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Childhood adverse events and BDNF promoter methylation in later-life

Studies have shown that the effects of early-life stress and trauma can be enduring, with long-term negative effects on health. Epigenetics, including DNA methylation, have been implicated as a potential mechanism for these effects. Brain-derived neurotropic factor (BDNF) is a neurotransmitter invol...

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Autores principales: Zhou, Aoshuang, Ancelin, Marie-Laure, Ritchie, Karen, Ryan, Joanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998928/
https://www.ncbi.nlm.nih.gov/pubmed/36911114
http://dx.doi.org/10.3389/fpsyt.2023.1108485
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author Zhou, Aoshuang
Ancelin, Marie-Laure
Ritchie, Karen
Ryan, Joanne
author_facet Zhou, Aoshuang
Ancelin, Marie-Laure
Ritchie, Karen
Ryan, Joanne
author_sort Zhou, Aoshuang
collection PubMed
description Studies have shown that the effects of early-life stress and trauma can be enduring, with long-term negative effects on health. Epigenetics, including DNA methylation, have been implicated as a potential mechanism for these effects. Brain-derived neurotropic factor (BDNF) is a neurotransmitter involved in learning and memory, and altered BDNF promoter methylation measured in peripheral tissue has been found with early-life stress. However, whether such methylation differences remain stable into later life, is unknown. This study aimed to investigate the association between childhood adversity and BDNF promoter methylation in adults aged 65 years and over. Data came from a large study of older community-dwelling individuals in France (ESPRIT). Information on three major childhood adverse events, namely abuse/maltreatment, war/natural disaster, and financial difficulties/poverty, was obtained by retrospective reporting from participants of ESPRIT study. BDNF promoter I and IV methylation was assessed in blood and buccal tissue. Linear regression analysis was performed, adjusting for age, sex, education, depression, and morbidity. Among 927 participants, there was no strong evidence that childhood abuse/maltreatment or financial difficulties/poverty were associated with BDNF methylation in older individuals. For war/natural disaster, differential methylation at four of twenty-nine CpG sites was observed, however, these would not have remained significant after correction for multiple testing. Together, these findings do not support a long-term association between adverse childhood events and BDNF methylation in older age, but further large prospective studies are needed, which do not target specific genes, but consider DNA methylation across the genome.
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spelling pubmed-99989282023-03-11 Childhood adverse events and BDNF promoter methylation in later-life Zhou, Aoshuang Ancelin, Marie-Laure Ritchie, Karen Ryan, Joanne Front Psychiatry Psychiatry Studies have shown that the effects of early-life stress and trauma can be enduring, with long-term negative effects on health. Epigenetics, including DNA methylation, have been implicated as a potential mechanism for these effects. Brain-derived neurotropic factor (BDNF) is a neurotransmitter involved in learning and memory, and altered BDNF promoter methylation measured in peripheral tissue has been found with early-life stress. However, whether such methylation differences remain stable into later life, is unknown. This study aimed to investigate the association between childhood adversity and BDNF promoter methylation in adults aged 65 years and over. Data came from a large study of older community-dwelling individuals in France (ESPRIT). Information on three major childhood adverse events, namely abuse/maltreatment, war/natural disaster, and financial difficulties/poverty, was obtained by retrospective reporting from participants of ESPRIT study. BDNF promoter I and IV methylation was assessed in blood and buccal tissue. Linear regression analysis was performed, adjusting for age, sex, education, depression, and morbidity. Among 927 participants, there was no strong evidence that childhood abuse/maltreatment or financial difficulties/poverty were associated with BDNF methylation in older individuals. For war/natural disaster, differential methylation at four of twenty-nine CpG sites was observed, however, these would not have remained significant after correction for multiple testing. Together, these findings do not support a long-term association between adverse childhood events and BDNF methylation in older age, but further large prospective studies are needed, which do not target specific genes, but consider DNA methylation across the genome. Frontiers Media S.A. 2023-02-24 /pmc/articles/PMC9998928/ /pubmed/36911114 http://dx.doi.org/10.3389/fpsyt.2023.1108485 Text en Copyright © 2023 Zhou, Ancelin, Ritchie and Ryan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Zhou, Aoshuang
Ancelin, Marie-Laure
Ritchie, Karen
Ryan, Joanne
Childhood adverse events and BDNF promoter methylation in later-life
title Childhood adverse events and BDNF promoter methylation in later-life
title_full Childhood adverse events and BDNF promoter methylation in later-life
title_fullStr Childhood adverse events and BDNF promoter methylation in later-life
title_full_unstemmed Childhood adverse events and BDNF promoter methylation in later-life
title_short Childhood adverse events and BDNF promoter methylation in later-life
title_sort childhood adverse events and bdnf promoter methylation in later-life
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998928/
https://www.ncbi.nlm.nih.gov/pubmed/36911114
http://dx.doi.org/10.3389/fpsyt.2023.1108485
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