Abstract

BackgroundCountries worldwide recommend women planning pregnancy to use daily 400 µg of synthetic folic acid in the periconceptional period to prevent birth defects in children. The underlying mechanisms of this preventive effect are not clear, however, epigenetic modulation of growth processes by folic acid is hypothesized. Here, we investigated whether periconceptional maternal folic acid use and markers of global DNA methylation potential (S-adenosylmethionine and S-adenosylhomocysteine blood levels) in mothers and children affect methylation of the insulin-like growth factor 2 gene differentially methylation region (IGF2 DMR) in the child. Moreover, we tested whether the methylation of the IGF2 DMR was independently associated with birth weight.Methodology/Principal Findings IGF2 DMR methylation in 120 children aged 17 months (SD 0.3) of whom 86 mothers had used and 34 had not used folic acid periconceptionally were studied. Methylation was measured of 5 CpG dinucleotides covering the DMR using a mass spectrometry-based method. Children of mother who used folic acid had a 4.5% higher methylation of the IGF2 DMR than children who were not exposed to folic acid (49.5% vs. 47.4%; p = 0.014). IGF2 DMR methylation of the children also was associated with the S-adenosylmethionine blood level of the mother but not of the child (+1.7% methylation per SD S-adenosylmethionine; p = 0.037). Finally, we observed an inverse independent association between IGF2 DMR methylation and birth weight (−1.7% methylation per SD birthweight; p = 0.034).ConclusionsPericonceptional folic acid use is associated with epigenetic changes in IGF2 in the child that may affect intrauterine programming of growth and development with consequences for health and disease throughout life. These results indicate plasticity of IGF2 methylation by periconceptional folic acid use.

Highlights

  • Every year around 8 million children are born with a serious birth defect worldwide

  • Periconceptional folic acid use is associated with epigenetic changes in insulin-like growth factor 2 (IGF2) in the child that may affect intrauterine programming of growth and development with consequences for health and disease throughout life

  • These results indicate plasticity of IGF2 methylation by periconceptional folic acid use

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Summary

Introduction

Every year around 8 million children are born with a serious birth defect worldwide. Folate deficiency during conception up to the third month of gestation, i.e., periconceptional period, is an etiological factor in several birth defects. Randomized controlled trials have shown that periconceptional synthetic folic acid use prevents neural tube defects [1]. Periconceptional folic acid use has been reported to have adverse effects including an elevated risk of pyloric stenosis, obstructive urinary tract defects, obesity, insulin resistance and colon cancer [7,8,9]. Countries worldwide recommend women planning pregnancy to use daily 400 mg of synthetic folic acid in the periconceptional period to prevent birth defects in children. We investigated whether periconceptional maternal folic acid use and markers of global DNA methylation potential (S-adenosylmethionine and Sadenosylhomocysteine blood levels) in mothers and children affect methylation of the insulin-like growth factor 2 gene differentially methylation region (IGF2 DMR) in the child. We tested whether the methylation of the IGF2 DMR was independently associated with birth weight

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