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The impact of cesarean delivery on infant DNA methylation
BACKGROUND: Mounting evidence suggests that cesarean delivery may have a long-lasting effect on infant health. But the underlying mechanisms remain unclear. This study aims to examine whether cesarean delivery on maternal request without any medical indications (CDMR) impacts DNA methylation status...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011183/ https://www.ncbi.nlm.nih.gov/pubmed/33785011 http://dx.doi.org/10.1186/s12884-021-03748-y |
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author | Chen, Qian Ming, Yanhong Gan, Yuexin Huang, Lisu Zhao, Yanjun Wang, Xia Liu, Yongjie Zhang, Jun |
author_facet | Chen, Qian Ming, Yanhong Gan, Yuexin Huang, Lisu Zhao, Yanjun Wang, Xia Liu, Yongjie Zhang, Jun |
author_sort | Chen, Qian |
collection | PubMed |
description | BACKGROUND: Mounting evidence suggests that cesarean delivery may have a long-lasting effect on infant health. But the underlying mechanisms remain unclear. This study aims to examine whether cesarean delivery on maternal request without any medical indications (CDMR) impacts DNA methylation status in the umbilical cord blood of the infant. METHODS: A cross-sectional study was conducted in Shanghai, China. A total of 70 CDMR and 70 vaginal deliveries (VD) were recruited in 2012. The cord blood DNA methylation status was measured in 30 CDMR and 30 VD newborns using Illumina Infinium Human Methylation 450 K BeadChip. To validate the results, the cord blood DNA methylation status was measured in another 40 CDMR and 40 VD newborns using targeted bisulfite sequencing assay. A total of 497 CpG sites from 40 genes were included in the analysis. RESULTS: A total of 165 differentially methylated positions (DMPs) exhibited differences in DNA methylation by 10% or more between the CDMR and VD groups, many of which were related to the development of the immune system. Based on the targeted bisulfite sequencing assay, 16 genes (16/22, 72.7%) had higher methylation level in the CDMR group than the VD group. Among them, 5 genes were related to the immune system. After considering the estimation of cell type proportions, there was few significant differences in DNA methylation between CDMR and VD groups. CONCLUSIONS: The DMPs identified between CDMR and VD groups might be largely explained by the cell type proportions. Further studies are needed to examine DNA methylation in each cell type separately. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-021-03748-y. |
format | Online Article Text |
id | pubmed-8011183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80111832021-03-31 The impact of cesarean delivery on infant DNA methylation Chen, Qian Ming, Yanhong Gan, Yuexin Huang, Lisu Zhao, Yanjun Wang, Xia Liu, Yongjie Zhang, Jun BMC Pregnancy Childbirth Research Article BACKGROUND: Mounting evidence suggests that cesarean delivery may have a long-lasting effect on infant health. But the underlying mechanisms remain unclear. This study aims to examine whether cesarean delivery on maternal request without any medical indications (CDMR) impacts DNA methylation status in the umbilical cord blood of the infant. METHODS: A cross-sectional study was conducted in Shanghai, China. A total of 70 CDMR and 70 vaginal deliveries (VD) were recruited in 2012. The cord blood DNA methylation status was measured in 30 CDMR and 30 VD newborns using Illumina Infinium Human Methylation 450 K BeadChip. To validate the results, the cord blood DNA methylation status was measured in another 40 CDMR and 40 VD newborns using targeted bisulfite sequencing assay. A total of 497 CpG sites from 40 genes were included in the analysis. RESULTS: A total of 165 differentially methylated positions (DMPs) exhibited differences in DNA methylation by 10% or more between the CDMR and VD groups, many of which were related to the development of the immune system. Based on the targeted bisulfite sequencing assay, 16 genes (16/22, 72.7%) had higher methylation level in the CDMR group than the VD group. Among them, 5 genes were related to the immune system. After considering the estimation of cell type proportions, there was few significant differences in DNA methylation between CDMR and VD groups. CONCLUSIONS: The DMPs identified between CDMR and VD groups might be largely explained by the cell type proportions. Further studies are needed to examine DNA methylation in each cell type separately. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-021-03748-y. BioMed Central 2021-03-30 /pmc/articles/PMC8011183/ /pubmed/33785011 http://dx.doi.org/10.1186/s12884-021-03748-y Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Chen, Qian Ming, Yanhong Gan, Yuexin Huang, Lisu Zhao, Yanjun Wang, Xia Liu, Yongjie Zhang, Jun The impact of cesarean delivery on infant DNA methylation |
title | The impact of cesarean delivery on infant DNA methylation |
title_full | The impact of cesarean delivery on infant DNA methylation |
title_fullStr | The impact of cesarean delivery on infant DNA methylation |
title_full_unstemmed | The impact of cesarean delivery on infant DNA methylation |
title_short | The impact of cesarean delivery on infant DNA methylation |
title_sort | impact of cesarean delivery on infant dna methylation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011183/ https://www.ncbi.nlm.nih.gov/pubmed/33785011 http://dx.doi.org/10.1186/s12884-021-03748-y |
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