Growth hormone reduces inflammation in postmenopausal women with abdominal obesity: a 12-month, randomized, placebo-controlled trial

J Clin Endocrinol Metab. 2007 Jul;92(7):2644-7. doi: 10.1210/jc.2007-0068. Epub 2007 Apr 24.

Abstract

Context: Abdominal obesity is associated with low GH secretion, elevated circulating markers of inflammation, and increased risk of cardiovascular disease.

Objective: The objective was to study the effect of GH treatment on inflammatory markers and vascular adhesion molecules in postmenopausal women with abdominal obesity.

Design: Forty women aged 51-63 yr received GH (0.67 mg/d) in a randomized, double-blind, placebo-controlled, 12-month trial. Measurements of inflammatory markers [highly sensitive C-reactive protein (CRP), IL-6, and amyloid polypeptideA] and markers of endothelial dysfunction (soluble E-selectin, vascular adhesion molecule-1, intercellular molecule-1, and matrix metalloproteinase-9) were performed at baseline and after 6 and 12 months of treatment.

Results: After 12 months, the mean IGF sd score was 0.9 +/- 1.5 and -0.8 +/- 0.6 in the GH and placebo groups, respectively. GH treatment reduced CRP and IL-6 levels compared with placebo (P = 0.03 and P = 0.05, respectively), whereas the markers of endothelial dysfunction were unaffected. Within the GH-treated group, a reduction was shown in CRP (4.3 +/- 4 to 3.0 +/- 3 mg/liter; P < 0.05) and in IL-6 (4.4 +/- 2 to 3.3 +/- 2 ng/liter; P < 0.01). In the GH-treated group, the decrease in CRP and IL-6 correlated with a reduction in visceral adipose tissue (r = 0.7, P < 0.001 and r = 0.5, P < 0.05, respectively).

Conclusion: GH treatment in postmenopausal women with abdominal obesity reduced serum markers of systemic inflammation. Circulating markers of endothelial dysfunction were unaffected by treatment.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Fat
  • Aged
  • C-Reactive Protein / metabolism
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / immunology
  • Female
  • Human Growth Hormone / therapeutic use*
  • Humans
  • Inflammation / blood
  • Inflammation / drug therapy*
  • Interleukin-6 / blood
  • Middle Aged
  • Obesity / drug therapy*
  • Obesity / immunology*
  • Obesity / metabolism
  • Placebos
  • Postmenopause*
  • Serum Amyloid A Protein / metabolism

Substances

  • Interleukin-6
  • Placebos
  • Serum Amyloid A Protein
  • Human Growth Hormone
  • C-Reactive Protein