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Poverty from fetal life onward and child brain morphology
Poverty is a risk factor for impaired child development, an association possibly mediated by brain morphology. Previous studies lacked prospective poverty assessments during pregnancy and did not stratify by majority/minority status. We investigated the association of household poverty from fetal li...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9870876/ https://www.ncbi.nlm.nih.gov/pubmed/36690659 http://dx.doi.org/10.1038/s41598-023-28120-2 |
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author | Koyama, Yuna Hidalgo, Andrea P. Cortes Lacey, Rebecca E. White, Tonya Jansen, Pauline W. Fujiwara, Takeo Tiemeier, Henning |
author_facet | Koyama, Yuna Hidalgo, Andrea P. Cortes Lacey, Rebecca E. White, Tonya Jansen, Pauline W. Fujiwara, Takeo Tiemeier, Henning |
author_sort | Koyama, Yuna |
collection | PubMed |
description | Poverty is a risk factor for impaired child development, an association possibly mediated by brain morphology. Previous studies lacked prospective poverty assessments during pregnancy and did not stratify by majority/minority status. We investigated the association of household poverty from fetal life forward with brain morphological differences at age 10 years, in 2166 mother–child dyads. Overall, the results showed no associations between any poverty exposure early in life and brain volumes. However, there was the evidence of timing effects: children exposed to poverty in utero had smaller amygdala volumes (B = − 0.18, 95%CI − 0.30; − 0.07, p(FDR-adjusted) = 0.009). There were also differences in associations by majority/minority status (cerebral white matter: p for interaction = 0.04). Dutch children exposed to childhood poverty showed smaller cerebral white matter volumes than their control (B = − 0.26, 95%CI − 0.45; − 0.06, p(FDR-adjusted) = 0.035). This association was not observed in the minority population (B = − 0.05, 95%CI − 0.23; 0.12, p(FDR-adjusted) = 0.542). The smaller cerebral white matter volume mediated the association between childhood poverty and poorer school performance in Dutch children. Our findings point to the importance of poverty exposure in the fetal period and suggest different mechanisms and vulnerabilities across majority/minority groups. |
format | Online Article Text |
id | pubmed-9870876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98708762023-01-25 Poverty from fetal life onward and child brain morphology Koyama, Yuna Hidalgo, Andrea P. Cortes Lacey, Rebecca E. White, Tonya Jansen, Pauline W. Fujiwara, Takeo Tiemeier, Henning Sci Rep Article Poverty is a risk factor for impaired child development, an association possibly mediated by brain morphology. Previous studies lacked prospective poverty assessments during pregnancy and did not stratify by majority/minority status. We investigated the association of household poverty from fetal life forward with brain morphological differences at age 10 years, in 2166 mother–child dyads. Overall, the results showed no associations between any poverty exposure early in life and brain volumes. However, there was the evidence of timing effects: children exposed to poverty in utero had smaller amygdala volumes (B = − 0.18, 95%CI − 0.30; − 0.07, p(FDR-adjusted) = 0.009). There were also differences in associations by majority/minority status (cerebral white matter: p for interaction = 0.04). Dutch children exposed to childhood poverty showed smaller cerebral white matter volumes than their control (B = − 0.26, 95%CI − 0.45; − 0.06, p(FDR-adjusted) = 0.035). This association was not observed in the minority population (B = − 0.05, 95%CI − 0.23; 0.12, p(FDR-adjusted) = 0.542). The smaller cerebral white matter volume mediated the association between childhood poverty and poorer school performance in Dutch children. Our findings point to the importance of poverty exposure in the fetal period and suggest different mechanisms and vulnerabilities across majority/minority groups. Nature Publishing Group UK 2023-01-23 /pmc/articles/PMC9870876/ /pubmed/36690659 http://dx.doi.org/10.1038/s41598-023-28120-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Koyama, Yuna Hidalgo, Andrea P. Cortes Lacey, Rebecca E. White, Tonya Jansen, Pauline W. Fujiwara, Takeo Tiemeier, Henning Poverty from fetal life onward and child brain morphology |
title | Poverty from fetal life onward and child brain morphology |
title_full | Poverty from fetal life onward and child brain morphology |
title_fullStr | Poverty from fetal life onward and child brain morphology |
title_full_unstemmed | Poverty from fetal life onward and child brain morphology |
title_short | Poverty from fetal life onward and child brain morphology |
title_sort | poverty from fetal life onward and child brain morphology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9870876/ https://www.ncbi.nlm.nih.gov/pubmed/36690659 http://dx.doi.org/10.1038/s41598-023-28120-2 |
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