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Circulating intercellular adhesion molecule-1(ICAM-1) in sera of patients with Graves' disease and Hashimoto disease

J H Lee1, M A An, J S Jeon

  • 1Department of Internal Medicine, College of Medicine, Chungnam National University, Taejon, Korea.

Insights

Elevated levels of intercellular adhesion molecule-1 (ICAM-1) are linked to autoimmune thyroid diseases like Hashimoto and Graves

Area of Science:

  • Immunology
  • Endocrinology
  • Molecular Biology

Background:

  • Intercellular adhesion molecule-1 (ICAM-1) is a glycoprotein involved in immune responses.
  • ICAM-1 plays a role in inflammatory mechanisms and is expressed on thyroid cells in Hashimoto disease.
  • Soluble variants of adhesion molecules, including ICAM-1, have been reported in circulation.

Purpose of the Study:

  • To evaluate circulating ICAM-1 levels in patients with autoimmune thyroid diseases.
  • To analyze the correlation between circulating ICAM-1 and thyroid-directed autoantibodies in Graves' disease and Hashimoto disease.

Main Methods:

  • Serum samples were collected from 58 patients with autoimmune thyroid disease (28 Graves', 30 Hashimoto).
  • Circulating ICAM-1 concentrations were measured using sandwich enzyme immunoassay.
  • Correlations with thyroid autoantibodies (antithyroglobulin, antithyroperoxidase) and TBII were analyzed.

Main Results:

  • Mean serum ICAM-1 levels were significantly higher in patients with Hashimoto disease and antithyroperoxidase-positive Graves' disease compared to normal individuals.
  • Patients with antithyroperoxidase-positive Graves' disease had higher ICAM-1 than antithyroperoxidase-negative Graves' disease patients.
  • Circulating ICAM-1 showed significant positive correlations with antithyroglobulin and antithyroperoxidase antibody titers.

Conclusions:

  • High serum ICAM-1 levels are associated with autoimmune thyroid diseases, specifically Graves' disease and Hashimoto disease.
  • Circulating ICAM-1 levels positively correlate with antithyroperoxidase antibody levels in these conditions.
Abstract

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