Graves' disease in interferon-alpha-treated and untreated patients with chronic hepatitis C virus infection

J Investig Med. 2005 Jan;53(1):26-30. doi: 10.2310/6650.2005.00002.

Abstract

An association between Graves' disease (GD) and chronic hepatitis C (C-HC) has been observed both in the presence and the absence of recombinant interferon-alpha (rIFN-alpha) treatment. rIFN-alpha-induced GD is characterized by suppressed thyroid-stimulating hormone levels; normal or elevated free triiodothyronine (FT3) and free thyroxine (FT4) values; the presence of thyroid peroxidase antibodies, antithyroglobulin antibodies, and thyroid receptor antibodies; and high iodine thyroid uptake. In contrast, GD developed during C-HC without rIFN-alpha is less clearly defined. In this study, we examined two groups of patients: group A, 28 patients with C-HC treated with rIFN-alpha who developed GD after 1 to 9 months, and group B, 10 patients with C-HC who developed GD without a previous rIFN-alpha treatment. At the time of GD, both groups started methimazole therapy; thyroid function was reevaluated after 3, 6, 9, and 12 months. Group A patients continued IFN. After 12 months, all patients of group A were euthyroid, and 21 of them (75%) had already stopped methimazole treatment, whereas all patients of group B were euthyroid and only 2 (20%) had stopped methimazole. In conclusion, the data show a better course of GD, with a more precocious and significantly higher number of recoveries in patients with rIFN-alpha-induced GD than in rIFN-alpha-unrelated disease. Further studies are needed to establish whether the two types of GD differ not only from a clinical point of view but also because of different underlying pathogenetic mechanisms.

MeSH terms

  • Antiviral Agents / therapeutic use*
  • Autoantibodies / blood
  • Female
  • Graves Disease / drug therapy
  • Graves Disease / etiology*
  • Graves Disease / pathology
  • Hepacivirus / classification
  • Hepacivirus / genetics
  • Hepatitis C, Chronic* / complications
  • Hepatitis C, Chronic* / drug therapy
  • Hepatitis C, Chronic* / pathology
  • Humans
  • Interferon Type I / therapeutic use*
  • Iodide Peroxidase / blood
  • Male
  • Methimazole / therapeutic use
  • Middle Aged
  • Receptors, Thyroid Hormone / immunology
  • Recombinant Proteins
  • Thyrotropin / blood
  • Thyroxine / analysis
  • Treatment Outcome
  • Triiodothyronine / analysis

Substances

  • Antiviral Agents
  • Autoantibodies
  • Interferon Type I
  • Receptors, Thyroid Hormone
  • Recombinant Proteins
  • anti-thyroglobulin
  • Triiodothyronine
  • Methimazole
  • Thyrotropin
  • Iodide Peroxidase
  • Thyroxine