Microbiome-immune-metabolic axis in the epidemic of childhood obesity: Evidence and opportunities

Obes Rev. 2020 Feb;21(2):e12963. doi: 10.1111/obr.12963. Epub 2019 Oct 30.

Abstract

Obesity epidemic responsible for increase in diabetes, heart diseases, infections and cancer shows no signs of abating. Obesity in children is also on rise, indicating the urgent need of strategies for prevention and intervention that must begin in early life. While originally posited that obesity results from the simple concept of consuming more calories, or genetics, emerging research suggests that the bacteria living in our gut (gut microbiome) and its interactions with immune cells and metabolic organs including adipose tissues (microbiome-immune-metabolic axis) play significant role in obesity development in childhood. Specifically, abnormal changes (dysbiosis) in the gut microbiome, stimulation of inflammatory cytokines, and shifts in the metabolic functions of brown adipose tissue and the browning of white adipose tissue are associated with increased obesity. Many factors from as early as gestation appear to contribute in obesity, such as maternal health, diet, antibiotic use by mother and/or child, and birth and feeding methods. Herein, using evidence from animal and human studies, we discuss how these factors impact microbiome-immune-metabolic axis and cause obesity epidemic in children, and describe the gaps in knowledge that are warranted for future research.

Keywords: childhood obesity; immune; metabolism; microbiota.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Adipose Tissue, Brown / immunology
  • Adipose Tissue, Brown / metabolism
  • Adipose Tissue, White / immunology
  • Adipose Tissue, White / metabolism
  • Child
  • Gastrointestinal Microbiome / immunology*
  • Humans
  • Pediatric Obesity / immunology*
  • Pediatric Obesity / metabolism
  • Pediatric Obesity / microbiology