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dc.date.accessioned2023-12-19T16:48:04Z
dc.date.available2023-12-19T16:48:04Z
dc.date.created2023-12-18T10:28:26Z
dc.date.issued2023
dc.identifier.citationSchellhas, Laura Monasso, Giulietta S. Felix, Janine F. Jaddoe, Vincent WV Huang, Peiyuan Fernández-Barrés, Sílvia Vrijheid, Martine Pesce, Giancarlo Annesi-Maesano, Isabella Page, Christian Magnus Brantsæter, Anne Lise Bekkhus, Mona Håberg, Siri Eldevik London, Stephanie J. Munafò, Marcus R. Zuccolo, Luisa Sharp, Gemma C. . Maternal caffeine consumption during pregnancy and offspring cord blood DNA methylation: an epigenome-wide association study meta-analysis. Epigenomics. 2023
dc.identifier.urihttp://hdl.handle.net/10852/106502
dc.description.abstractBackground: Prenatal caffeine exposure may influence offspring health via DNA methylation, but no large studies have tested this. Materials & methods: Epigenome-wide association studies and differentially methylated regions in cord blood (450k or EPIC Illumina arrays) were meta-analyzed across six European cohorts (n = 3725). Differential methylation related to self-reported caffeine intake (mg/day) from coffee, tea and cola was compared with assess whether caffeine is driving effects. Results: One CpG site (cg19370043, PRRX1) was associated with caffeine and another (cg14591243, STAG1) with cola intake. A total of 12–22 differentially methylated regions were detected with limited overlap across caffeinated beverages. Conclusion: We found little evidence to support an intrauterine effect of caffeine on offspring DNA methylation. Statistical power limitations may have impacted our findings.
dc.languageEN
dc.publisherFuture Medicine Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMaternal caffeine consumption during pregnancy and offspring cord blood DNA methylation: an epigenome-wide association study meta-analysis
dc.title.alternativeENEngelskEnglishMaternal caffeine consumption during pregnancy and offspring cord blood DNA methylation: an epigenome-wide association study meta-analysis
dc.typeJournal article
dc.creator.authorSchellhas, Laura
dc.creator.authorMonasso, Giulietta S.
dc.creator.authorFelix, Janine F.
dc.creator.authorJaddoe, Vincent WV
dc.creator.authorHuang, Peiyuan
dc.creator.authorFernández-Barrés, Sílvia
dc.creator.authorVrijheid, Martine
dc.creator.authorPesce, Giancarlo
dc.creator.authorAnnesi-Maesano, Isabella
dc.creator.authorPage, Christian Magnus
dc.creator.authorBrantsæter, Anne Lise
dc.creator.authorBekkhus, Mona
dc.creator.authorHåberg, Siri Eldevik
dc.creator.authorLondon, Stephanie J.
dc.creator.authorMunafò, Marcus R.
dc.creator.authorZuccolo, Luisa
dc.creator.authorSharp, Gemma C.
cristin.unitcode185,17,5,7
cristin.unitnameHelse-, utviklings- og personlighetspsyk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2214708
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Epigenomics&rft.volume=&rft.spage=&rft.date=2023
dc.identifier.jtitleEpigenomics
dc.identifier.volume15
dc.identifier.issue22
dc.identifier.doihttps://doi.org/10.2217/epi-2023-0263
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1750-1911
dc.type.versionPublishedVersion
dc.relation.projectNFR/221097
dc.relation.projectNFR/262700
dc.relation.projectERC/268479-BREATHE


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Attribution 4.0 International
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