BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma

The gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent stu...

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Published inClinical epigenetics Vol. 9; no. 1; pp. 68 - 12
Main Authors Kertes, Darlene A, Bhatt, Samarth S, Kamin, Hayley S, Hughes, David A, Rodney, Nicole C, Mulligan, Connie J
Format Journal Article
LanguageEnglish
Published Germany BioMed Central Ltd 30.06.2017
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Abstract The gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and methylation in humans. This study examined associations of prenatal exposure to maternal stress and methylation at CpG sites across the gene. Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. This is the first study in humans to examine methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth.
AbstractList Background The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters BDNF methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and BDNF methylation in humans. This study examined associations of prenatal exposure to maternal stress and BDNF methylation at CpG sites across the BDNF gene. Results Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with BDNF methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and BDNF methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. Conclusions This is the first study in humans to examine BDNF methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and BDNF methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth. Keywords: Brain-derived neurotrophic factor, BDNF, Stress, Trauma, War, Prenatal, DNA methylation, Transcription factor, Blood, Placenta
Abstract Background The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters BDNF methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and BDNF methylation in humans. This study examined associations of prenatal exposure to maternal stress and BDNF methylation at CpG sites across the BDNF gene. Results Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with BDNF methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and BDNF methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. Conclusions This is the first study in humans to examine BDNF methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and BDNF methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth.
The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters BDNF methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and BDNF methylation in humans. This study examined associations of prenatal exposure to maternal stress and BDNF methylation at CpG sites across the BDNF gene. Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with BDNF methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and BDNF methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. This is the first study in humans to examine BDNF methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and BDNF methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth.
The gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and methylation in humans. This study examined associations of prenatal exposure to maternal stress and methylation at CpG sites across the gene. Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. This is the first study in humans to examine methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth.
Background The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in both the brain and periphery, BDNF plays critical roles throughout the body and is essential for placental and fetal development. Rodent studies show that early life stress, including prenatal stress, broadly alters BDNF methylation, with presumed changes in gene expression. No studies have assessed prenatal exposure to maternal traumatic stress and BDNF methylation in humans. This study examined associations of prenatal exposure to maternal stress and BDNF methylation at CpG sites across the BDNF gene. Results Among 24 mothers and newborns in the eastern Democratic Republic of Congo, a region with extreme conflict and violence to women, maternal experiences of war trauma and chronic stress were associated with BDNF methylation in umbilical cord blood, placental tissue, and maternal venous blood. Associations of maternal stress and BDNF methylation showed high tissue specificity. The majority of significant associations were observed in putative transcription factor binding regions. Conclusions This is the first study in humans to examine BDNF methylation in relation to prenatal exposure to maternal stress in three tissues simultaneously and the first in any mammalian species to report associations of prenatal stress and BDNF methylation in placental tissue. The findings add to the growing body of evidence highlighting the importance of considering epigenetic effects when examining the impacts of trauma and stress, not only for adults but also for offspring exposed via effects transmitted before birth.
ArticleNumber 68
Audience Academic
Author Hughes, David A
Rodney, Nicole C
Kamin, Hayley S
Mulligan, Connie J
Kertes, Darlene A
Bhatt, Samarth S
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  fullname: Kertes, Darlene A
  organization: Department of Psychology and University of Florida Genetics Institute, 945 Center Drive, Gainesville, FL 32611-2250 USA
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  givenname: Samarth S
  surname: Bhatt
  fullname: Bhatt, Samarth S
  organization: Department of Psychology, University of Florida, Gainesville, FL USA
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  surname: Kamin
  fullname: Kamin, Hayley S
  organization: Department of Psychology, University of Florida, Gainesville, FL USA
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  givenname: David A
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  fullname: Hughes, David A
  organization: Integrative Epidemiology Unit, University of Bristol, Bristol, UK
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  givenname: Nicole C
  surname: Rodney
  fullname: Rodney, Nicole C
  organization: Department of Anthropology, University of Florida, Gainesville, FL USA
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  givenname: Connie J
  surname: Mulligan
  fullname: Mulligan, Connie J
  organization: Department of Anthropology and University of Florida Genetics Institute, University of Florida, Gainesville, FL USA
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Issue 1
Keywords Prenatal
Brain-derived neurotrophic factor
Placenta
BDNF
DNA methylation
War
Transcription factor
Trauma
Blood
Stress
Language English
License 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.
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SSID ssj0000399910
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Snippet The gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity. Present in...
Background The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic...
The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and synaptic plasticity....
Abstract Background The BDNF gene codes for brain-derived neurotrophic factor, a growth factor involved in neural development, cell differentiation, and...
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StartPage 68
SubjectTerms Aggression
Alcohol
Anxiety
BDNF
Bioinformatics
Brain research
Brain-derived neurotrophic factor
Brain-Derived Neurotrophic Factor - blood
Brain-Derived Neurotrophic Factor - genetics
Congo
Cord blood
CpG islands
Deoxyribonucleic acid
DNA
DNA Methylation
Domestic violence
Epigenetics
Female
Fetal Blood - chemistry
Fetuses
Gene expression
Genetic aspects
Genetic Association Studies
Genomes
Health aspects
Humans
Infant, Newborn
Maternal Exposure
Maternal-fetal exchange
Neonates
Neural plasticity
Organ Specificity
Outdoor air quality
Placenta
Placenta - chemistry
Pregnancy
Prenatal
Prenatal experience
Prenatal exposure
Psychological Trauma
Stress
Studies
Synaptic plasticity
Synaptogenesis
Transcription factors
Trauma
Umbilical cord
War
War Exposure
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Title BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma
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