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Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains

BACKGROUND: Inadequate maternal nutrition during early fetal development can create permanent alterations in the offspring, leading to poor health outcomes. While nutrients involved in one-carbon cycle metabolism are important to fetal growth, associations with specific nutrients remain inconsistent...

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Autores principales: McCullough, Lauren E., Miller, Erline E., Mendez, Michelle A., Murtha, Amy P., Murphy, Susan K., Hoyo, Cathrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722751/
https://www.ncbi.nlm.nih.gov/pubmed/26807160
http://dx.doi.org/10.1186/s13148-016-0174-9
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author McCullough, Lauren E.
Miller, Erline E.
Mendez, Michelle A.
Murtha, Amy P.
Murphy, Susan K.
Hoyo, Cathrine
author_facet McCullough, Lauren E.
Miller, Erline E.
Mendez, Michelle A.
Murtha, Amy P.
Murphy, Susan K.
Hoyo, Cathrine
author_sort McCullough, Lauren E.
collection PubMed
description BACKGROUND: Inadequate maternal nutrition during early fetal development can create permanent alterations in the offspring, leading to poor health outcomes. While nutrients involved in one-carbon cycle metabolism are important to fetal growth, associations with specific nutrients remain inconsistent. This study estimates associations between maternal vitamins B(12), B(6) (pyridoxal phosphate [PLP] and 4-pyridoxic acid [PA]), and homocysteine (Hcy) concentrations, offspring weight (birth weight and 3-year weight gain), and DNA methylation at four differentially methylated regions (DMRs) known to be involved in fetal growth and development (H19, MEG3, SGCE/PEG10, and PLAGL1). METHODS: Study participants (n = 496) with biomarker and birth weight data were enrolled as part of the Newborn Epigenetics STudy. Weight gain data were available for 273 offspring. Among 484 mother-infant pairs, DNA methylation at regulatory sequences of genomically imprinted genes was measured in umbilical cord blood DNA using bisulfite pyrosequencing. We used generalized linear models to estimate associations. RESULTS: Multivariate adjusted regression models revealed an inverse association between maternal Hcy concentration and male birth weight (β = −210.40, standard error (SE) = 102.08, p = 0.04). The offspring of the mothers in the highest quartile of B(12) experienced lower weight gain between birth and 3 years compared to the offspring of the mothers in the lowest (β = −2203.03, SE = 722.49, p = 0.003). Conversely, maternal PLP was associated with higher weight gain in males; higher maternal PLP concentrations were also associated with offspring DNA methylation levels at the MEG3 DMR (p < 0.01). CONCLUSIONS: While maternal concentrations of B(12), B(6), and Hcy do not associate with birth weight overall, they may play an important role in 3-year weight gain. This is the first study to report an association between maternal PLP and methylation at the MEG3 DMR which may be an important epigenetic tag for maternal B vitamin adequacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0174-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-47227512016-01-23 Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains McCullough, Lauren E. Miller, Erline E. Mendez, Michelle A. Murtha, Amy P. Murphy, Susan K. Hoyo, Cathrine Clin Epigenetics Research BACKGROUND: Inadequate maternal nutrition during early fetal development can create permanent alterations in the offspring, leading to poor health outcomes. While nutrients involved in one-carbon cycle metabolism are important to fetal growth, associations with specific nutrients remain inconsistent. This study estimates associations between maternal vitamins B(12), B(6) (pyridoxal phosphate [PLP] and 4-pyridoxic acid [PA]), and homocysteine (Hcy) concentrations, offspring weight (birth weight and 3-year weight gain), and DNA methylation at four differentially methylated regions (DMRs) known to be involved in fetal growth and development (H19, MEG3, SGCE/PEG10, and PLAGL1). METHODS: Study participants (n = 496) with biomarker and birth weight data were enrolled as part of the Newborn Epigenetics STudy. Weight gain data were available for 273 offspring. Among 484 mother-infant pairs, DNA methylation at regulatory sequences of genomically imprinted genes was measured in umbilical cord blood DNA using bisulfite pyrosequencing. We used generalized linear models to estimate associations. RESULTS: Multivariate adjusted regression models revealed an inverse association between maternal Hcy concentration and male birth weight (β = −210.40, standard error (SE) = 102.08, p = 0.04). The offspring of the mothers in the highest quartile of B(12) experienced lower weight gain between birth and 3 years compared to the offspring of the mothers in the lowest (β = −2203.03, SE = 722.49, p = 0.003). Conversely, maternal PLP was associated with higher weight gain in males; higher maternal PLP concentrations were also associated with offspring DNA methylation levels at the MEG3 DMR (p < 0.01). CONCLUSIONS: While maternal concentrations of B(12), B(6), and Hcy do not associate with birth weight overall, they may play an important role in 3-year weight gain. This is the first study to report an association between maternal PLP and methylation at the MEG3 DMR which may be an important epigenetic tag for maternal B vitamin adequacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0174-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-22 /pmc/articles/PMC4722751/ /pubmed/26807160 http://dx.doi.org/10.1186/s13148-016-0174-9 Text en © McCullough et al. 2016 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
McCullough, Lauren E.
Miller, Erline E.
Mendez, Michelle A.
Murtha, Amy P.
Murphy, Susan K.
Hoyo, Cathrine
Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title_full Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title_fullStr Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title_full_unstemmed Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title_short Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains
title_sort maternal b vitamins: effects on offspring weight and dna methylation at genomically imprinted domains
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722751/
https://www.ncbi.nlm.nih.gov/pubmed/26807160
http://dx.doi.org/10.1186/s13148-016-0174-9
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