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DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring
Background: We examined whether the effect of maternal smoking during pregnancy on birthweight of the offspring was mediated by smoking-induced changes to DNA methylation in cord blood. Methods: First, we used cord blood of 129 Dutch children exposed to maternal smoking vs 126 unexposed to maternal...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588868/ https://www.ncbi.nlm.nih.gov/pubmed/25862628 http://dx.doi.org/10.1093/ije/dyv048 |
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author | Küpers, Leanne K Xu, Xiaojing Jankipersadsing, Soesma A Vaez, Ahmad la Bastide-van Gemert, Sacha Scholtens, Salome Nolte, Ilja M Richmond, Rebecca C Relton, Caroline L Felix, Janine F Duijts, Liesbeth van Meurs, Joyce B Tiemeier, Henning Jaddoe, Vincent W Wang, Xiaoling Corpeleijn, Eva Snieder, Harold |
author_facet | Küpers, Leanne K Xu, Xiaojing Jankipersadsing, Soesma A Vaez, Ahmad la Bastide-van Gemert, Sacha Scholtens, Salome Nolte, Ilja M Richmond, Rebecca C Relton, Caroline L Felix, Janine F Duijts, Liesbeth van Meurs, Joyce B Tiemeier, Henning Jaddoe, Vincent W Wang, Xiaoling Corpeleijn, Eva Snieder, Harold |
author_sort | Küpers, Leanne K |
collection | PubMed |
description | Background: We examined whether the effect of maternal smoking during pregnancy on birthweight of the offspring was mediated by smoking-induced changes to DNA methylation in cord blood. Methods: First, we used cord blood of 129 Dutch children exposed to maternal smoking vs 126 unexposed to maternal and paternal smoking (53% male) participating in the GECKO Drenthe birth cohort. DNA methylation was measured using the Illumina HumanMethylation450 Beadchip. We performed an epigenome-wide association study for the association between maternal smoking and methylation followed by a mediation analysis of the top signals [false-discovery rate (FDR) < 0.05]. We adjusted both analyses for maternal age, education, pre-pregnancy BMI, offspring’s sex, gestational age and white blood cell composition. Secondly, in 175 exposed and 1248 unexposed newborns from two independent birth cohorts, we replicated and meta-analysed results of eight cytosine-phosphate-guanine (CpG) sites in the GFI1 gene, which showed the most robust mediation. Finally, we performed functional network and enrichment analysis. Results: We found 35 differentially methylated CpGs (FDR < 0.05) in newborns exposed vs unexposed to smoking, of which 23 survived Bonferroni correction (P < 1 × 10(-7)). These 23 CpGs mapped to eight genes: AHRR, GFI1, MYO1G, CYP1A1, NEUROG1, CNTNAP2, FRMD4A and LRP5. We observed partial confirmation as three of the eight CpGs in GFI1 replicated. These CpGs partly mediated the effect of maternal smoking on birthweight (Sobel P < 0.05) in meta-analysis of GECKO and the two replication cohorts. Differential methylation of these three GFI1 CpGs explained 12–19% of the 202 g lower birthweight in smoking mothers. Functional enrichment analysis pointed towards activation of cell-mediated immunity. Conclusions: Maternal smoking during pregnancy was associated with cord blood methylation differences. We observed a potentially mediating role of methylation in the association between maternal smoking during pregnancy and birthweight of the offspring. Functional network analysis suggested a role in activating the immune system. |
format | Online Article Text |
id | pubmed-4588868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45888682015-10-01 DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring Küpers, Leanne K Xu, Xiaojing Jankipersadsing, Soesma A Vaez, Ahmad la Bastide-van Gemert, Sacha Scholtens, Salome Nolte, Ilja M Richmond, Rebecca C Relton, Caroline L Felix, Janine F Duijts, Liesbeth van Meurs, Joyce B Tiemeier, Henning Jaddoe, Vincent W Wang, Xiaoling Corpeleijn, Eva Snieder, Harold Int J Epidemiol Early Life Environment Background: We examined whether the effect of maternal smoking during pregnancy on birthweight of the offspring was mediated by smoking-induced changes to DNA methylation in cord blood. Methods: First, we used cord blood of 129 Dutch children exposed to maternal smoking vs 126 unexposed to maternal and paternal smoking (53% male) participating in the GECKO Drenthe birth cohort. DNA methylation was measured using the Illumina HumanMethylation450 Beadchip. We performed an epigenome-wide association study for the association between maternal smoking and methylation followed by a mediation analysis of the top signals [false-discovery rate (FDR) < 0.05]. We adjusted both analyses for maternal age, education, pre-pregnancy BMI, offspring’s sex, gestational age and white blood cell composition. Secondly, in 175 exposed and 1248 unexposed newborns from two independent birth cohorts, we replicated and meta-analysed results of eight cytosine-phosphate-guanine (CpG) sites in the GFI1 gene, which showed the most robust mediation. Finally, we performed functional network and enrichment analysis. Results: We found 35 differentially methylated CpGs (FDR < 0.05) in newborns exposed vs unexposed to smoking, of which 23 survived Bonferroni correction (P < 1 × 10(-7)). These 23 CpGs mapped to eight genes: AHRR, GFI1, MYO1G, CYP1A1, NEUROG1, CNTNAP2, FRMD4A and LRP5. We observed partial confirmation as three of the eight CpGs in GFI1 replicated. These CpGs partly mediated the effect of maternal smoking on birthweight (Sobel P < 0.05) in meta-analysis of GECKO and the two replication cohorts. Differential methylation of these three GFI1 CpGs explained 12–19% of the 202 g lower birthweight in smoking mothers. Functional enrichment analysis pointed towards activation of cell-mediated immunity. Conclusions: Maternal smoking during pregnancy was associated with cord blood methylation differences. We observed a potentially mediating role of methylation in the association between maternal smoking during pregnancy and birthweight of the offspring. Functional network analysis suggested a role in activating the immune system. Oxford University Press 2015-08 2015-04-10 /pmc/articles/PMC4588868/ /pubmed/25862628 http://dx.doi.org/10.1093/ije/dyv048 Text en © The Author 2015. Published by Oxford University Press on behalf of the International Epidemiological Association http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Early Life Environment Küpers, Leanne K Xu, Xiaojing Jankipersadsing, Soesma A Vaez, Ahmad la Bastide-van Gemert, Sacha Scholtens, Salome Nolte, Ilja M Richmond, Rebecca C Relton, Caroline L Felix, Janine F Duijts, Liesbeth van Meurs, Joyce B Tiemeier, Henning Jaddoe, Vincent W Wang, Xiaoling Corpeleijn, Eva Snieder, Harold DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title | DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title_full | DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title_fullStr | DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title_full_unstemmed | DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title_short | DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
title_sort | dna methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring |
topic | Early Life Environment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588868/ https://www.ncbi.nlm.nih.gov/pubmed/25862628 http://dx.doi.org/10.1093/ije/dyv048 |
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