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Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years

Low childhood socioeconomic status (SES) predisposes individuals to altered trajectories of brain development and increased rates of mental illness. Brain connectivity at birth is associated with psychiatric outcomes. We sought to investigate whether SES at birth is associated with neonatal brain co...

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Autores principales: Ramphal, Bruce, Whalen, Diana J., Kenley, Jeanette K., Yu, Qiongru, Smyser, Christopher D., Rogers, Cynthia E., Sylvester, Chad M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451824/
https://www.ncbi.nlm.nih.gov/pubmed/32823180
http://dx.doi.org/10.1016/j.dcn.2020.100811
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author Ramphal, Bruce
Whalen, Diana J.
Kenley, Jeanette K.
Yu, Qiongru
Smyser, Christopher D.
Rogers, Cynthia E.
Sylvester, Chad M.
author_facet Ramphal, Bruce
Whalen, Diana J.
Kenley, Jeanette K.
Yu, Qiongru
Smyser, Christopher D.
Rogers, Cynthia E.
Sylvester, Chad M.
author_sort Ramphal, Bruce
collection PubMed
description Low childhood socioeconomic status (SES) predisposes individuals to altered trajectories of brain development and increased rates of mental illness. Brain connectivity at birth is associated with psychiatric outcomes. We sought to investigate whether SES at birth is associated with neonatal brain connectivity and if these differences account for socioeconomic disparities in infant symptoms at age 2 years that are predictive of psychopathology. Resting state functional MRI was performed on 75 full-term and 37 term-equivalent preterm newborns (n = 112). SES was characterized by insurance type, the Area Deprivation Index, and a composite score. Seed-based voxelwise linear regression related SES to whole-brain functional connectivity of five brain regions representing functional networks implicated in psychiatric illnesses and affected by socioeconomic disadvantage: striatum, medial prefrontal cortex (mPFC), ventrolateral prefrontal cortex (vlPFC), and dorsal anterior cingulate cortex. Lower SES was associated with differences in striatum and vlPFC connectivity. Striatum connectivity with frontopolar and medial PFC mediated the relationship between SES and behavioral inhibition at age 2 measured by the Infant-Toddler Social Emotional Assessment (n = 46). Striatum-frontopolar connectivity mediated the relationship between SES and externalizing symptoms. These results, convergent across three SES metrics, suggest that neurodevelopmental trajectories linking SES and mental illness may begin as early as birth.
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spelling pubmed-74518242020-09-02 Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years Ramphal, Bruce Whalen, Diana J. Kenley, Jeanette K. Yu, Qiongru Smyser, Christopher D. Rogers, Cynthia E. Sylvester, Chad M. Dev Cogn Neurosci Articles from the Special Issue from the Flux Congress 2019: Cutting edge approaches to developmental neuroscience; Edited by Deanna Barch. Low childhood socioeconomic status (SES) predisposes individuals to altered trajectories of brain development and increased rates of mental illness. Brain connectivity at birth is associated with psychiatric outcomes. We sought to investigate whether SES at birth is associated with neonatal brain connectivity and if these differences account for socioeconomic disparities in infant symptoms at age 2 years that are predictive of psychopathology. Resting state functional MRI was performed on 75 full-term and 37 term-equivalent preterm newborns (n = 112). SES was characterized by insurance type, the Area Deprivation Index, and a composite score. Seed-based voxelwise linear regression related SES to whole-brain functional connectivity of five brain regions representing functional networks implicated in psychiatric illnesses and affected by socioeconomic disadvantage: striatum, medial prefrontal cortex (mPFC), ventrolateral prefrontal cortex (vlPFC), and dorsal anterior cingulate cortex. Lower SES was associated with differences in striatum and vlPFC connectivity. Striatum connectivity with frontopolar and medial PFC mediated the relationship between SES and behavioral inhibition at age 2 measured by the Infant-Toddler Social Emotional Assessment (n = 46). Striatum-frontopolar connectivity mediated the relationship between SES and externalizing symptoms. These results, convergent across three SES metrics, suggest that neurodevelopmental trajectories linking SES and mental illness may begin as early as birth. Elsevier 2020-06-30 /pmc/articles/PMC7451824/ /pubmed/32823180 http://dx.doi.org/10.1016/j.dcn.2020.100811 Text en © 2020 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles from the Special Issue from the Flux Congress 2019: Cutting edge approaches to developmental neuroscience; Edited by Deanna Barch.
Ramphal, Bruce
Whalen, Diana J.
Kenley, Jeanette K.
Yu, Qiongru
Smyser, Christopher D.
Rogers, Cynthia E.
Sylvester, Chad M.
Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title_full Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title_fullStr Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title_full_unstemmed Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title_short Brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
title_sort brain connectivity and socioeconomic status at birth and externalizing symptoms at age 2 years
topic Articles from the Special Issue from the Flux Congress 2019: Cutting edge approaches to developmental neuroscience; Edited by Deanna Barch.
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451824/
https://www.ncbi.nlm.nih.gov/pubmed/32823180
http://dx.doi.org/10.1016/j.dcn.2020.100811
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