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Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years
Epigenetic factors have been suggested as mediators of early-life nutrition to future health. Prior studies focused on breastfeeding effects on DNA methylation (DNAm), ignoring other feeding modes. In this analysis of the Isle of Wight birth cohort, feeding modes were categorized as exclusive breast...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824231/ https://www.ncbi.nlm.nih.gov/pubmed/33396735 http://dx.doi.org/10.3390/nu13010099 |
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author | Mallisetty, Yamini Mukherjee, Nandini Jiang, Yu Chen, Su Ewart, Susan Arshad, S. Hasan Holloway, John W. Zhang, Hongmei Karmaus, Wilfried |
author_facet | Mallisetty, Yamini Mukherjee, Nandini Jiang, Yu Chen, Su Ewart, Susan Arshad, S. Hasan Holloway, John W. Zhang, Hongmei Karmaus, Wilfried |
author_sort | Mallisetty, Yamini |
collection | PubMed |
description | Epigenetic factors have been suggested as mediators of early-life nutrition to future health. Prior studies focused on breastfeeding effects on DNA methylation (DNAm), ignoring other feeding modes. In this analysis of the Isle of Wight birth cohort, feeding modes were categorized as exclusive breastfeeding (EBF), exclusive formula feeding (EFF), and mixed feeding based on whether the respective feeding mode lasted for at least 3 months. In addition, in the past, infant feeding modes were assessed using DNAm at one time point in childhood, not changes of DNAm. In this paper, methylation differences (delta DNAm) were calculated by subtracting residual methylation values at birth from age 10 years (adjusting for cell types and season of blood collection at both ages). These deltas were estimated for all methylation sites where cytosine was followed by guanine (cytosine guanine dinucleotide (CpG) sites). Then, we performed an epigenome-wide association study contrasting EBF, EFF, and mixed feeding with delta DNAm that represents changes in methylation from birth to 10 years. A total of 87 CpGs (EBF: 27 CpGs, EFF: 48 CpGs, mixed: 12 CpGs) were identified using separate linear regression models adjusting for confounders and multiple testing. The sum of all changes in methylation from birth to age 10 years was significantly lower in the EFF group. Correspondingly, the number of CpGs with a methylation decline was 4.7% higher reflecting 13,683 CpGs. Lower methylation related to exclusive formula feeding and its adverse potential for the child’s development needs future research to reduce adverse health effects. |
format | Online Article Text |
id | pubmed-7824231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78242312021-01-24 Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years Mallisetty, Yamini Mukherjee, Nandini Jiang, Yu Chen, Su Ewart, Susan Arshad, S. Hasan Holloway, John W. Zhang, Hongmei Karmaus, Wilfried Nutrients Article Epigenetic factors have been suggested as mediators of early-life nutrition to future health. Prior studies focused on breastfeeding effects on DNA methylation (DNAm), ignoring other feeding modes. In this analysis of the Isle of Wight birth cohort, feeding modes were categorized as exclusive breastfeeding (EBF), exclusive formula feeding (EFF), and mixed feeding based on whether the respective feeding mode lasted for at least 3 months. In addition, in the past, infant feeding modes were assessed using DNAm at one time point in childhood, not changes of DNAm. In this paper, methylation differences (delta DNAm) were calculated by subtracting residual methylation values at birth from age 10 years (adjusting for cell types and season of blood collection at both ages). These deltas were estimated for all methylation sites where cytosine was followed by guanine (cytosine guanine dinucleotide (CpG) sites). Then, we performed an epigenome-wide association study contrasting EBF, EFF, and mixed feeding with delta DNAm that represents changes in methylation from birth to 10 years. A total of 87 CpGs (EBF: 27 CpGs, EFF: 48 CpGs, mixed: 12 CpGs) were identified using separate linear regression models adjusting for confounders and multiple testing. The sum of all changes in methylation from birth to age 10 years was significantly lower in the EFF group. Correspondingly, the number of CpGs with a methylation decline was 4.7% higher reflecting 13,683 CpGs. Lower methylation related to exclusive formula feeding and its adverse potential for the child’s development needs future research to reduce adverse health effects. MDPI 2020-12-30 /pmc/articles/PMC7824231/ /pubmed/33396735 http://dx.doi.org/10.3390/nu13010099 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mallisetty, Yamini Mukherjee, Nandini Jiang, Yu Chen, Su Ewart, Susan Arshad, S. Hasan Holloway, John W. Zhang, Hongmei Karmaus, Wilfried Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title | Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title_full | Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title_fullStr | Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title_full_unstemmed | Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title_short | Epigenome-Wide Association of Infant Feeding and Changes in DNA Methylation from Birth to 10 Years |
title_sort | epigenome-wide association of infant feeding and changes in dna methylation from birth to 10 years |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824231/ https://www.ncbi.nlm.nih.gov/pubmed/33396735 http://dx.doi.org/10.3390/nu13010099 |
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