into the brain along the midline. Our study demonstrates the utility of multilayer network analysis to bridge environmental and neural explanatory levels to better understand the complexity of child development. |
format | Online Article Text |
id | pubmed-10634748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106347482023-11-13 Multilayer network associations between the exposome and childhood brain development Simpson-Kent, Ivan L. Gataviņš, Mārtiņš M. Tooley, Ursula A. Boroshok, Austin L. McDermott, Cassidy L. Park, Anne T. Delgado Reyes, Lourdes Bathelt, Joe Tisdall, M. Dylan Mackey, Allyson P. bioRxiv Article Growing up in a high poverty neighborhood is associated with elevated risk for academic challenges and health problems. Here, we take a data-driven approach to exploring how measures of children’s environments relate to the development of their brain structure and function in a community sample of children between the ages of 4 and 10 years. We constructed exposomes including measures of family socioeconomic status, children’s exposure to adversity, and geocoded measures of neighborhood socioeconomic status, crime, and environmental toxins. We connected the exposome to two structural measures (cortical thickness and surface area, n = 170) and two functional measures (participation coefficient and clustering coefficient, n = 130). We found dense connections within exposome and brain layers and sparse connections between exposome and brain layers. Lower family income was associated with thinner visual cortex, consistent with the theory that accelerated development is detectable in early-developing regions. Greater neighborhood incidence of high blood lead levels was associated with greater segregation of the default mode network, consistent with evidence that toxins are deposited into the brain along the midline. Our study demonstrates the utility of multilayer network analysis to bridge environmental and neural explanatory levels to better understand the complexity of child development. Cold Spring Harbor Laboratory 2023-10-25 /pmc/articles/PMC10634748/ /pubmed/37961103 http://dx.doi.org/10.1101/2023.10.23.563611 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Simpson-Kent, Ivan L. Gataviņš, Mārtiņš M. Tooley, Ursula A. Boroshok, Austin L. McDermott, Cassidy L. Park, Anne T. Delgado Reyes, Lourdes Bathelt, Joe Tisdall, M. Dylan Mackey, Allyson P. Multilayer network associations between the exposome and childhood brain development |
title | Multilayer network associations between the exposome and childhood brain development |
title_full | Multilayer network associations between the exposome and childhood brain development |
title_fullStr | Multilayer network associations between the exposome and childhood brain development |
title_full_unstemmed | Multilayer network associations between the exposome and childhood brain development |
title_short | Multilayer network associations between the exposome and childhood brain development |
title_sort | multilayer network associations between the exposome and childhood brain development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634748/ https://www.ncbi.nlm.nih.gov/pubmed/37961103 http://dx.doi.org/10.1101/2023.10.23.563611 |
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