Background: Folate and its synthetic form folic acid function as donor of one-carbon units and have been, together with other B-vitamins, implicated in programming of epigenetic processes such as DNA methylation during early development. To what extent regulation of DNA methylation can be altered via B-vitamins later in life, and how this relates to health and disease, is not exactly known. The aim of this study was to identify effects of long-term supplementation with folic acid and vitamin B12 on genome-wide DNA methylation in elderly subjects. Results: After intervention with folic acid and vitamin B12, 162 (versus 14 in the placebo group) of the 431,312 positions were differentially methylated as compared to baseline. Comparisons of the DNA methylation changes in the participants receiving folic acid and vitamin B12 versus placebo revealed one single differentially methylated position (cg19380919) with a borderline statistical significance. However, based on the analyses of differentially methylated regions (DMRs) consisting of multiple positions, we identified 6 regions that differed statistically significantly between the intervention and placebo group. Pronounced changes were found for regions in the DIRAS3, ARMC8, and NODAL genes, implicated in carcinogenesis and early embryonic development. Conclusions: Long-term supplementation with folic acid and vitamin B12 in elderly subjects resulted in effects on DNA methylation of several genes, among which genes implicated in developmental processes.

B-vitamins, Cancer, Development, DNA methylation, Elderly, Epigenetics, Folic acid, Infinium 450k BeadChip, Intervention trial, One-carbon metabolism, Vitamin B12
dx.doi.org/10.1186/s13148-015-0154-5, hdl.handle.net/1765/85324
Clinical Epigenetics
Department of Clinical Chemistry

Kok, D.E.G, Dhonukshe-Rutten, R.A.M, Lute, C, Heil, S.G, Uitterlinden, A.G, van der Velde, N, … Steegenga, W.T. (2015). The effects of long-term daily folic acid and vitamin B12 supplementation on genome-wide DNA methylation in elderly subjects. Clinical Epigenetics, 7(1). doi:10.1186/s13148-015-0154-5