Hyperinsulinemia acutely increases serum macrophage inhibitory cytokine-1 concentration in anorexia nervosa and obesity

Clin Endocrinol (Oxf). 2012 Jan;76(1):46-50. doi: 10.1111/j.1365-2265.2011.04139.x.

Abstract

Context: Macrophage inhibitory cytokine-1 (MIC-1) plays a role in the regulation of cellular responses to stress signals and inflammation. MIC-1 has also been implicated in mediation of tumour-induced anorexia and weight loss. Increased serum concentrations of MIC-1 were found in patients with anorexia nervosa (AN), obesity and type 2 diabetes.

Objective: To estimate serum MIC-1 concentration in women with AN and obese women, its regulation by hyperinsulinemia and relationship with insulin sensitivity.

Patients: We examined 20 women with AN, 28 healthy normal-weight female controls and 28 obese women.

Measurements: Serum MIC-1 concentration was measured in the fasting state and after 2-h euglycemic hyperinsulinemic clamp.

Results: At baseline, serum MIC-1 was higher in AN in comparison with other groups (normal-weight, P = 0·018; obese, P = 0·01). Hyperinsulinemia resulted in a significant increase in serum MIC-1 concentration in the entire study population (P < 0·001) and in AN (P < 0·001), normal-weight (P = 0·002) and obese (P < 0·001) groups analysed separately. Postclamp serum MIC-1 was still higher in AN women in comparison with other groups (normal-weight, P = 0·012; obese, P = 0·023). When normal-weight and obese women were analysed together, with the exclusion of AN group, an inverse correlation between insulin sensitivity and the change in serum MIC-1 during the clamp was observed (r = -0·27, P = 0·042).

Conclusions: Hyperinsulinemia resulted in a significant increase in serum MIC-1 in different states of adiposity. Increased serum MIC-1 in AN women might be an additional factor responsible for weight loss in this group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / blood
  • Adiponectin / metabolism
  • Adolescent
  • Adult
  • Anorexia Nervosa / blood*
  • Anorexia Nervosa / metabolism
  • Female
  • Gene Expression Regulation / physiology
  • Growth Differentiation Factor 15 / blood*
  • Growth Differentiation Factor 15 / metabolism
  • Humans
  • Hyperinsulinism / blood*
  • Hyperinsulinism / metabolism
  • Obesity / blood*
  • Obesity / metabolism
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • Adiponectin
  • GDF15 protein, human
  • Growth Differentiation Factor 15
  • Tumor Necrosis Factor-alpha