Systemic inflammation in childhood obesity: circulating inflammatory mediators and activated CD14++ monocytes

Diabetologia. 2012 Oct;55(10):2800-2810. doi: 10.1007/s00125-012-2641-y. Epub 2012 Jul 18.


Aims/hypothesis: In adults, circulating inflammatory mediators and activated CD14(++) monocytes link obesity to its metabolic and cardiovascular complications. However, it is largely unknown whether these inflammatory changes already occur in childhood obesity. To survey inflammatory changes during the early stages of obesity, we performed a comprehensive analysis of circulating inflammatory mediators, monocyte populations and their function in childhood obesity.

Methods: In lean and obese children aged 6 to 16 years (n = 96), 35 circulating inflammatory mediators including adipokines were measured. Hierarchical cluster analysis of the inflammatory mediator profiles was performed to investigate associations between inflammatory mediator clusters and clinical variables. Whole-blood monocyte phenotyping and functional testing with the toll-like receptor 4 ligand, lipopolysaccharide, were also executed.

Results: First, next to leptin, the circulating mediators chemerin, tissue inhibitor of metalloproteinase 1, EGF and TNF receptor 2 were identified as novel inflammatory mediators that are increased in childhood obesity. Second, cluster analysis of the circulating mediators distinguished two obesity clusters, two leanness clusters and one mixed cluster. All clusters showed distinct inflammatory mediator profiles, together with differences in insulin sensitivity and other clinical variables. Third, childhood obesity was associated with increased CD14(++) monocyte numbers and an activated phenotype of the CD14(++) monocyte subsets.

Conclusions/interpretation: Inflammatory mediator clusters were associated with insulin resistance in obese and lean children. The activation of CD14(++) monocyte subsets, which is associated with increased development of atherosclerosis in obese adults, was also readily detected in obese children. Our results indicate that inflammatory mechanisms linking obesity to its metabolic and cardiovascular complications are already activated in childhood obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Case-Control Studies
  • Cell Count
  • Chemokines / blood
  • Child
  • Cluster Analysis
  • Comorbidity
  • Epidermal Growth Factor / blood
  • Female
  • Humans
  • Inflammation / blood*
  • Inflammation / epidemiology
  • Inflammation / pathology*
  • Inflammation Mediators / blood*
  • Intercellular Signaling Peptides and Proteins
  • Leptin / blood
  • Lipopolysaccharide Receptors / metabolism*
  • Male
  • Monocytes / immunology
  • Monocytes / pathology*
  • Obesity / blood*
  • Obesity / epidemiology
  • Obesity / pathology*
  • Receptors, Tumor Necrosis Factor, Type II / blood
  • Regression Analysis
  • Tissue Inhibitor of Metalloproteinase-1 / blood
  • Vascular Endothelial Growth Factor A / blood


  • Chemokines
  • Inflammation Mediators
  • Intercellular Signaling Peptides and Proteins
  • Leptin
  • Lipopolysaccharide Receptors
  • RARRES2 protein, human
  • Receptors, Tumor Necrosis Factor, Type II
  • Tissue Inhibitor of Metalloproteinase-1
  • Vascular Endothelial Growth Factor A
  • Epidermal Growth Factor