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Reproductive history and blood cell DNA methylation later in life: the Young Finns Study

BACKGROUND: Women with a history of complications of pregnancy, including hypertensive disorders, gestational diabetes or an infant fetal growth restriction or preterm birth, are at higher risk for cardiovascular disease later in life. We aimed to examine differences in maternal DNA methylation foll...

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Autores principales: Harville, Emily W., Mishra, Pashupati P., Kähönen, Mika, Raitoharju, Emma, Marttila, Saara, Raitakari, Olli, Lehtimäki, Terho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690999/
https://www.ncbi.nlm.nih.gov/pubmed/34930449
http://dx.doi.org/10.1186/s13148-021-01215-1
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author Harville, Emily W.
Mishra, Pashupati P.
Kähönen, Mika
Raitoharju, Emma
Marttila, Saara
Raitakari, Olli
Lehtimäki, Terho
author_facet Harville, Emily W.
Mishra, Pashupati P.
Kähönen, Mika
Raitoharju, Emma
Marttila, Saara
Raitakari, Olli
Lehtimäki, Terho
author_sort Harville, Emily W.
collection PubMed
description BACKGROUND: Women with a history of complications of pregnancy, including hypertensive disorders, gestational diabetes or an infant fetal growth restriction or preterm birth, are at higher risk for cardiovascular disease later in life. We aimed to examine differences in maternal DNA methylation following pregnancy complications. METHODS: Data on women participating in the Young Finns study (n = 836) were linked to the national birth registry. DNA methylation in whole blood was assessed using the Infinium Methylation EPIC BeadChip. Epigenome-wide analysis was conducted on differential CpG methylation at 850 K sites. Reproductive history was also modeled as a predictor of four epigenetic age indices. RESULTS: Fourteen significant differentially methylated sites were found associated with both history of pre-eclampsia and overall hypertensive disorders of pregnancy. No associations were found between reproductive history and any epigenetic age acceleration measure. CONCLUSIONS: Differences in epigenetic methylation profiles could represent pre-existing risk factors, or changes that occurred as a result of experiencing these complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01215-1.
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spelling pubmed-86909992021-12-23 Reproductive history and blood cell DNA methylation later in life: the Young Finns Study Harville, Emily W. Mishra, Pashupati P. Kähönen, Mika Raitoharju, Emma Marttila, Saara Raitakari, Olli Lehtimäki, Terho Clin Epigenetics Research BACKGROUND: Women with a history of complications of pregnancy, including hypertensive disorders, gestational diabetes or an infant fetal growth restriction or preterm birth, are at higher risk for cardiovascular disease later in life. We aimed to examine differences in maternal DNA methylation following pregnancy complications. METHODS: Data on women participating in the Young Finns study (n = 836) were linked to the national birth registry. DNA methylation in whole blood was assessed using the Infinium Methylation EPIC BeadChip. Epigenome-wide analysis was conducted on differential CpG methylation at 850 K sites. Reproductive history was also modeled as a predictor of four epigenetic age indices. RESULTS: Fourteen significant differentially methylated sites were found associated with both history of pre-eclampsia and overall hypertensive disorders of pregnancy. No associations were found between reproductive history and any epigenetic age acceleration measure. CONCLUSIONS: Differences in epigenetic methylation profiles could represent pre-existing risk factors, or changes that occurred as a result of experiencing these complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01215-1. BioMed Central 2021-12-20 /pmc/articles/PMC8690999/ /pubmed/34930449 http://dx.doi.org/10.1186/s13148-021-01215-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Harville, Emily W.
Mishra, Pashupati P.
Kähönen, Mika
Raitoharju, Emma
Marttila, Saara
Raitakari, Olli
Lehtimäki, Terho
Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title_full Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title_fullStr Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title_full_unstemmed Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title_short Reproductive history and blood cell DNA methylation later in life: the Young Finns Study
title_sort reproductive history and blood cell dna methylation later in life: the young finns study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690999/
https://www.ncbi.nlm.nih.gov/pubmed/34930449
http://dx.doi.org/10.1186/s13148-021-01215-1
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