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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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.
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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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