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Updated: Jun 30, 2025

Methodology for Accurate Detection of Mitochondrial DNA Methylation
Published on: May 20, 2018
The one-carbon metabolism as an underlying pathway for placental DNA methylation - a systematic review
Marjolein M van Vliet1,2, Sam Schoenmakers1, Joost Gribnau2
1Department of Obstetrics and Gynaecology, Erasmus MC, Rotterdam, the Netherlands.
Insights
Parental exposures impact fetal development via epigenetic modifications like DNA methylation. Micronutrients support this process, but their direct association with placental DNA methylation requires further investigation for lifelong health implications.
Area of Science:
- Epigenetics and Developmental Biology
- Nutritional Biochemistry
- Genomics
Background:
- Epigenetic modifications, particularly DNA methylation, are crucial for mediating parental exposure effects on fetal development and long-term health.
- Micronutrients such as folate, choline, and vitamin B12 are essential for one-carbon metabolism, which directly influences DNA methylation processes.
Conclusions:
- The direct impact of one-carbon metabolism on placental DNA methylation is complex and often gene- or region-specific.
- Further research is recommended to elucidate the precise role of optimized one-carbon metabolism in DNA methylation and its implications for lifelong health.
- Placental DNA methylation influenced by one-carbon moieties presents potential avenues for novel obstetrical care strategies.
Abstract:
Epigenetic modifications, including DNA methylation, are proposed mechanisms explaining the impact of parental exposures to foetal development and lifelong health. Micronutrients including folate, choline, and vitamin B12 provide methyl groups for the one-carbon metabolism and subsequent DNA methylation processes. Placental DNA methylation changes in response to one-carbon moieties hold potential targets to improve obstetrical care. We conducted a systematic review on the associations between one-carbon metabolism and human placental DNA methylation. We included 22 studies. Findings from clinical studies with minimal ErasmusAGE quality score 5/10 (n = 15) and in vitro studies (n = 3) are summarized for different one-carbon moieties. Next, results are discussed per study approach: (1) global DNA methylation (n = 9), (2) genome-wide analyses (n = 4), and (3) gene specific (n = 14). Generally, one-carbon moieties were not associated with global methylation, although conflicting outcomes were reported specifically for choline. Using genome-wide approaches, few differentially methylated sites associated with S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), or dietary patterns. Most studies taking a gene-specific approach indicated site-specific relationships depending on studied moiety and genomic region, specifically in genes involved in growth and development including LEP, NR3C1, CRH, and PlGF; however, overlap between studies was low. Therefore, we recommend to further investigate the impact of an optimized one-carbon metabolism on DNA methylation and lifelong health.
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