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dc.contributor.authorRonkainen, Justiina
dc.contributor.authorHeiskala, Anni
dc.contributor.authorVehmeijer, Florianne O.
dc.contributor.authorLowry, Estelle
dc.contributor.authorCaramaschi, Doretta
dc.contributor.authorEstrada Gutierrez, Guadalupe
dc.contributor.authorHeiss, Jonathan A.
dc.contributor.authorHummel, Nadine
dc.contributor.authorKeikkala, Elina
dc.contributor.authorKvist, Tuomas
dc.contributor.authorKupsco, Allison
dc.contributor.authorMelton, Phillip E.
dc.contributor.authorPesce, Giancarlo
dc.contributor.authorSoomro, Munawar Hussain
dc.contributor.authorVives-Usano, Marta
dc.contributor.authorBaïz, Nour
dc.contributor.authorBinder, Elisabeth B.
dc.contributor.authorCzamara, Darina
dc.contributor.authorGuxens, Mònica
dc.contributor.authorMustaniemi, Sanna
dc.contributor.authorLondon, Stephanie J.
dc.contributor.authorRauschert, Sebastian
dc.contributor.authorVääräsmäki, Marja
dc.contributor.authorVrijheid, Martine
dc.contributor.authorZiegler, Anette-G.
dc.contributor.authorAnnesi-Maesano, Isabella
dc.contributor.authorBustamante, Mariona
dc.contributor.authorHuang, Rae-Chi
dc.contributor.authorHummel, Sandra
dc.contributor.authorJust, Allan C.
dc.contributor.authorKajantie, Eero Olavi
dc.contributor.authorLahti, Jari
dc.contributor.authorLawlor, Debbie A.
dc.contributor.authorRäikkönen, Katri
dc.contributor.authorJarvelin, Marjo-Riitta
dc.contributor.authorFelix, Janine F.
dc.contributor.authorSebert, Sylvain
dc.date.accessioned2023-09-13T08:54:26Z
dc.date.available2023-09-13T08:54:26Z
dc.date.created2021-06-24T13:01:11Z
dc.date.issued2021
dc.identifier.citationEpigenetics. 2021, 1-13.en_US
dc.identifier.issn1559-2294
dc.identifier.urihttps://hdl.handle.net/11250/3089072
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_US
dc.language.isoengen_US
dc.publisherTaylor & Francisen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleMaternal haemoglobin levels in pregnancy and child DNA methylation: a study in the pregnancy and childhood epigenetics consortiumen_US
dc.title.alternativeMaternal haemoglobin levels in pregnancy and child DNA methylation: a study in the pregnancy and childhood epigenetics consortiumen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-13en_US
dc.source.journalEpigeneticsen_US
dc.identifier.doi10.1080/15592294.2020.1864171
dc.identifier.cristin1918170
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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