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Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness

Recent models propose deoxyribonucleic acid methylation of key neuro-regulatory genes as a molecular mechanism underlying the increased risk of mental disorder associated with early life adversity (ELA). The goal of this study was to examine the association of ELA with oxytocin receptor gene (OXTR)...

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Autores principales: Gouin, J. P., Zhou, Q. Q., Booij, L., Boivin, M., Côté, S. M., Hébert, M., Ouellet-Morin, I., Szyf, M., Tremblay, R. E., Turecki, G., Vitaro, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547144/
https://www.ncbi.nlm.nih.gov/pubmed/28785027
http://dx.doi.org/10.1038/s41598-017-07950-x
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author Gouin, J. P.
Zhou, Q. Q.
Booij, L.
Boivin, M.
Côté, S. M.
Hébert, M.
Ouellet-Morin, I.
Szyf, M.
Tremblay, R. E.
Turecki, G.
Vitaro, F.
author_facet Gouin, J. P.
Zhou, Q. Q.
Booij, L.
Boivin, M.
Côté, S. M.
Hébert, M.
Ouellet-Morin, I.
Szyf, M.
Tremblay, R. E.
Turecki, G.
Vitaro, F.
author_sort Gouin, J. P.
collection PubMed
description Recent models propose deoxyribonucleic acid methylation of key neuro-regulatory genes as a molecular mechanism underlying the increased risk of mental disorder associated with early life adversity (ELA). The goal of this study was to examine the association of ELA with oxytocin receptor gene (OXTR) methylation among young adults. Drawing from a 21-year longitudinal cohort, we compared adulthood OXTR methylation frequency of 46 adults (23 males and 23 females) selected for high or low ELA exposure based on childhood socioeconomic status and exposure to physical and sexual abuse during childhood and adolescence. Associations between OXTR methylation and teacher-rated childhood trajectories of anxiousness were also assessed. ELA exposure was associated with one significant CpG site in the first intron among females, but not among males. Similarly, childhood trajectories of anxiousness were related to one significant CpG site within the promoter region among females, but not among males. This study suggests that females might be more sensitive to the impact of ELA on OXTR methylation than males.
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spelling pubmed-55471442017-08-09 Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness Gouin, J. P. Zhou, Q. Q. Booij, L. Boivin, M. Côté, S. M. Hébert, M. Ouellet-Morin, I. Szyf, M. Tremblay, R. E. Turecki, G. Vitaro, F. Sci Rep Article Recent models propose deoxyribonucleic acid methylation of key neuro-regulatory genes as a molecular mechanism underlying the increased risk of mental disorder associated with early life adversity (ELA). The goal of this study was to examine the association of ELA with oxytocin receptor gene (OXTR) methylation among young adults. Drawing from a 21-year longitudinal cohort, we compared adulthood OXTR methylation frequency of 46 adults (23 males and 23 females) selected for high or low ELA exposure based on childhood socioeconomic status and exposure to physical and sexual abuse during childhood and adolescence. Associations between OXTR methylation and teacher-rated childhood trajectories of anxiousness were also assessed. ELA exposure was associated with one significant CpG site in the first intron among females, but not among males. Similarly, childhood trajectories of anxiousness were related to one significant CpG site within the promoter region among females, but not among males. This study suggests that females might be more sensitive to the impact of ELA on OXTR methylation than males. Nature Publishing Group UK 2017-08-07 /pmc/articles/PMC5547144/ /pubmed/28785027 http://dx.doi.org/10.1038/s41598-017-07950-x Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gouin, J. P.
Zhou, Q. Q.
Booij, L.
Boivin, M.
Côté, S. M.
Hébert, M.
Ouellet-Morin, I.
Szyf, M.
Tremblay, R. E.
Turecki, G.
Vitaro, F.
Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title_full Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title_fullStr Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title_full_unstemmed Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title_short Associations among oxytocin receptor gene (OXTR) DNA methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
title_sort associations among oxytocin receptor gene (oxtr) dna methylation in adulthood, exposure to early life adversity, and childhood trajectories of anxiousness
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547144/
https://www.ncbi.nlm.nih.gov/pubmed/28785027
http://dx.doi.org/10.1038/s41598-017-07950-x
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