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dc.contributor.authorRonkainen, J
dc.contributor.authorHeiskala, A
dc.contributor.authorVehmeijer, FOL
dc.contributor.authorLowry, E
dc.contributor.authorCaramaschi, D
dc.contributor.authorEstrada Gutierrez, G
dc.contributor.authorHeiss, JA
dc.contributor.authorHummel, N
dc.contributor.authorKeikkala, E
dc.contributor.authorKvist, T
dc.contributor.authorKupsco, A
dc.contributor.authorMelton, PE
dc.contributor.authorPesce, G
dc.contributor.authorSoomro, MH
dc.contributor.authorVives-Usano, M
dc.contributor.authorBaiz, N
dc.contributor.authorBinder, E
dc.contributor.authorCzamara, D
dc.contributor.authorGuxens, M
dc.contributor.authorMustaniemi, S
dc.contributor.authorLondon, SJ
dc.contributor.authorRauschert, S
dc.contributor.authorVääräsmäki, M
dc.contributor.authorVrijheid, M
dc.contributor.authorZiegler, A-G
dc.contributor.authorAnnesi-Maesano, I
dc.contributor.authorBustamante, M
dc.contributor.authorHuang, R-C
dc.contributor.authorHummel, S
dc.contributor.authorJust, AC
dc.contributor.authorKajantie, E
dc.contributor.authorLahti, J
dc.contributor.authorLawlor, D
dc.contributor.authorRäikkönen, K
dc.contributor.authorJärvelin, M-R
dc.contributor.authorFelix, JF
dc.contributor.authorSebert, S
dc.date.accessioned2022-05-30T07:08:23Z
dc.date.issued2020-12-17
dc.date.updated2022-05-27T20:34:14Z
dc.description.abstractAltered maternal haemoglobin levels during pregnancy are associated with pre-clinical and clinical conditions affecting the fetus. Evidence from animal models suggests that these associations may be partially explained by differential DNA methylation in the newborn with possible long-term consequences. To test this in humans, we meta-analyzed the epigenome-wide associations of maternal haemoglobin levels during pregnancy with offspring DNA methylation in 3,967 newborn cord blood and 1,534 children and 1,962 adolescent whole-blood samples derived from 10 cohorts. DNA methylation was measured using Illumina Infinium Methylation 450K or MethylationEPIC arrays covering 450,000 and 850,000 methylation sites, respectively. There was no statistical support for the association of maternal haemoglobin levels with offspring DNA methylation either at individual methylation sites or clustered in regions. For most participants, maternal haemoglobin levels were within the normal range in the current study, whereas adverse perinatal outcomes often arise at the extremes. Thus, this study does not rule out the possibility that associations with offspring DNA methylation might be seen in studies with more extreme maternal haemoglobin levels.en_GB
dc.format.extent19-31
dc.format.mediumPrint-Electronic
dc.identifier.citationVol. 17(1), pp. 19-31en_GB
dc.identifier.doihttps://doi.org/10.1080/15592294.2020.1864171
dc.identifier.urihttp://hdl.handle.net/10871/129766
dc.language.isoenen_GB
dc.publisherTaylor & Francisen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/33331245en_GB
dc.rights© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.en_GB
dc.subjectDNA methylationen_GB
dc.subjectMaternal haemoglobinen_GB
dc.subjectdevelopmental programmingen_GB
dc.subjectpregnancyen_GB
dc.titleMaternal haemoglobin levels in pregnancy and child DNA methylation: a study in the pregnancy and childhood epigenetics consortiumen_GB
dc.typeArticleen_GB
dc.date.available2022-05-30T07:08:23Z
dc.identifier.issn1559-2294
exeter.place-of-publicationUnited States
dc.descriptionThis is the final version. Available on open access from Taylor & Francis via the DOI in this recorden_GB
dc.identifier.eissn1559-2308
dc.identifier.journalEpigeneticsen_GB
dc.relation.ispartofEpigenetics, 17(1)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2020-12-08
dc.rights.licenseCC BY-NC-ND
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2020-12-17
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-05-30T06:40:49Z
refterms.versionFCDVoR
refterms.dateFOA2022-05-30T07:08:28Z
refterms.panelAen_GB
refterms.dateFirstOnline2020-12-17


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© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
Except where otherwise noted, this item's licence is described as © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.