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Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children

OBJECTIVE: The objective of this study was to evaluate the relationship between ACEs and inflammatory profiles (i.e., pro- and anti-) in early childhood and to examine whether patterns differ for racial/ethnic subgroups. STUDY DESIGN: Using longitudinal data from the Multidimensional Assessment of P...

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Autores principales: Heard-Garris, Nia, Davis, Matthew M., Estabrook, Ryne, Burns, James, Briggs-Gowan, Margaret, Allen, Norrina, Carnethon, Mercedes, Aguayo, Liliana, Wakschlag, Lauren, Penedo, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474684/
http://dx.doi.org/10.1016/j.bbih.2019.100006
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author Heard-Garris, Nia
Davis, Matthew M.
Estabrook, Ryne
Burns, James
Briggs-Gowan, Margaret
Allen, Norrina
Carnethon, Mercedes
Aguayo, Liliana
Wakschlag, Lauren
Penedo, Frank
author_facet Heard-Garris, Nia
Davis, Matthew M.
Estabrook, Ryne
Burns, James
Briggs-Gowan, Margaret
Allen, Norrina
Carnethon, Mercedes
Aguayo, Liliana
Wakschlag, Lauren
Penedo, Frank
author_sort Heard-Garris, Nia
collection PubMed
description OBJECTIVE: The objective of this study was to evaluate the relationship between ACEs and inflammatory profiles (i.e., pro- and anti-) in early childhood and to examine whether patterns differ for racial/ethnic subgroups. STUDY DESIGN: Using longitudinal data from the Multidimensional Assessment of Preschoolers Study (MAPS) (N = 122), we examined the relationship between adverse childhood experiences (ACEs) beginning at birth, C -reactive protein (CRP), and both pro-inflammatory (i.e., IL-1 β, IL-6, TNF, and CRP) and anti-inflammatory (i.e. IL-4 and IL-10) biomarkers during early school age (ages 6–8 years). RESULTS: No children in the sample were reported to have experienced 0 ACES, 7% had 1 ACE, 51% had 2-3 ACEs, and 42% had 4 or more ACEs accumulated by the early school-age wave (ESA). There were no significant associations between cumulative ACEs and inflammatory markers. However, parental substance abuse, a specific ACE, was positively correlated with a pro-inflammatory profile at early school age (r = 0.18, p<.05). Specifically, substance abuse as an ACE was associated with higher levels of pro-inflammatory markers such as IL-1 β and IL-6. Additionally, Hispanics with ACEs had higher levels of CRP than Black and white individuals. CONCLUSIONS: Children with histories of ACEs, especially those with parental substance abuse, may have higher levels of inflammation. Better understanding the role of inflammation in the development of chronic diseases for individuals with ACEs may allow earlier identification and prevention of disease during childhood for those at the highest risk.
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spelling pubmed-84746842021-09-28 Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children Heard-Garris, Nia Davis, Matthew M. Estabrook, Ryne Burns, James Briggs-Gowan, Margaret Allen, Norrina Carnethon, Mercedes Aguayo, Liliana Wakschlag, Lauren Penedo, Frank Brain Behav Immun Health Full Length Article OBJECTIVE: The objective of this study was to evaluate the relationship between ACEs and inflammatory profiles (i.e., pro- and anti-) in early childhood and to examine whether patterns differ for racial/ethnic subgroups. STUDY DESIGN: Using longitudinal data from the Multidimensional Assessment of Preschoolers Study (MAPS) (N = 122), we examined the relationship between adverse childhood experiences (ACEs) beginning at birth, C -reactive protein (CRP), and both pro-inflammatory (i.e., IL-1 β, IL-6, TNF, and CRP) and anti-inflammatory (i.e. IL-4 and IL-10) biomarkers during early school age (ages 6–8 years). RESULTS: No children in the sample were reported to have experienced 0 ACES, 7% had 1 ACE, 51% had 2-3 ACEs, and 42% had 4 or more ACEs accumulated by the early school-age wave (ESA). There were no significant associations between cumulative ACEs and inflammatory markers. However, parental substance abuse, a specific ACE, was positively correlated with a pro-inflammatory profile at early school age (r = 0.18, p<.05). Specifically, substance abuse as an ACE was associated with higher levels of pro-inflammatory markers such as IL-1 β and IL-6. Additionally, Hispanics with ACEs had higher levels of CRP than Black and white individuals. CONCLUSIONS: Children with histories of ACEs, especially those with parental substance abuse, may have higher levels of inflammation. Better understanding the role of inflammation in the development of chronic diseases for individuals with ACEs may allow earlier identification and prevention of disease during childhood for those at the highest risk. Elsevier 2019-11-14 /pmc/articles/PMC8474684/ http://dx.doi.org/10.1016/j.bbih.2019.100006 Text en © 2019 Published by Elsevier Inc. https://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 Full Length Article
Heard-Garris, Nia
Davis, Matthew M.
Estabrook, Ryne
Burns, James
Briggs-Gowan, Margaret
Allen, Norrina
Carnethon, Mercedes
Aguayo, Liliana
Wakschlag, Lauren
Penedo, Frank
Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title_full Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title_fullStr Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title_full_unstemmed Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title_short Adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
title_sort adverse childhood experiences and biomarkers of inflammation in a diverse cohort of early school-aged children
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474684/
http://dx.doi.org/10.1016/j.bbih.2019.100006
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