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Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood

BACKGROUND: Maternal stress during pregnancy is one of the major adverse environmental factors in utero that is capable of influencing health outcomes of the offspring throughout life. Both genetic and epigenetic processes are susceptible to environmental insults in utero and are potential biomarker...

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Autores principales: Chen, Jia, Li, Qian, Rialdi, Alexender, Mystal, Elana, Ly, Jenny, Finik, Jackie, Davey, Taira, Lambertini, Luca, Nomura, Yoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020835/
https://www.ncbi.nlm.nih.gov/pubmed/29963333
http://dx.doi.org/10.4172/2167-1044.1000152
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author Chen, Jia
Li, Qian
Rialdi, Alexender
Mystal, Elana
Ly, Jenny
Finik, Jackie
Davey, Taira
Lambertini, Luca
Nomura, Yoko
author_facet Chen, Jia
Li, Qian
Rialdi, Alexender
Mystal, Elana
Ly, Jenny
Finik, Jackie
Davey, Taira
Lambertini, Luca
Nomura, Yoko
author_sort Chen, Jia
collection PubMed
description BACKGROUND: Maternal stress during pregnancy is one of the major adverse environmental factors in utero that is capable of influencing health outcomes of the offspring throughout life. Both genetic and epigenetic processes are susceptible to environmental insults in utero and are potential biomarkers of the experienced environment including maternal stress. METHODS: We profiled expression level of six genes in hypothalamic pituitary adrenal (HPA) axis functioning (HSD11B2, SLC6A4, NR3C1, NR3C2, CRHR1 and CRHR2), two imprinted genes (IGF2 and H19) and one neurodevelopmental gene (EGR1), from 49 pairs of placenta and umbilical cord blood (UCB) samples from a birth cohort. We also assessed global methylation levels by LUminometric Methylation Assay (LUMA) and methylation at the imprinting control region (ICR) of IGF2/H19. RESULTS: Little correlations between paired placenta and UCB were observed except H19 expression (r = 0.31, P = 0.04) and IGF2/H19 ICR methylation (r = 0.43, P = 0.01); gene expression levels were significantly higher (P < 0.001) in placenta than UCB except CRHR1 and CRHR2, which were unexpressed in placenta. Maternal stress correlated higher levels of HPA genes and lower levels of EGR1 and LUMA, but only in placenta. Positive association between maternal stress and IGF2/H19 ICR methylation was present in both placenta and UCB. CONCLUSIONS: Our findings support the notion that adverse in utero environment, as measured by antenatal maternal stress, depression and anxiety, can be observed in the epi/genome of the relevant tissues, i.e. placenta and UCBs, leading to development of molecular markers for assessing in utero adversities.
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spelling pubmed-60208352018-06-27 Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood Chen, Jia Li, Qian Rialdi, Alexender Mystal, Elana Ly, Jenny Finik, Jackie Davey, Taira Lambertini, Luca Nomura, Yoko J Depress Anxiety Article BACKGROUND: Maternal stress during pregnancy is one of the major adverse environmental factors in utero that is capable of influencing health outcomes of the offspring throughout life. Both genetic and epigenetic processes are susceptible to environmental insults in utero and are potential biomarkers of the experienced environment including maternal stress. METHODS: We profiled expression level of six genes in hypothalamic pituitary adrenal (HPA) axis functioning (HSD11B2, SLC6A4, NR3C1, NR3C2, CRHR1 and CRHR2), two imprinted genes (IGF2 and H19) and one neurodevelopmental gene (EGR1), from 49 pairs of placenta and umbilical cord blood (UCB) samples from a birth cohort. We also assessed global methylation levels by LUminometric Methylation Assay (LUMA) and methylation at the imprinting control region (ICR) of IGF2/H19. RESULTS: Little correlations between paired placenta and UCB were observed except H19 expression (r = 0.31, P = 0.04) and IGF2/H19 ICR methylation (r = 0.43, P = 0.01); gene expression levels were significantly higher (P < 0.001) in placenta than UCB except CRHR1 and CRHR2, which were unexpressed in placenta. Maternal stress correlated higher levels of HPA genes and lower levels of EGR1 and LUMA, but only in placenta. Positive association between maternal stress and IGF2/H19 ICR methylation was present in both placenta and UCB. CONCLUSIONS: Our findings support the notion that adverse in utero environment, as measured by antenatal maternal stress, depression and anxiety, can be observed in the epi/genome of the relevant tissues, i.e. placenta and UCBs, leading to development of molecular markers for assessing in utero adversities. 2014-02-25 2014 /pmc/articles/PMC6020835/ /pubmed/29963333 http://dx.doi.org/10.4172/2167-1044.1000152 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Chen, Jia
Li, Qian
Rialdi, Alexender
Mystal, Elana
Ly, Jenny
Finik, Jackie
Davey, Taira
Lambertini, Luca
Nomura, Yoko
Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title_full Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title_fullStr Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title_full_unstemmed Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title_short Influences of Maternal Stress during Pregnancy on the Epi/genome: Comparison of Placenta and Umbilical Cord Blood
title_sort influences of maternal stress during pregnancy on the epi/genome: comparison of placenta and umbilical cord blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020835/
https://www.ncbi.nlm.nih.gov/pubmed/29963333
http://dx.doi.org/10.4172/2167-1044.1000152
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