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Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults

Offspring of older mothers are at increased risk of adverse birth outcomes, childhood cancers, type 1 diabetes, and neurodevelopmental disorders. The underlying biologic mechanisms for most of these associations remain obscure. One possibility is that maternal aging may produce lasting changes in th...

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Autores principales: Markunas, Christina A., Wilcox, Allen J., Xu, Zongli, Joubert, Bonnie R., Harlid, Sophia, Panduri, Vijayalakshmi, Håberg, Siri E., Nystad, Wenche, London, Stephanie J., Sandler, Dale P., Lie, Rolv T., Wade, Paul A., Taylor, Jack A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934688/
https://www.ncbi.nlm.nih.gov/pubmed/27383059
http://dx.doi.org/10.1371/journal.pone.0156361
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author Markunas, Christina A.
Wilcox, Allen J.
Xu, Zongli
Joubert, Bonnie R.
Harlid, Sophia
Panduri, Vijayalakshmi
Håberg, Siri E.
Nystad, Wenche
London, Stephanie J.
Sandler, Dale P.
Lie, Rolv T.
Wade, Paul A.
Taylor, Jack A.
author_facet Markunas, Christina A.
Wilcox, Allen J.
Xu, Zongli
Joubert, Bonnie R.
Harlid, Sophia
Panduri, Vijayalakshmi
Håberg, Siri E.
Nystad, Wenche
London, Stephanie J.
Sandler, Dale P.
Lie, Rolv T.
Wade, Paul A.
Taylor, Jack A.
author_sort Markunas, Christina A.
collection PubMed
description Offspring of older mothers are at increased risk of adverse birth outcomes, childhood cancers, type 1 diabetes, and neurodevelopmental disorders. The underlying biologic mechanisms for most of these associations remain obscure. One possibility is that maternal aging may produce lasting changes in the epigenetic features of a child’s DNA. To test this, we explored the association of mothers’ age at pregnancy with methylation in her offspring, using blood samples from 890 Norwegian newborns and measuring DNA methylation at more than 450,000 CpG sites across the genome. We examined replication of a maternal-age finding in an independent group of 1062 Norwegian newborns, and then in 200 US middle-aged women. Older maternal age was significantly associated with reduced methylation at four adjacent CpGs near the 2(nd) exon of KLHL35 in newborns (p-values ranging from 3x10(-6) to 8x10(-7)). These associations were replicated in the independent set of newborns, and replicated again in women 40 to 60 years after their birth. This study provides the first example of parental age permanently affecting the epigenetic profile of offspring. While the specific functions of the affected gene are unknown, this finding opens the possibility that a mother’s age at pregnancy could affect her child’s health through epigenetic mechanisms.
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spelling pubmed-49346882016-07-18 Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults Markunas, Christina A. Wilcox, Allen J. Xu, Zongli Joubert, Bonnie R. Harlid, Sophia Panduri, Vijayalakshmi Håberg, Siri E. Nystad, Wenche London, Stephanie J. Sandler, Dale P. Lie, Rolv T. Wade, Paul A. Taylor, Jack A. PLoS One Research Article Offspring of older mothers are at increased risk of adverse birth outcomes, childhood cancers, type 1 diabetes, and neurodevelopmental disorders. The underlying biologic mechanisms for most of these associations remain obscure. One possibility is that maternal aging may produce lasting changes in the epigenetic features of a child’s DNA. To test this, we explored the association of mothers’ age at pregnancy with methylation in her offspring, using blood samples from 890 Norwegian newborns and measuring DNA methylation at more than 450,000 CpG sites across the genome. We examined replication of a maternal-age finding in an independent group of 1062 Norwegian newborns, and then in 200 US middle-aged women. Older maternal age was significantly associated with reduced methylation at four adjacent CpGs near the 2(nd) exon of KLHL35 in newborns (p-values ranging from 3x10(-6) to 8x10(-7)). These associations were replicated in the independent set of newborns, and replicated again in women 40 to 60 years after their birth. This study provides the first example of parental age permanently affecting the epigenetic profile of offspring. While the specific functions of the affected gene are unknown, this finding opens the possibility that a mother’s age at pregnancy could affect her child’s health through epigenetic mechanisms. Public Library of Science 2016-07-06 /pmc/articles/PMC4934688/ /pubmed/27383059 http://dx.doi.org/10.1371/journal.pone.0156361 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Markunas, Christina A.
Wilcox, Allen J.
Xu, Zongli
Joubert, Bonnie R.
Harlid, Sophia
Panduri, Vijayalakshmi
Håberg, Siri E.
Nystad, Wenche
London, Stephanie J.
Sandler, Dale P.
Lie, Rolv T.
Wade, Paul A.
Taylor, Jack A.
Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title_full Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title_fullStr Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title_full_unstemmed Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title_short Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults
title_sort maternal age at delivery is associated with an epigenetic signature in both newborns and adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934688/
https://www.ncbi.nlm.nih.gov/pubmed/27383059
http://dx.doi.org/10.1371/journal.pone.0156361
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