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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
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
0194-911X
787-800
Murray, Robert
c3e973b5-525c-49b3-96ee-af60a666a0f4
Kitaba, Negusse
5e35ae4a-edaa-4b78-bcb6-00628c3b6e83
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
c3e973b5-525c-49b3-96ee-af60a666a0f4
Kitaba, Negusse
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Antoun, Elie
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Titcombe, Philip
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Barton, Sheila
4f674382-ca0b-44ad-9670-e71a0b134ef0
Cooper, Cyrus
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Inskip, Hazel M.
5fb4470a-9379-49b2-a533-9da8e61058b7
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.
ac435829-360f-4e0f-8220-3011b3fe1b74
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), 787-800. (doi:10.1161/HYPERTENSIONAHA.121.17396).

Record type: Article

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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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

Identifiers

Local EPrints ID: 453530
URI: http://eprints.soton.ac.uk/id/eprint/453530
ISSN: 0194-911X
PURE UUID: 1fbb22fc-a513-4b5a-b75d-b1c84c3a5753
ORCID for Negusse Kitaba: ORCID iD orcid.org/0000-0001-7518-9096
ORCID for Philip Titcombe: ORCID iD orcid.org/0000-0002-7797-8571
ORCID for Sheila Barton: ORCID iD orcid.org/0000-0003-4963-4242
ORCID for Cyrus Cooper: ORCID iD orcid.org/0000-0003-3510-0709
ORCID for Hazel M. Inskip: ORCID iD orcid.org/0000-0001-8897-1749
ORCID for Graham C. Burdge: ORCID iD orcid.org/0000-0002-7665-2967
ORCID for Karen Lillycrop: ORCID iD orcid.org/0000-0001-7350-5489
ORCID for Keith M. Godfrey: ORCID iD orcid.org/0000-0002-4643-0618
ORCID for Mark A. Hanson: ORCID iD orcid.org/0000-0002-6907-613X

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Date deposited: 19 Jan 2022 17:34
Last modified: 18 Mar 2024 03:40

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Contributors

Author: Robert Murray
Author: Negusse Kitaba ORCID iD
Author: Elie Antoun
Author: Philip Titcombe ORCID iD
Author: Sheila Barton ORCID iD
Author: Cyrus Cooper ORCID iD
Author: Hazel M. Inskip ORCID iD
Author: Pamela A. Mahon
Author: John Deanfield
Author: Julian P. Halcox
Author: Elizabeth A. Ellins
Author: Jennifer Bryant
Author: Charles Peebles
Author: Karen Lillycrop ORCID iD
Author: Mark A. Hanson ORCID iD
Author: Epi Gen Consortium

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