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Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy

BACKGROUND: The physiological demands of pregnancy on the maternal cardiovascular system can catapult women into a metabolic syndrome that predisposes to atherosclerosis in later life. We sought to identify the nature of the epigenomic changes associated with the increased cardiovascular disease (CV...

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Autores principales: Oudejans, Cees, Poutsma, Ankie, Michel, Omar, Mulders, Joyce, Visser, Allerdien, van Dijk, Marie, Nauta, Tessa, Bokslag, Anouk, Paulus, Walter, de Haas, Andreas, Koolwijk, Pieter, de Groot, Christianne J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752476/
https://www.ncbi.nlm.nih.gov/pubmed/26870946
http://dx.doi.org/10.1371/journal.pone.0148313
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author Oudejans, Cees
Poutsma, Ankie
Michel, Omar
Mulders, Joyce
Visser, Allerdien
van Dijk, Marie
Nauta, Tessa
Bokslag, Anouk
Paulus, Walter
de Haas, Andreas
Koolwijk, Pieter
de Groot, Christianne J. M.
author_facet Oudejans, Cees
Poutsma, Ankie
Michel, Omar
Mulders, Joyce
Visser, Allerdien
van Dijk, Marie
Nauta, Tessa
Bokslag, Anouk
Paulus, Walter
de Haas, Andreas
Koolwijk, Pieter
de Groot, Christianne J. M.
author_sort Oudejans, Cees
collection PubMed
description BACKGROUND: The physiological demands of pregnancy on the maternal cardiovascular system can catapult women into a metabolic syndrome that predisposes to atherosclerosis in later life. We sought to identify the nature of the epigenomic changes associated with the increased cardiovascular disease (CVD) risk in adult women following pre-eclampsia. FINDINGS: We assessed the genome wide epigenetic profile by methyl-C sequencing of monozygotic parous twin sister pairs discordant for a severe variant of pre-eclampsia. In the adult twin sisters at risk for CVD as a consequence of a complicated pregnancy, a set of 12 differentially methylated regions with at least 50% difference in methylation percentage and the same directional change was found to be shared between the affected twin sisters and significantly different compared to their unaffected monozygous sisters. CONCLUSION: The current epigenetic marker set will permit targeted analysis of differentially methylated regions potentially related to CVD risk in large cohorts of adult women following complicated pregnancies.
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spelling pubmed-47524762016-02-26 Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy Oudejans, Cees Poutsma, Ankie Michel, Omar Mulders, Joyce Visser, Allerdien van Dijk, Marie Nauta, Tessa Bokslag, Anouk Paulus, Walter de Haas, Andreas Koolwijk, Pieter de Groot, Christianne J. M. PLoS One Research Article BACKGROUND: The physiological demands of pregnancy on the maternal cardiovascular system can catapult women into a metabolic syndrome that predisposes to atherosclerosis in later life. We sought to identify the nature of the epigenomic changes associated with the increased cardiovascular disease (CVD) risk in adult women following pre-eclampsia. FINDINGS: We assessed the genome wide epigenetic profile by methyl-C sequencing of monozygotic parous twin sister pairs discordant for a severe variant of pre-eclampsia. In the adult twin sisters at risk for CVD as a consequence of a complicated pregnancy, a set of 12 differentially methylated regions with at least 50% difference in methylation percentage and the same directional change was found to be shared between the affected twin sisters and significantly different compared to their unaffected monozygous sisters. CONCLUSION: The current epigenetic marker set will permit targeted analysis of differentially methylated regions potentially related to CVD risk in large cohorts of adult women following complicated pregnancies. Public Library of Science 2016-02-12 /pmc/articles/PMC4752476/ /pubmed/26870946 http://dx.doi.org/10.1371/journal.pone.0148313 Text en © 2016 Oudejans et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Oudejans, Cees
Poutsma, Ankie
Michel, Omar
Mulders, Joyce
Visser, Allerdien
van Dijk, Marie
Nauta, Tessa
Bokslag, Anouk
Paulus, Walter
de Haas, Andreas
Koolwijk, Pieter
de Groot, Christianne J. M.
Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title_full Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title_fullStr Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title_full_unstemmed Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title_short Genome-Wide Identification of Epigenetic Hotspots Potentially Related to Cardiovascular Risk in Adult Women after a Complicated Pregnancy
title_sort genome-wide identification of epigenetic hotspots potentially related to cardiovascular risk in adult women after a complicated pregnancy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752476/
https://www.ncbi.nlm.nih.gov/pubmed/26870946
http://dx.doi.org/10.1371/journal.pone.0148313
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