Markers of Oxidative Stress in Human Milk do not Differ by Maternal BMI But are Related to Infant Growth Trajectories

Matern Child Health J. 2017 Jun;21(6):1367-1376. doi: 10.1007/s10995-016-2243-2.

Abstract

Objective Obesity in adults is associated with inflammation and oxidative stress. Whether or not this phenotype is reflected in human milk (HM) composition, or may impact infant growth remains unknown. We investigated whether HM from overweight/obese (OW/Ob) mothers exhibited higher concentrations of inflammatory cytokines and markers of oxidative stress. We also correlated these bioactive components with infant growth patterns. Methods This was an observational cohort of 56 breastfeeding mothers and their infants [33 normal weight (NW) and 23 OW/Ob]. Infants were followed until 6 months of age and HM collected at 2-weeks and 4-months. Results Markers of oxidative stress, 8-hydroxy-deoxyguanosine (8OHdG) and 4-hydroxynonenol (HNE), decreased in HM over time (p < 0.001) and did not differ between NW and OW/Ob women. Concentrations of inflammatory cytokines, IL-6, IL-8, and TNF-α, were all inter-correlated (p < 0.001) but did not differ between NW and OW/Ob women. HM fat, protein, lactose, and total calories did not differ between NW and OW/Ob women. Infant growth patterns did not differ by group. In a model of infant weight-for-length-Z score trajectory, there was a significant interaction between both lactose and 8OHdG with maternal group: HM lactose and 8OHdG concentrations were both positively associated with increases in WLZ trajectory only among infants breastfed by OW/Ob mothers. Conclusions for Practice HM composition was relatively stable between NW and OW/Ob women. In exclusively breastfed infants, HM concentrations of lactose and 8OHdG, a marker of oxidative stress, may contribute to regulation of infant weight gain, especially among infants of OW/Ob women.

Keywords: Breastfeeding; Human milk composition; Infant growth; Maternal obesity; Oxidative stress.

Publication types

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

MeSH terms

  • Biomarkers / analysis*
  • Body Mass Index*
  • Breast Feeding
  • Child Development
  • Child, Preschool
  • Cohort Studies
  • Cytokines / analysis
  • Female
  • Humans
  • Infant
  • Lactation / physiology
  • Longitudinal Studies
  • Milk, Human / chemistry*
  • Mothers*
  • Obesity / metabolism
  • Obesity / physiopathology
  • Overweight / physiopathology
  • Oxidative Stress

Substances

  • Biomarkers
  • Cytokines