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Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood

BACKGROUND: The etiology and mechanism of spontaneous preterm birth (sPTB) are still unclear. Accumulating evidence has documented that various environmental exposure scenarios may cause maternal and fetal epigenetic changes, which initiates the focus on whether epigenetics can contribute to the occ...

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Autores principales: Wang, Xi-Meng, Tian, Fu-Ying, Fan, Li-Jun, Xie, Chuan-Bo, Niu, Zhong-Zheng, Chen, Wei-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318854/
https://www.ncbi.nlm.nih.gov/pubmed/30606219
http://dx.doi.org/10.1186/s12920-018-0466-3
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author Wang, Xi-Meng
Tian, Fu-Ying
Fan, Li-Jun
Xie, Chuan-Bo
Niu, Zhong-Zheng
Chen, Wei-Qing
author_facet Wang, Xi-Meng
Tian, Fu-Ying
Fan, Li-Jun
Xie, Chuan-Bo
Niu, Zhong-Zheng
Chen, Wei-Qing
author_sort Wang, Xi-Meng
collection PubMed
description BACKGROUND: The etiology and mechanism of spontaneous preterm birth (sPTB) are still unclear. Accumulating evidence has documented that various environmental exposure scenarios may cause maternal and fetal epigenetic changes, which initiates the focus on whether epigenetics can contribute to the occurrence of sPTB. Therefore, we conducted the current study to examine and compare the DNA methylation changes associated with sPTB in placenta and cord blood. METHODS: This hospital-based case-control study was carried out at three Women and Children’s hospitals in South China, where 32 spontaneous preterm births and 16 term births were recruited. Genome-wide DNA methylation profiles of the placenta and cord blood from these subjects were measured using the Illumina HumanMethylation EPIC BeadChip, and sPTB-associated differential methylated CpG sites were identified using limma regression model, after controlling for major maternal and infant confounders. Further Gene Ontology analysis was performed with PANTHER in order to assess different functional enrichment of the sPTB-associated genes in placenta and cord blood. RESULTS: After controlling for potential confounding factors, one differentially methylated position (DMP) in placenta and 31 DMPs in cord blood were found significantly associated with sPTB (Bonferroni corrected p < 0.05). The sPTB-associated CpG sites in placenta were mapped to genes that showed higher enrichment on biological processes including biological regulation, multicellular organismal process, and especially response to stimulus, while those in cord blood were mapped to genes that had higher enrichment on biological processes concerning cellular process, localization, and particularly metabolic process. CONCLUSION: Findings of this study indicated that DNA methylation alteration in both placenta and cord blood are associated with sPTB, yet the DNA methylation modification patterns may appear differently in placenta and cord blood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12920-018-0466-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-63188542019-01-08 Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood Wang, Xi-Meng Tian, Fu-Ying Fan, Li-Jun Xie, Chuan-Bo Niu, Zhong-Zheng Chen, Wei-Qing BMC Med Genomics Research Article BACKGROUND: The etiology and mechanism of spontaneous preterm birth (sPTB) are still unclear. Accumulating evidence has documented that various environmental exposure scenarios may cause maternal and fetal epigenetic changes, which initiates the focus on whether epigenetics can contribute to the occurrence of sPTB. Therefore, we conducted the current study to examine and compare the DNA methylation changes associated with sPTB in placenta and cord blood. METHODS: This hospital-based case-control study was carried out at three Women and Children’s hospitals in South China, where 32 spontaneous preterm births and 16 term births were recruited. Genome-wide DNA methylation profiles of the placenta and cord blood from these subjects were measured using the Illumina HumanMethylation EPIC BeadChip, and sPTB-associated differential methylated CpG sites were identified using limma regression model, after controlling for major maternal and infant confounders. Further Gene Ontology analysis was performed with PANTHER in order to assess different functional enrichment of the sPTB-associated genes in placenta and cord blood. RESULTS: After controlling for potential confounding factors, one differentially methylated position (DMP) in placenta and 31 DMPs in cord blood were found significantly associated with sPTB (Bonferroni corrected p < 0.05). The sPTB-associated CpG sites in placenta were mapped to genes that showed higher enrichment on biological processes including biological regulation, multicellular organismal process, and especially response to stimulus, while those in cord blood were mapped to genes that had higher enrichment on biological processes concerning cellular process, localization, and particularly metabolic process. CONCLUSION: Findings of this study indicated that DNA methylation alteration in both placenta and cord blood are associated with sPTB, yet the DNA methylation modification patterns may appear differently in placenta and cord blood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12920-018-0466-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-03 /pmc/articles/PMC6318854/ /pubmed/30606219 http://dx.doi.org/10.1186/s12920-018-0466-3 Text en © The Author(s). 2018 Open Access This 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 Research Article
Wang, Xi-Meng
Tian, Fu-Ying
Fan, Li-Jun
Xie, Chuan-Bo
Niu, Zhong-Zheng
Chen, Wei-Qing
Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title_full Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title_fullStr Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title_full_unstemmed Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title_short Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood
title_sort comparison of dna methylation profiles associated with spontaneous preterm birth in placenta and cord blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318854/
https://www.ncbi.nlm.nih.gov/pubmed/30606219
http://dx.doi.org/10.1186/s12920-018-0466-3
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