4.3 Article

Placental maternally expressed gene 3 differentially methylated region methylation profile is associated with maternal glucose concentration and newborn birthweight

Journal

JOURNAL OF DIABETES INVESTIGATION
Volume 12, Issue 6, Pages 1074-1082

Publisher

WILEY
DOI: 10.1111/jdi.13432

Keywords

Epigenetics; Gestational diabetes mellitus; Maternally expressed gene 3 differentially methylated region

Funding

  1. Nature Science Foundation of Zhejiang Province [LY20H040009, LQ20H040008]
  2. Medical Health Science and Technology Project of Zhejiang Province [2018244300]

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The study aimed to investigate the association between placental MEG3 DNA methylation profile, maternal gestational diabetes mellitus status, and newborn birthweight. Results showed significant differences in DNA methylation levels in the MEG3 differentially methylated region between gestational diabetes mellitus and control groups. Additionally, MEG3 DNA methylation levels were positively correlated with maternal fasting glucose concentrations and newborn birthweight.
Aims/Introduction Emerging evidence shows that epigenetic modifications occurring during fetal development in response to intrauterine exposures could be one of the mechanisms involved in the early determinants of adult metabolic disorders. This study aimed to investigate whether the placental maternally expressed gene 3 (MEG3) deoxyribonucleic acid (DNA) methylation profile is associated with maternal gestational diabetes mellitus status and newborn birthweight. Materials and Methods Samples for measurement were collected from 23 women with gestational diabetes mellitus and 23 healthy controls. MEG3 gene expression and DNA methylation levels were assessed using quantitative real-time polymerase chain reaction and MethylTargetTM, respectively. Pearson correlation analyses were used to examine associations between placental DNA methylation levels and clinical variables of interest. The associated results were adjusted by multivariate linear regression for maternal age, body mass index, height, gestational age and newborn sex as confounders. Results We found that the DNA methylation levels in the MEG3 differentially methylated region were significantly different between the gestational diabetes mellitus and control groups on the maternal side of the placenta (40.64 +/- 2.15 vs 38.33 +/- 2.92; P = 0.004). Furthermore, the mean MEG3 DNA methylation levels were correlated positively with maternal fasting glucose concentrations (R = 0.603, P < 0.001) and newborn birthweight (R = 0.568, P < 0.001). Conclusions The placental DNA methylation status in the MEG3 differentially methylated region was correlated with maternal glucose concentrations and newborn birthweight. These epigenetic adaptations might contribute to late-onset obesity, underlining the adverse intrauterine environment.

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