Cargando…

Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns

BACKGROUND: Adverse childhood experiences (ACEs) are correlated with accelerated epigenetic aging, but it is not clear whether altered epigenetic aging from childhood adversities persists into adulthood and can be transmitted to the next generation. Thus, we tested whether mothers’ childhood adversi...

Descripción completa

Detalles Bibliográficos
Autores principales: Dye, Christian K., Wu, Haotian, Monk, Catherine, Belsky, Daniel W., Alschuler, Daniel, Lee, Seonjoo, O’Donnell, Kieran, Scorza, Pamela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028804/
https://www.ncbi.nlm.nih.gov/pubmed/36945654
http://dx.doi.org/10.1101/2023.03.02.530806
_version_ 1784910023527235584
author Dye, Christian K.
Wu, Haotian
Monk, Catherine
Belsky, Daniel W.
Alschuler, Daniel
Lee, Seonjoo
O’Donnell, Kieran
Scorza, Pamela
author_facet Dye, Christian K.
Wu, Haotian
Monk, Catherine
Belsky, Daniel W.
Alschuler, Daniel
Lee, Seonjoo
O’Donnell, Kieran
Scorza, Pamela
author_sort Dye, Christian K.
collection PubMed
description BACKGROUND: Adverse childhood experiences (ACEs) are correlated with accelerated epigenetic aging, but it is not clear whether altered epigenetic aging from childhood adversities persists into adulthood and can be transmitted to the next generation. Thus, we tested whether mothers’ childhood adversity is associated with accelerated epigenetic aging during pregnancy and in their newborn offspring. METHODS: Data were from the Avon Longitudinal Study of Parents and Children (ALSPAC) sub-study, Accessible Resource for Integrated Epigenomic Studies (ARIES). Women provided retrospective self-reports during pregnancy of ACE exposure. DNA methylation was measured in mothers during pregnancy and cord blood at birth. Estimates of epigenetic age acceleration were calculated using Principal Components of Horvath, Hannum skin & blood, GrimAge, PhenoAge, and DunedinPACE epigenetic clocks for mothers; and the Knight and Bohlin cord blood clocks for newborns. Associations between a cumulative maternal ACE score and epigenetic age acceleration were estimated using linear regression models, adjusting for maternal age at pregnancy, smoking during pregnancy, education, and pre-pregnancy BMI. Models for offspring were stratified by sex and additionally adjusted for gestation age. RESULTS: Mothers’ total ACE score was positively associated with accelerated maternal PhenoAge and GrimAge. In newborn offspring, mothers’ total ACE score was positively associated with accelerated epigenetic aging in males using the Bohlin clock, but not in females using either epigenetic clock. We found male offsprings’ epigenetic age was accelerated in those born to mothers exposed to neglect using the Knight clock; and parental substance abuse using the Bohlin clock. CONCLUSION: Our results show that mothers’ ACE exposure is associated with DNAm age acceleration in male offspring, supporting the notion that DNAm age could be a marker of intergenerational biological embedding of mothers’ childhood adversity. This is consistent with findings on vulnerability of male fetuses to environmental insults.
format Online
Article
Text
id pubmed-10028804
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-100288042023-03-22 Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns Dye, Christian K. Wu, Haotian Monk, Catherine Belsky, Daniel W. Alschuler, Daniel Lee, Seonjoo O’Donnell, Kieran Scorza, Pamela bioRxiv Article BACKGROUND: Adverse childhood experiences (ACEs) are correlated with accelerated epigenetic aging, but it is not clear whether altered epigenetic aging from childhood adversities persists into adulthood and can be transmitted to the next generation. Thus, we tested whether mothers’ childhood adversity is associated with accelerated epigenetic aging during pregnancy and in their newborn offspring. METHODS: Data were from the Avon Longitudinal Study of Parents and Children (ALSPAC) sub-study, Accessible Resource for Integrated Epigenomic Studies (ARIES). Women provided retrospective self-reports during pregnancy of ACE exposure. DNA methylation was measured in mothers during pregnancy and cord blood at birth. Estimates of epigenetic age acceleration were calculated using Principal Components of Horvath, Hannum skin & blood, GrimAge, PhenoAge, and DunedinPACE epigenetic clocks for mothers; and the Knight and Bohlin cord blood clocks for newborns. Associations between a cumulative maternal ACE score and epigenetic age acceleration were estimated using linear regression models, adjusting for maternal age at pregnancy, smoking during pregnancy, education, and pre-pregnancy BMI. Models for offspring were stratified by sex and additionally adjusted for gestation age. RESULTS: Mothers’ total ACE score was positively associated with accelerated maternal PhenoAge and GrimAge. In newborn offspring, mothers’ total ACE score was positively associated with accelerated epigenetic aging in males using the Bohlin clock, but not in females using either epigenetic clock. We found male offsprings’ epigenetic age was accelerated in those born to mothers exposed to neglect using the Knight clock; and parental substance abuse using the Bohlin clock. CONCLUSION: Our results show that mothers’ ACE exposure is associated with DNAm age acceleration in male offspring, supporting the notion that DNAm age could be a marker of intergenerational biological embedding of mothers’ childhood adversity. This is consistent with findings on vulnerability of male fetuses to environmental insults. Cold Spring Harbor Laboratory 2023-03-06 /pmc/articles/PMC10028804/ /pubmed/36945654 http://dx.doi.org/10.1101/2023.03.02.530806 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
Dye, Christian K.
Wu, Haotian
Monk, Catherine
Belsky, Daniel W.
Alschuler, Daniel
Lee, Seonjoo
O’Donnell, Kieran
Scorza, Pamela
Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title_full Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title_fullStr Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title_full_unstemmed Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title_short Mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
title_sort mother’s childhood adversity is associated with accelerated epigenetic aging in pregnancy and in male newborns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028804/
https://www.ncbi.nlm.nih.gov/pubmed/36945654
http://dx.doi.org/10.1101/2023.03.02.530806
work_keys_str_mv AT dyechristiank motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT wuhaotian motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT monkcatherine motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT belskydanielw motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT alschulerdaniel motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT leeseonjoo motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT odonnellkieran motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns
AT scorzapamela motherschildhoodadversityisassociatedwithacceleratedepigeneticaginginpregnancyandinmalenewborns