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Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review

INTRODUCTION: Epigenetic mechanisms are important for the regulation of gene expression and differentiation in the fetus and the newborn child. Symptoms of maternal depression and antidepressant use affects up to 20 % of pregnant women, and may lead to epigenetic changes with life-long impact on chi...

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Autores principales: Viuff, Anne-Cathrine F., Pedersen, Lars Henning, Kyng, Kasper, Staunstrup, Nicklas Heine, Børglum, Anders, Henriksen, Tine Brink
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015265/
https://www.ncbi.nlm.nih.gov/pubmed/27610205
http://dx.doi.org/10.1186/s13148-016-0262-x
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author Viuff, Anne-Cathrine F.
Pedersen, Lars Henning
Kyng, Kasper
Staunstrup, Nicklas Heine
Børglum, Anders
Henriksen, Tine Brink
author_facet Viuff, Anne-Cathrine F.
Pedersen, Lars Henning
Kyng, Kasper
Staunstrup, Nicklas Heine
Børglum, Anders
Henriksen, Tine Brink
author_sort Viuff, Anne-Cathrine F.
collection PubMed
description INTRODUCTION: Epigenetic mechanisms are important for the regulation of gene expression and differentiation in the fetus and the newborn child. Symptoms of maternal depression and antidepressant use affects up to 20 % of pregnant women, and may lead to epigenetic changes with life-long impact on child health. The aim of this review is to investigate whether there is an association between exposure to maternal antidepressants during pregnancy and epigenetic changes in the newborn. MATERIAL AND METHODS: Systematic literature searches were performed in MEDLINE and EMBASE combining MeSH terms covering epigenetic changes, use of antidepressant medication, pregnancy and newborns. A keyword search was also performed. We included studies on pregnant women and their children where there was a history of maternal depressed mood or anxiety, a reported use of antidepressant medication, and measurements of epigenetic changes in umbilical cord blood. Studies using genome-wide or candidate-based epigenetic analyses were included. Citations and references from the included articles were investigated to locate further relevant articles. The completeness of reporting as well as the risk of bias and confounding was assessed. RESULTS: Six studies were included. They all investigated methylation changes. Genome-wide methylation changes were examined in 184 children and methylation status in specific genes was examined in 96 children exposed to antidepressant medication. Three of the studies found an association between use of antidepressant medication during pregnancy and methylation status at various CpG sites measured in cord blood of the newborn. One of these studies found an association in African-Americans, but not Caucasians. The remaining three studies found associations between maternal mood and epigenetic changes in umbilical cord blood but no association between epigenetic changes and maternal use of antidepressant medication. CONCLUSION: The included studies have not established a clear association between use of antidepressant medication during pregnancy and epigenetic changes in the cord blood. Future studies using newer, more wide-ranging epigenetic methods could discover possible new differentially methylated sites. Larger sample sizes and good validity of exposures are warranted in order to adjust for level of maternal depression, other maternal illness, maternal use of other types of medication, and maternal ethnicity. PROSPERO registration number: CRD42015026575.
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spelling pubmed-50152652016-09-09 Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review Viuff, Anne-Cathrine F. Pedersen, Lars Henning Kyng, Kasper Staunstrup, Nicklas Heine Børglum, Anders Henriksen, Tine Brink Clin Epigenetics Review INTRODUCTION: Epigenetic mechanisms are important for the regulation of gene expression and differentiation in the fetus and the newborn child. Symptoms of maternal depression and antidepressant use affects up to 20 % of pregnant women, and may lead to epigenetic changes with life-long impact on child health. The aim of this review is to investigate whether there is an association between exposure to maternal antidepressants during pregnancy and epigenetic changes in the newborn. MATERIAL AND METHODS: Systematic literature searches were performed in MEDLINE and EMBASE combining MeSH terms covering epigenetic changes, use of antidepressant medication, pregnancy and newborns. A keyword search was also performed. We included studies on pregnant women and their children where there was a history of maternal depressed mood or anxiety, a reported use of antidepressant medication, and measurements of epigenetic changes in umbilical cord blood. Studies using genome-wide or candidate-based epigenetic analyses were included. Citations and references from the included articles were investigated to locate further relevant articles. The completeness of reporting as well as the risk of bias and confounding was assessed. RESULTS: Six studies were included. They all investigated methylation changes. Genome-wide methylation changes were examined in 184 children and methylation status in specific genes was examined in 96 children exposed to antidepressant medication. Three of the studies found an association between use of antidepressant medication during pregnancy and methylation status at various CpG sites measured in cord blood of the newborn. One of these studies found an association in African-Americans, but not Caucasians. The remaining three studies found associations between maternal mood and epigenetic changes in umbilical cord blood but no association between epigenetic changes and maternal use of antidepressant medication. CONCLUSION: The included studies have not established a clear association between use of antidepressant medication during pregnancy and epigenetic changes in the cord blood. Future studies using newer, more wide-ranging epigenetic methods could discover possible new differentially methylated sites. Larger sample sizes and good validity of exposures are warranted in order to adjust for level of maternal depression, other maternal illness, maternal use of other types of medication, and maternal ethnicity. PROSPERO registration number: CRD42015026575. BioMed Central 2016-09-07 /pmc/articles/PMC5015265/ /pubmed/27610205 http://dx.doi.org/10.1186/s13148-016-0262-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Review
Viuff, Anne-Cathrine F.
Pedersen, Lars Henning
Kyng, Kasper
Staunstrup, Nicklas Heine
Børglum, Anders
Henriksen, Tine Brink
Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title_full Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title_fullStr Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title_full_unstemmed Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title_short Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
title_sort antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015265/
https://www.ncbi.nlm.nih.gov/pubmed/27610205
http://dx.doi.org/10.1186/s13148-016-0262-x
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