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

Authors :
Carlsen EØ
Lee Y
Magnus P
Jugessur A
Page CM
Nustad HE
Håberg SE
Lie RT
Magnus MC
Source :
Clinical epigenetics [Clin Epigenetics] 2022 Nov 28; Vol. 14 (1), pp. 151. Date of Electronic Publication: 2022 Nov 28.
Publication Year :
2022

Abstract

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.<br />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.<br />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.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1868-7083
Volume :
14
Issue :
1
Database :
MEDLINE
Journal :
Clinical epigenetics
Publication Type :
Academic Journal
Accession number :
36443807
Full Text :
https://doi.org/10.1186/s13148-022-01381-w