Maternal genome-wide DNA methylation profiling in gestational diabetes shows distinctive disease-associated changes relative to matched healthy pregnancies

Wu, Pensee; Farrell, William E.; Haworth, Kim E.; Emes, Richard D.; Kitchen, Mark O.; Glossop, John R.; Hanna, Fahmy W.; Fryer, Anthony A.

Abstract

Several recent reports have described associations between gestational diabetes (GDM) and changes to the epigenomic landscape where the DNA samples were derived from either cord or placental sources. We employed genome-wide 450Karray analysis to determine changes to the epigenome in a unique cohort of maternal blood DNA from 11 pregnant women prior to GDM development relative to matched controls. Hierarchical clustering segregated the samples into two distinct clusters comprising GDM and healthy pregnancies. Screening identified 100 CpGs with a mean ?-value difference of ?0.2 between cases and controls. Using stringent criteria, 5 CpGs (within COPS8, PIK3R5, HAAO, CCDC124, and C5orf34 genes) demonstrated potentials to be clinical biomarkers as revealed by differential methylation in 8 of 11 women who developed GDM relative to matched controls. We identified, for the first time, maternal methylation changes prior to the onset of GDM that may prove useful as biomarkers for early therapeutic intervention.

Citation

Wu, P., Farrell, W. E., Haworth, K. E., Emes, R. D., Kitchen, M. O., Glossop, J. R., …Fryer, A. A. (2018). Maternal genome-wide DNA methylation profiling in gestational diabetes shows distinctive disease-associated changes relative to matched healthy pregnancies. Epigenetics, 13(2), 122-128. https://doi.org/10.1080/15592294.2016.1166321

• Journal Article Type: Article
• Acceptance Date: Mar 9, 2016
• Online Publication Date: Jan 25, 2018
• Publication Date: 2018-02
• Deposit Date: Oct 26, 2016
• Publicly Available Date: Jan 25, 2018
• Journal: Epigenetics
• Print ISSN: 1559-2294
• Electronic ISSN: 1559-2308
• Publisher: Taylor & Francis Open
• Peer Reviewed: Peer Reviewed
• Volume: 13
• Issue: 2
• Pages: 122-128
• DOI: https://doi.org/10.1080/15592294.2016.1166321
• Keywords: Cancer Research; Molecular Biology
• Public URL: https://nottingham-repository.worktribe.com/output/778999
• Publisher URL: http://www.tandfonline.com/doi/full/10.1080/15592294.2016.1166321