Influence of maternal lifestyle and diet on perinatal DNA methylation signatures associated with childhood arterial stiffness at 8 to 9 years
Influence of maternal lifestyle and diet on perinatal DNA methylation signatures associated with childhood arterial stiffness at 8 to 9 years
Increases in aortic pulse wave velocity, a measure of arterial stiffness, can lead to elevated systolic blood pressure and increased cardiac afterload in adulthood. These changes are detectable in childhood and potentially originate in utero, where an adverse early life environment can alter DNA methylation patterns detectable at birth. Here, analysis of epigenome-wide methylation patterns using umbilical cord blood DNA from 470 participants in the Southampton’s Women’s Survey identified differential methylation patterns associated with systolic blood pressure, pulse pressure, arterial distensibility, and descending aorta pulse wave velocity measured by magnetic resonance imaging at 8 to 9 years. Perinatal methylation levels at 16 CpG loci were associated with descending aorta pulse wave velocity, with identified CpG sites enriched in pathways involved in DNA repair (P=9.03×10−11). The most significant association was with cg20793626 methylation (within protein phosphatase, Mg2+/Mn2+ dependent 1D; β=−0.05 m/s/1% methylation change, [95% CI, −0.09 to −0.02]). Genetic variation was also examined but had a minor influence on these observations. Eight pulse wave velocity-linked dmCpGs were associated with prenatal modifiable risk factors, with cg08509237 methylation (within palmitoyl-protein thioesterase-2) associated with maternal oily fish consumption in early and late pregnancy. Lower oily fish consumption in early pregnancy modified the relationship between methylation and pulse wave velocity, with lower consumption strengthening the association between cg08509237 methylation and increased pulse wave velocity. In conclusion, measurement of perinatal DNA methylation signatures has utility in identifying infants who might benefit from preventive interventions to reduce risk of later cardiovascular disease, and modifiable maternal factors can reduce this risk in the child.
Aorta, Blood pressure, DNA methylation, Epigenome, Genetic variation
787-800
Murray, Robert
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Kitaba, Negusse
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Antoun, Elie
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Titcombe, Philip
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Barton, Sheila
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Cooper, Cyrus
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Inskip, Hazel M.
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Burdge, Graham C.
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Mahon, Pamela A.
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Deanfield, John
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Halcox, Julian P.
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Ellins, Elizabeth A.
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Bryant, Jennifer
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Peebles, Charles
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Lillycrop, Karen
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Godfrey, Keith M.
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Hanson, Mark A.
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Consortium, Epi Gen
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September 2021
Murray, Robert
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Kitaba, Negusse
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Antoun, Elie
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Titcombe, Philip
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Barton, Sheila
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Cooper, Cyrus
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Inskip, Hazel M.
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Burdge, Graham C.
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Mahon, Pamela A.
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Deanfield, John
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Halcox, Julian P.
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Ellins, Elizabeth A.
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Bryant, Jennifer
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Peebles, Charles
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Lillycrop, Karen
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Godfrey, Keith M.
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Hanson, Mark A.
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Consortium, Epi Gen
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Murray, Robert, Kitaba, Negusse, Antoun, Elie, Titcombe, Philip, Barton, Sheila, Cooper, Cyrus, Inskip, Hazel M., Burdge, Graham C., Mahon, Pamela A., Deanfield, John, Halcox, Julian P., Ellins, Elizabeth A., Bryant, Jennifer, Peebles, Charles, Lillycrop, Karen, Godfrey, Keith M., Hanson, Mark A. and Consortium, Epi Gen
(2021)
Influence of maternal lifestyle and diet on perinatal DNA methylation signatures associated with childhood arterial stiffness at 8 to 9 years.
Hypertension, 78 (3), .
(doi:10.1161/HYPERTENSIONAHA.121.17396).
Abstract
Increases in aortic pulse wave velocity, a measure of arterial stiffness, can lead to elevated systolic blood pressure and increased cardiac afterload in adulthood. These changes are detectable in childhood and potentially originate in utero, where an adverse early life environment can alter DNA methylation patterns detectable at birth. Here, analysis of epigenome-wide methylation patterns using umbilical cord blood DNA from 470 participants in the Southampton’s Women’s Survey identified differential methylation patterns associated with systolic blood pressure, pulse pressure, arterial distensibility, and descending aorta pulse wave velocity measured by magnetic resonance imaging at 8 to 9 years. Perinatal methylation levels at 16 CpG loci were associated with descending aorta pulse wave velocity, with identified CpG sites enriched in pathways involved in DNA repair (P=9.03×10−11). The most significant association was with cg20793626 methylation (within protein phosphatase, Mg2+/Mn2+ dependent 1D; β=−0.05 m/s/1% methylation change, [95% CI, −0.09 to −0.02]). Genetic variation was also examined but had a minor influence on these observations. Eight pulse wave velocity-linked dmCpGs were associated with prenatal modifiable risk factors, with cg08509237 methylation (within palmitoyl-protein thioesterase-2) associated with maternal oily fish consumption in early and late pregnancy. Lower oily fish consumption in early pregnancy modified the relationship between methylation and pulse wave velocity, with lower consumption strengthening the association between cg08509237 methylation and increased pulse wave velocity. In conclusion, measurement of perinatal DNA methylation signatures has utility in identifying infants who might benefit from preventive interventions to reduce risk of later cardiovascular disease, and modifiable maternal factors can reduce this risk in the child.
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HYPERTENSIONAHA.121.17396
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Accepted/In Press date: 29 May 2021
e-pub ahead of print date: 19 July 2021
Published date: September 2021
Additional Information:
Funding Information:
K.M. Godfrey and G.C. Burdge have received reimbursement for speaking at conferences sponsored by companies selling nutritional products. K.A. Lillycrop and K.M. Godfrey are part of academic research programs that have received research funding from Abbott Nutrition, Nestec, Danone and BenevolentAI Bio Ltd. G.C. Burdge has received research funding from Abbott Nutrition, Nestec, and Danone and has been a scientific advisor to BASF. J. Deanfield is on the speakers’ bureaus for Pfizer, Sanofi-Aventis, and AstraZeneca. J.P. Halcox is on the speakers’ bureaus for Pfizer, Merck Sharpe & Dohme, and Sanofi-Aventis. The other authors report no conflicts.
Funding Information:
This work was funded by the British Heart Foundation (RG/15/17/31749). The Southampton Women’s Survey has received funding from the Medical Research Council, Dunhill Medical Trust, British Heart Foundation, Arthritis Research UK, Food Standards Agency, National Institute for Health Research (NIHR) Southampton Biomedical Research Centre, and the European Union’s Seventh Frame-work Programme (FP7/2007–2013), project EarlyNutrition, under grant agreement 289346 and the European Union’s Horizon 2020 research and innovation programme (LIFECYCLE, grant agreement No. 733206). K.M. Godfrey is supported by the UK Medical Research Council (MC_UU_12011/4), the National Institute for Health Research (NIHR Senior Investigator [NF-SI-0515-10042], NIHR Southampton 1000DaysPlus Global Nutrition Research Group [17/63/154] and NIHR Southampton Biomedical Research Centre [IS-BRC-1215-20004]), and the European Union (Erasmus+ Programme ImpENSA 598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP).
Publisher Copyright:
© 2021 The Authors. Hypertension is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Keywords:
Aorta, Blood pressure, DNA methylation, Epigenome, Genetic variation
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Local EPrints ID: 453530
URI: http://eprints.soton.ac.uk/id/eprint/453530
ISSN: 0194-911X
PURE UUID: 1fbb22fc-a513-4b5a-b75d-b1c84c3a5753
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Date deposited: 19 Jan 2022 17:34
Last modified: 18 Mar 2024 03:40
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Author:
Robert Murray
Author:
Elie Antoun
Author:
Philip Titcombe
Author:
Pamela A. Mahon
Author:
John Deanfield
Author:
Julian P. Halcox
Author:
Elizabeth A. Ellins
Author:
Jennifer Bryant
Author:
Charles Peebles
Author:
Epi Gen Consortium
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