Programming of infant neurodevelopment by maternal obesity: potential role of maternal inflammation and insulin resistance

Asia Pac J Clin Nutr. 2017 Jun;26(Suppl 1):S36-S39. doi: 10.6133/apjcn.062017.s11.

Abstract

Background and objectives: Recent studies show that maternal obesity is associated with impaired offspring neurodevelopmental outcomes. The mechanism underlying the association is unclear. However, there is evidence to suggest a role for intra-uterine exposure to inflammation and insulin resistance (IR). We aimed to determine if maternal IR and inflammation were associated to fetal neurodevelopment as indicated by fetal heart rate variability (HRV), an index of fetal cardiac autonomic nervous system development.

Methods and study design: A total of 44 healthy maternal-fetal pairs (maternal pre-pregnancy BMI distribution: n=20 normal weight, 8 overweight, 16 obese) were analyzed. We assessed maternal inflammation (plasma IL-6 and TNF-α) and IR (HOMA index). Fetal HRV, a proxy for fetal neurodevelopment, was assessed using fetal magnetocardiogram at the 36th week of pregnancy. The relationships between maternal inflammation and IR with fetal HRV (SD1 and SD2) were estimated individually by Pearson bivariate correlations.

Results: No correlations were observed between the fetal HRV components with maternal HOMA-IR and maternal plasma levels of IL-6 and TNF-α (all p<0.05). However, the negative association between maternal TNF-α level and fetal SD2 approached significance (correlation coefficient=-0.29, 95% confidence interval=-0.62,-0.03, p=0.07).

Conclusion: Maternal IR and inflammation during pregnancy were not associated with fetal cardiac autonomic nervous system development. Further studies with a larger sample size and more maternal inflammatory indicators are needed to explore these relationships.

MeSH terms

  • Adult
  • Body Mass Index
  • Central Nervous System / growth & development*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Female
  • Gene Expression Regulation
  • Heart Rate
  • Homeostasis
  • Humans
  • Infant, Newborn
  • Inflammation / complications*
  • Insulin Resistance / physiology*
  • Obesity / complications*
  • Pregnancy
  • Pregnancy Complications*
  • Prenatal Exposure Delayed Effects / pathology

Substances

  • Cytokines