Gestational diabetes mellitus, epigenetic age and offspring metabolism

Diabet Med. 2022 Nov;39(11):e14925. doi: 10.1111/dme.14925. Epub 2022 Aug 4.

Abstract

Aims: No reports examine the relationship between in-utero exposure to gestational diabetes mellitus (GDM), offspring epigenetic age acceleration (EAA), and offspring insulin sensitivity.

Methods: Using data from a cohort study, we examined associations between GDM in-utero exposure and offspring EAA at approximately 10 years of age, using separate regression models adjusting for offspring chronological age and sex. We also examined associations between EAA with updated homeostasis model assessment of insulin sensitivity and secretion (HOMA2-S and HOMA2-β) measured at approximately 10 and 16 years of age, using mixed linear regression models accounting for repeated measures after adjustment for offspring chronological age and sex.

Results: Compared to unexposed offspring (n = 91), offspring exposed to GDM (n = 88) had greater EAA or older extrinsic age compared to chronological age (β-coefficient 2.00, 95% confidence interval [0.71, 3.28], p = 0.0025), but not greater intrinsic EAA (β-coefficient -0.07, 95% CI [-0.71, 0.57], p = 0.93). Extrinsic EAA was associated with lower insulin sensitivity (β-coefficient -0.018, 95% CI [-0.035, -0.002], p = 0.03) and greater insulin secretion (β-coefficient 0.018, 95% CI [0.006, 0.03], p = 0.003), and these associations persisted after further adjustment for measures of maternal and child adiposity. No associations were observed between intrinsic EAA and insulin sensitivity and secretion, before or after adjustment for measures of maternal and child adiposity.

Conclusions: In this study, children exposed to GDM experience greater extrinsic EAA, which is associated with lower insulin sensitivity and greater insulin secretion. Further studies are needed to determine the directionality of these associations.

Keywords: children; epigenetics; gestational diabetes mellitus; insulin resistance; insulin secretion.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adiposity
  • Child
  • Cohort Studies
  • Diabetes, Gestational* / epidemiology
  • Epigenesis, Genetic
  • Female
  • Humans
  • Insulin Resistance*
  • Obesity / complications
  • Pregnancy
  • Prenatal Exposure Delayed Effects*