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  • Hjort, LineUniversity of Copenhagen,Copenhagen University Hospital (författare)

Gestational diabetes and maternal obesity are associated with epigenome-wide methylation changes in children

  • Artikel/kapitelEngelska2018

Förlag, utgivningsår, omfång ...

  • 2018-09-06
  • American Society for Clinical Investigation,2018

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:6bfcf16d-2f29-468a-942c-c6d9b3bed15b
  • https://lup.lub.lu.se/record/6bfcf16d-2f29-468a-942c-c6d9b3bed15bURI
  • https://doi.org/10.1172/jci.insight.122572DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Offspring of women with gestational diabetes mellitus (GDM) are at increased risk of developing metabolic disease, potentially mediated by epigenetic mechanisms. We recruited 608 GDM and 626 control offspring from the Danish National Birth Cohort, aged between 9 and 16 years. DNA methylation profiles were measured in peripheral blood of 93 GDM offspring and 95 controls using the Illumina HumanMethylation450 BeadChip. Pyrosequencing was performed for validation/replication of putative GDM-associated, differentially methylated CpGs in additional 905 offspring (462 GDM, 444 control offspring). We identified 76 differentially methylated CpGs in GDM offspring compared with controls in the discovery cohort (FDR, P < 0.05). Adjusting for offspring BMI did not affect the association between methylation levels and GDM status for any of the 76 CpGs. Most of these epigenetic changes were due to confounding by maternal prepregnancy BMI; however, 13 methylation changes were independently associated with maternal GDM. Three prepregnancy BMI-associated CpGs (cg00992687 and cg09452568 of ESM1 and cg14328641 of MS4A3) were validated in the replication cohort, while cg09109411 (PDE6A) was found to be associated with GDM status. The identified methylation changes may reflect developmental programming of organ disease mechanisms and/or may serve as disease biomarkers.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Martino, DavidUniversity of Melbourne,Murdoch Children's Research Institute (författare)
  • Grunnet, Louise GrothCopenhagen University Hospital (författare)
  • Naeem, HaroonMurdoch Children's Research Institute,Monash University,University of Melbourne (författare)
  • Maksimovic, JovanaMurdoch Children's Research Institute,University of Melbourne (författare)
  • Olsson, Anders HenrikCopenhagen University Hospital(Swepub:lu)med-a_o (författare)
  • Zhang, CuilinNational Institute of Child Health and Human Development (författare)
  • Ling, CharlotteLund University,Lunds universitet,Diabetes - epigenetik,Forskargrupper vid Lunds universitet,Diabetes - Epigenetics,Lund University Research Groups(Swepub:lu)endo-cl0 (författare)
  • Olsen, Sjurdur FrodiDanish Serum Institute, Copenhagen (författare)
  • Saffery, RichardUniversity of Melbourne,Murdoch Children's Research Institute (författare)
  • Vaag, Allan ArthurCopenhagen University Hospital,AstraZeneca, Sweden(Swepub:lu)med-ava (författare)
  • University of CopenhagenCopenhagen University Hospital (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:JCI Insight: American Society for Clinical Investigation3:172379-3708

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