Differentially methylated regions interrogated for metastable epialleles associate with offspring adiposity.
Stephanie W WaldropKatherine A SauderSierra S NiemiecKaterina J KechrisIvana V YangAnne P StarlingWei PerngDana DabeleaSarah J BorengasserPublished in: Epigenomics (2024)
Aim: Assess if cord blood differentially methylated regions (DMRs) representing human metastable epialleles (MEs) associate with offspring adiposity in 588 maternal-infant dyads from the Colorado Health Start Study. Materials & methods: DNA methylation was assessed via the Illumina 450K array (~439,500 CpG sites). Offspring adiposity was obtained via air displacement plethysmography. Linear regression modeled the association of DMRs potentially representing MEs with adiposity. Results & conclusion: We identified two potential MEs, ZFP57 , which associated with infant adiposity change and B4GALNT4 , which associated with infancy and childhood adiposity change. Nine DMRs annotating to genes that annotated to MEs associated with change in offspring adiposity (false discovery rate <0.05). Methylation of approximately 80% of DMRs identified associated with decreased change in adiposity.