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dc.contributor.authorHaftorn, Kristine Løkås
dc.contributor.authorDenault, William Robert Paul
dc.contributor.authorLee, Yunsung
dc.contributor.authorPage, Christian Magnus
dc.contributor.authorRomanowska, Julia
dc.contributor.authorLyle, Robert
dc.contributor.authorNæss, Øyvind Erik
dc.contributor.authorKristjansson, Dana
dc.contributor.authorMagnus, Per Minor
dc.contributor.authorHåberg, Siri Eldevik
dc.contributor.authorBohlin, Jon
dc.contributor.authorJugessur, Astanand
dc.date.accessioned2024-02-01T13:32:54Z
dc.date.available2024-02-01T13:32:54Z
dc.date.created2023-03-02T14:01:43Z
dc.date.issued2023
dc.identifier.issn2399-3642
dc.identifier.urihttps://hdl.handle.net/11250/3115081
dc.description.abstractDetermining if specific cell type(s) are responsible for an association between DNA methylation (DNAm) and a given phenotype is important for understanding the biological mechanisms underlying the association. Our EWAS of gestational age (GA) in 953 newborns from the Norwegian MoBa study identified 13,660 CpGs significantly associated with GA (pBonferroni<0.05) after adjustment for cell type composition. When the CellDMC algorithm was applied to explore cell-type specific effects, 2,330 CpGs were significantly associated with GA, mostly in nucleated red blood cells [nRBCs; n = 2,030 (87%)]. Similar patterns were found in another dataset based on a different array and when applying an alternative algorithm to CellDMC called Tensor Composition Analysis (TCA). Our findings point to nRBCs as the main cell type driving the DNAm–GA association, implicating an epigenetic signature of erythropoiesis as a likely mechanism. They also explain the poor correlation observed between epigenetic age clocks for newborns and those for adults.en_US
dc.language.isoengen_US
dc.publisherNatureen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNucleated red blood cells explain most of the association between DNA methylation and gestational ageen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumber224en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1038/s42003-023-04584-w
dc.identifier.cristin2130785
dc.source.journalCommunications Biologyen_US
dc.relation.projectNorges forskningsråd: 262700en_US
dc.identifier.citationCommunications Biology. 2023, 6, 224.en_US
dc.source.volume6en_US


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