Decreased number of circulating endothelial progenitor cells in patients with Graves' hyperthyroidism

J Endocrinol Invest. 2011 May;34(5):335-9. doi: 10.1007/BF03347455. Epub 2010 Jun 28.

Abstract

Objective: A relevant biological role of circulating endothelial progenitor cells (EPC) was recently demonstrated. EPC are generated in the bone marrow, and interact with damaged endothelium, restoring the integrity of the monolayer. Therefore, aim of the present study was to evaluate EPC in the blood of patients with untreated Graves' hyperthyroidism (GD), in whom an increased oxidative stress was observed.

Design and methods: Twenty-three patients with untreated active GD and 18 matched normal controls (NC) were included in the study. Circulating EPC were isolated from peripheral blood. Mononuclear cells were cultured with endothelial basal medium supplemented with EGM SingleQuots, and were identified by positive double staining after 7 days in culture. Circulating levels of C reactive protein, total antioxidant power, interleukin (IL)-6, IL- 18, monocyte chemoattractant protein-1, tumor necrosis facotr- α, soluble vascular cell adhesion molecule (VCAM) and intracellular adhesion molecule were evaluated by enzymelinked immunosorbent assay kit. EPC number was also evaluated in a subgroup of GD patients after restoration of euthyroidism.

Results: Systolic blood pressure resulted increased in GD patients compared with control subjects whereas diastolic blood pressure was not significantly different. Patients with GD showed an increase in circulating levels of IL-18 and VCAM-1 and a reduction of total antioxidant power (p<0.05) compared to NC. Moreover, a reduced number of EPC was observed in patients with GD compared to NC (p<0.05) which turned to NC values after restoring euthyroidism.

Conclusion: Patients with GD showed a reduction in the physiological protective mechanisms against endothelial damage, probably induced by increased inflammation and oxidative stress.

MeSH terms

  • Adult
  • Blood Pressure / physiology
  • Cells, Cultured
  • Chemokine CCL2 / blood
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism*
  • Female
  • Graves Disease / blood*
  • Graves Disease / pathology*
  • Graves Disease / physiopathology
  • Humans
  • Interleukin-18 / blood
  • Interleukin-6 / blood
  • Male
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • Tumor Necrosis Factor-alpha / blood
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Chemokine CCL2
  • Interleukin-18
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1