Data

P4 Paediatric Vascular Assessment substudy

Commonwealth Scientific and Industrial Research Organisation
Ross, Jason ; Varley, Benjamin ; Wells, Jadon ; Yeh, Robyn ; Pickett, Hilda ; Roberts, Lynne ; Davis, Greg ; Henry, Amanda ; Craig, Maria ; Gow, Megan
Viewed: [[ro.stat.viewed]] Cited: [[ro.stat.cited]] Accessed: [[ro.stat.accessed]]
ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.25919/6wzx-0098&rft.title=P4 Paediatric Vascular Assessment substudy&rft.identifier=https://doi.org/10.25919/6wzx-0098&rft.publisher=Commonwealth Scientific and Industrial Research Organisation&rft.description=Preeclampsia is a hypertensive disorder of pregnancy characterised by new onset hypertension at ≥ 20 weeks’ gestation accompanied by maternal organ dysfunction and/ or fetal compromise. This hypertensive exposure in pregnancy has known long-term consequences for both the mother and child.Presently, the mechanisms for these cardiometabolic, immunological and neurodevelopmental consequences in the child aren’t well characterised, but epigenetic changes in development and premature biological aging may play a role in the development of these long-term morbidities.To investigate, we assessed genome-wide DNA methylation and biological aging in the blood of 2–5 year-old children with (n=20) or without (n=20) previous intrauterine exposure to preeclampsia. Exposure to preeclampsia was associated with 69 differentially methylated regions (DMRs) proximal to both known and novel candidate genes. Biological aging, as determined by two telomere length quantification methods and an epigenetic clock, was found to not be statistically different between the preeclampsia exposure and normotensive pregnancy groups.&rft.creator=Ross, Jason &rft.creator=Varley, Benjamin &rft.creator=Wells, Jadon &rft.creator=Yeh, Robyn &rft.creator=Pickett, Hilda &rft.creator=Roberts, Lynne &rft.creator=Davis, Greg &rft.creator=Henry, Amanda &rft.creator=Craig, Maria &rft.creator=Gow, Megan &rft.date=2025&rft.edition=v1&rft_rights=Creative Commons Attribution-Noncommercial 4.0 Licence https://creativecommons.org/licenses/by-nc/4.0/&rft_rights=Access to the data is restricted&rft_rights=All Rights (including copyright) University of New South Wales 2025.&rft_subject=DNA methylation&rft_subject=preeclampsia&rft_subject=Epigenetics (incl. genome methylation and epigenomics)&rft_subject=Genetics&rft_subject=BIOLOGICAL SCIENCES&rft_subject=Child and adolescent development&rft_subject=Applied and developmental psychology&rft_subject=PSYCHOLOGY&rft.type=dataset&rft.language=English Access the data

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Creative Commons Attribution-Noncommercial 4.0 Licence
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Access to the data is restricted

All Rights (including copyright) University of New South Wales 2025.

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Preeclampsia is a hypertensive disorder of pregnancy characterised by new onset hypertension at ≥ 20 weeks’ gestation accompanied by maternal organ dysfunction and/ or fetal compromise. This hypertensive exposure in pregnancy has known long-term consequences for both the mother and child.

Presently, the mechanisms for these cardiometabolic, immunological and neurodevelopmental consequences in the child aren’t well characterised, but epigenetic changes in development and premature biological aging may play a role in the development of these long-term morbidities.

To investigate, we assessed genome-wide DNA methylation and biological aging in the blood of 2–5 year-old children with (n=20) or without (n=20) previous intrauterine exposure to preeclampsia. Exposure to preeclampsia was associated with 69 differentially methylated regions (DMRs) proximal to both known and novel candidate genes. Biological aging, as determined by two telomere length quantification methods and an epigenetic clock, was found to not be statistically different between the preeclampsia exposure and normotensive pregnancy groups.

Available: 2025-03-03

Data time period: 2019-05-01 to 2022-12-31

This dataset is part of a larger collection

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ACN 633 798 857