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Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study
BACKGROUND: Eating disorders (ED) are chronic psychiatric disorders, common amongst women of reproductive age. ED in pregnancy are associated with poor nutrition and abnormal intrauterine growth. Increasing evidence also shows offspring of women with ED have adverse developmental and birth outcomes....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659017/ https://www.ncbi.nlm.nih.gov/pubmed/29093763 http://dx.doi.org/10.1186/s13148-017-0418-3 |
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author | Kazmi, Nabila Gaunt, Tom R. Relton, Caroline Micali, Nadia |
author_facet | Kazmi, Nabila Gaunt, Tom R. Relton, Caroline Micali, Nadia |
author_sort | Kazmi, Nabila |
collection | PubMed |
description | BACKGROUND: Eating disorders (ED) are chronic psychiatric disorders, common amongst women of reproductive age. ED in pregnancy are associated with poor nutrition and abnormal intrauterine growth. Increasing evidence also shows offspring of women with ED have adverse developmental and birth outcomes. We sought to carry out the first study investigating DNA methylation in offspring of women with ED. We compared cord blood DNA methylation in offspring of women with active ED (n = 21), past ED (n = 43) and age- and social class-matched controls (n = 126) as part of the Avon Longitudinal Study of Parents and Children. RESULTS: Offspring of women with both active and past ED had lower whole-genome methylation compared to controls (active ED 49.1% (95% confidence intervals 50.5–47.7%), past ED 49.2% (95% CI 50.7–47.7.0%), controls 52.4% (95% CI 53.0%–51.0%)). Amongst offspring of ED women, those born to women with restrictive-type and purging-type ED had lower methylation levels compared to those of controls. Offspring of women with an active restrictive ED in pregnancy had lower whole-genome methylation compared to offspring of women with past restrictive ED. We observed decreased methylation at the DHCR24 locus in offspring of women with active pregnancy ED (effect size (ES) = − 0.124, p = 6.94 × 10(−8)) and increased methylation at the LGALS2 locus in offspring of women with past ED (ES = 0.07, p = 3.74 × 10(−7)) compared to controls. CONCLUSIONS: Maternal active and past ED are associated with differences in offspring whole-genome methylation. Our results show altered DNA methylation in loci relevant to metabolism; these might be biomarkers of disrupted metabolic pathways in offspring of ED mothers. Further work is needed to examine potential mechanisms and functional outcomes of the observed methylation patterns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-017-0418-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5659017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56590172017-11-01 Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study Kazmi, Nabila Gaunt, Tom R. Relton, Caroline Micali, Nadia Clin Epigenetics Research BACKGROUND: Eating disorders (ED) are chronic psychiatric disorders, common amongst women of reproductive age. ED in pregnancy are associated with poor nutrition and abnormal intrauterine growth. Increasing evidence also shows offspring of women with ED have adverse developmental and birth outcomes. We sought to carry out the first study investigating DNA methylation in offspring of women with ED. We compared cord blood DNA methylation in offspring of women with active ED (n = 21), past ED (n = 43) and age- and social class-matched controls (n = 126) as part of the Avon Longitudinal Study of Parents and Children. RESULTS: Offspring of women with both active and past ED had lower whole-genome methylation compared to controls (active ED 49.1% (95% confidence intervals 50.5–47.7%), past ED 49.2% (95% CI 50.7–47.7.0%), controls 52.4% (95% CI 53.0%–51.0%)). Amongst offspring of ED women, those born to women with restrictive-type and purging-type ED had lower methylation levels compared to those of controls. Offspring of women with an active restrictive ED in pregnancy had lower whole-genome methylation compared to offspring of women with past restrictive ED. We observed decreased methylation at the DHCR24 locus in offspring of women with active pregnancy ED (effect size (ES) = − 0.124, p = 6.94 × 10(−8)) and increased methylation at the LGALS2 locus in offspring of women with past ED (ES = 0.07, p = 3.74 × 10(−7)) compared to controls. CONCLUSIONS: Maternal active and past ED are associated with differences in offspring whole-genome methylation. Our results show altered DNA methylation in loci relevant to metabolism; these might be biomarkers of disrupted metabolic pathways in offspring of ED mothers. Further work is needed to examine potential mechanisms and functional outcomes of the observed methylation patterns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-017-0418-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-27 /pmc/articles/PMC5659017/ /pubmed/29093763 http://dx.doi.org/10.1186/s13148-017-0418-3 Text en © The Author(s). 2017 Open AccessThis 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 Kazmi, Nabila Gaunt, Tom R. Relton, Caroline Micali, Nadia Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title | Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title_full | Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title_fullStr | Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title_full_unstemmed | Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title_short | Maternal eating disorders affect offspring cord blood DNA methylation: a prospective study |
title_sort | maternal eating disorders affect offspring cord blood dna methylation: a prospective study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659017/ https://www.ncbi.nlm.nih.gov/pubmed/29093763 http://dx.doi.org/10.1186/s13148-017-0418-3 |
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