4.6 Article

An examination of mediation by DNA methylation on birthweight differences induced by assisted reproductive technologies

Journal

CLINICAL EPIGENETICS
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13148-022-01381-w

Keywords

Assisted reproductive technology; DNA methylation; Birthweight; MoBa; MBRN

Funding

  1. Research Council of Norway through its Centres of Excellence funding scheme [262700]
  2. Research Council of Norway [320656]
  3. Norwegian Institute of Public Health (NIPH)
  4. European Research Council (ERC) under the European Union [947684]
  5. Norwegian Institute of Public Health (FHI)
  6. European Research Council (ERC) [947684] Funding Source: European Research Council (ERC)

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This study investigates the role of DNA methylation in mediating birthweight differences between children born after assisted reproductive technologies (ART) and those naturally conceived. The findings suggest that DNA methylation plays an important role in explaining the differences in birthweight according to the mode of conception.
Background Children born after assisted reproductive technologies (ART) differ in birthweight from those naturally conceived. It has been hypothesized that this might be explained by epigenetic mechanisms. We examined whether cord blood DNA methylation mediated the birthweight difference between 890 newborns conceived by ART (764 by fresh embryo transfer and 126 frozen thawed embryo transfer) and 983 naturally conceived newborns from the Norwegian Mother, Father, and Child Cohort Study (MoBa). DNA methylation was measured by the Illumina Infinium MethylationEPIC array. We conducted mediation analyses to assess whether differentially methylated CpGs mediated the differences in birthweight observed between: (1) fresh embryo transfer and natural conception and (2) frozen and fresh embryo transfer. Results We observed a difference in birthweight between fresh embryo transfer and naturally conceived offspring of - 120 g. 44% (95% confidence interval [CI] 26% to 81%) of this difference in birthweight between fresh embryo transfer and naturally conceived offspring was explained by differences in methylation levels at four CpGs near LOXL1, CDH20, and DRC1. DNA methylation differences at two CpGs near PTGS1 and RASGRP4 jointly mediated 22% (95% CI 8.1% to 50.3%) of the birthweight differences between fresh and frozen embryo transfer. Conclusion Our findings suggest that DNA methylation is an important mechanism in explaining birthweight differences according to the mode of conception. Further research should examine how gene regulation at these loci influences fetal growth.

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