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Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood
BACKGROUND: Poor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are uncle...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010979/ https://www.ncbi.nlm.nih.gov/pubmed/33789736 http://dx.doi.org/10.1186/s13148-021-01056-y |
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author | Pfeiffer, J. R. Bustamante, Angela C. Kim, Grace S. Armstrong, Don Knodt, Annchen R. Koenen, Karestan C. Hariri, Ahmad R. Uddin, Monica |
author_facet | Pfeiffer, J. R. Bustamante, Angela C. Kim, Grace S. Armstrong, Don Knodt, Annchen R. Koenen, Karestan C. Hariri, Ahmad R. Uddin, Monica |
author_sort | Pfeiffer, J. R. |
collection | PubMed |
description | BACKGROUND: Poor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in 5-methyl-cytosine (5mC) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded. RESULTS: In 98 university students aged 18–22 years, retrospective self-reported childhood FEH was associated with right hemisphere hippocampus (b = 10.4, p = 0.005), left hemisphere amygdala (b = 5.3, p = 0.009), and right hemisphere amygdala (b = 5.8, p = 0.016) volumes. After pre-processing and filtering to 5mC probes correlated between saliva and brain, analyses showed that childhood FEH was associated with 49 5mC principal components (module eigengenes; MEs) (p(range) = 3 × 10(–6) to 0.047). Saliva-derived 5mC MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect b = − 111, p = 0.014), and fully mediated the FEH and right amygdala volume relationship (Pink4 ME indirect effect b = − 48, p = 0.026). Modules were enriched with probes falling in genes with immune, central nervous system (CNS), cellular development/differentiation, and metabolic functions. CONCLUSIONS: Findings extend work highlighting neurodevelopmental variability associated with adverse social environment exposure during childhood by specifically implicating poor FEH, while informing a mechanism of biological embedding. FEH-associated epigenetic signatures could function as proxies of altered fronto-limbic grey matter volume associated with poor childhood FEH and inform further investigation into primarily affected tissues such as endocrine, immune, and CNS cell types. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01056-y. |
format | Online Article Text |
id | pubmed-8010979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80109792021-03-31 Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood Pfeiffer, J. R. Bustamante, Angela C. Kim, Grace S. Armstrong, Don Knodt, Annchen R. Koenen, Karestan C. Hariri, Ahmad R. Uddin, Monica Clin Epigenetics Research BACKGROUND: Poor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in 5-methyl-cytosine (5mC) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded. RESULTS: In 98 university students aged 18–22 years, retrospective self-reported childhood FEH was associated with right hemisphere hippocampus (b = 10.4, p = 0.005), left hemisphere amygdala (b = 5.3, p = 0.009), and right hemisphere amygdala (b = 5.8, p = 0.016) volumes. After pre-processing and filtering to 5mC probes correlated between saliva and brain, analyses showed that childhood FEH was associated with 49 5mC principal components (module eigengenes; MEs) (p(range) = 3 × 10(–6) to 0.047). Saliva-derived 5mC MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect b = − 111, p = 0.014), and fully mediated the FEH and right amygdala volume relationship (Pink4 ME indirect effect b = − 48, p = 0.026). Modules were enriched with probes falling in genes with immune, central nervous system (CNS), cellular development/differentiation, and metabolic functions. CONCLUSIONS: Findings extend work highlighting neurodevelopmental variability associated with adverse social environment exposure during childhood by specifically implicating poor FEH, while informing a mechanism of biological embedding. FEH-associated epigenetic signatures could function as proxies of altered fronto-limbic grey matter volume associated with poor childhood FEH and inform further investigation into primarily affected tissues such as endocrine, immune, and CNS cell types. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01056-y. BioMed Central 2021-03-31 /pmc/articles/PMC8010979/ /pubmed/33789736 http://dx.doi.org/10.1186/s13148-021-01056-y Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Pfeiffer, J. R. Bustamante, Angela C. Kim, Grace S. Armstrong, Don Knodt, Annchen R. Koenen, Karestan C. Hariri, Ahmad R. Uddin, Monica Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title | Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title_full | Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title_fullStr | Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title_full_unstemmed | Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title_short | Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood |
title_sort | associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mc in young adulthood |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010979/ https://www.ncbi.nlm.nih.gov/pubmed/33789736 http://dx.doi.org/10.1186/s13148-021-01056-y |
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