Eur J Endocrinol
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DOI: 10.1530/EJE-07-0450
European Journal of Endocrinology, Vol 158, Issue 1, 69-75
Copyright © 2008 by European Society of Endocrinology
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CLINICAL STUDIES

TSH-receptor autoimmunity in Graves' disease after therapy with anti-thyroid drugs, surgery, or radioiodine: a 5-year prospective randomized study

Peter Laurberg, Göran Wallin1, Leif Tallstedt2, Mirna Abraham-Nordling1, Göran Lundell3 and Ove Tørring4

Department of Endocrinology and Internal Medicine, Aalborg Hospital, Aarhus University Hospital, DK-9000 Aalborg, Denmark1 Department of Molecular Institution of Surgery, Karolinska University Hospital, Stockholm, Sweden2 Department of Ophthalmology, Karolinska Institutet, St Erik's Eye Hospital, Stockholm, Sweden3 Radiumhemmet, Department of General Oncology, Karolinska University Hospital, Stockholm, Sweden and 4 Department of Endocrinology and Internal Medicine and Institution of Clinical Research and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden

(Correspondence should be addressed to P Laurberg; Email: peter.laurberg{at}rn.dk)

Introduction: Autoimmunity against the TSH receptor is a key pathogenic element in Graves' disease. The autoimmune aberration may be modified by therapy of the hyperthyroidism.

Objective: To compare the effects of the common types of therapy for Graves' hyperthyroidism on TSH-receptor autoimmunity.

Methods: Patients with newly diagnosed Graves' hyperthyroidism aged 20–55 years were randomized to medical therapy, thyroid surgery, or radioiodine therapy (radioiodine was only given to patients ≥35 years of age). L-thyroxine (L-T4) was added to therapy as appropriate to keep patients euthyroid. Anti-thyroid drugs were withdrawn after 18 months of therapy. TSH-receptor antibodies (TRAb) in serum were measured before and for 5 years after the initiation of therapy.

Results: Medical therapy (n=48) and surgery (n=47) were followed by a gradual decrease in TRAb in serum, with the disappearance of TRAb in 70–80% of the patients after 18 months. Radioiodine therapy (n=36) led to a 1-year long worsening of autoimmunity against the TSH receptor, and the number of patients entering remission of TSH-receptor autoimmunity with the disappearance of TRAb from serum during the following years was considerably lower than with the other types of therapy.

Conclusion: The majority of patients with Graves' disease gradually enter remission of TSH-receptor autoimmunity during medical or after surgical therapy, with no difference between the types of therapy. Remission of TSH-receptor autoimmunity after radioiodine therapy is less common.







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