Fetal Sex and the Natural History of Maternal Risk of Diabetes During and After Pregnancy

J Clin Endocrinol Metab. 2015 Jul;100(7):2574-80. doi: 10.1210/jc.2015-1763. Epub 2015 May 20.

Abstract

Context: It has recently emerged that carrying a male fetus is associated with poorer maternal β-cell function in pregnancy and an increased risk of gestational diabetes mellitus (GDM). β-cell dysfunction is the central pathophysiologic defect underlying both GDM and subsequent postpartum progression to type 2 diabetes mellitus (T2DM).

Objective: This was a retrospective cohort study that aimed to determine whether fetal sex influences the natural history of maternal risk of diabetes after delivery and in a subsequent pregnancy.

Setting: The study was conducted using population-based administrative databases in Ontario, Canada.

Patients: All women with a singleton live-birth first pregnancy between April 2000 and March 2010 (n = 642 987) were included.

Exposure: Fetal sex was the exposure of interest (313 280 delivered a girl; 329 707 delivered a boy).

Main outcome measure: Development of T2DM or a second pregnancy were the main outcome measures. Glucose tolerance in each pregnancy was classified as either GDM or non-GDM.

Results: The population was followed for a median of 3.8 years. Carrying a boy yielded a higher risk of GDM in both the first pregnancy (odds ratio [OR] =1.03; 95% confidence interval [CI], 1.0002-1.054) and second pregnancy (OR =1.04, 95% CI, 1.01-1.08). For women with GDM in the first pregnancy, the likelihood of developing T2DM before a second pregnancy was higher if they delivered a girl (OR = 1.07; 95% CI, 1.01-1.12). Recurrence of GDM was not affected by fetal sex (P = .7). However, among women with a non-GDM first pregnancy while carrying a girl, having a boy in their second pregnancy predicted an increased risk of GDM (OR = 1.07, 95% CI, 1.01-1.14).

Conclusions: Fetal sex is a previously unrecognized factor that is associated with maternal diabetic risk both after delivery and in a subsequent pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Canada / epidemiology
  • Diabetes Mellitus, Type 2 / epidemiology
  • Diabetes Mellitus, Type 2 / etiology*
  • Diabetes, Gestational / epidemiology
  • Diabetes, Gestational / etiology*
  • Female
  • Fetus / physiology*
  • Humans
  • Infant, Newborn
  • Insulin-Secreting Cells / physiology
  • Male
  • Postpartum Period
  • Pregnancy
  • Retrospective Studies
  • Risk Factors
  • Sex Factors