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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2005-2813
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The Journal of Clinical Endocrinology & Metabolism Vol. 91, No. 9 3464-3470
Copyright © 2006 by The Endocrine Society

Thyrotropin Receptor Autoantibodies Are Independent Risk Factors for Graves’ Ophthalmopathy and Help to Predict Severity and Outcome of the Disease

Anja K. Eckstein, Marco Plicht, Hildegard Lax, Markus Neuhäuser, Klaus Mann, Sebastian Lederbogen, Christian Heckmann, Joachim Esser and Nils G. Morgenthaler

Department of Ophthalmology (A.K.E., M.P., J.E.), Institute for Medical Informatics, Biometry and Epidemiology (H.L., M.N.), and Department of Medicine, Division of Endocrinology (K.M.), University of Essen, 45122 Essen, Germany; Private Praxis Endocrinology, 45127 Essen and 42103 Wupperthal (S.L., C.H.), Germany; and Institut für Experimentelle Endokrinologie und Endokrinologisches Forschungszentrum EnForCé (N.G.M.), Charité, Universitätsmedizin Berlin, Campus Mitte, 10117 Berlin, Germany

Address all correspondence and requests for reprints to: Anja K. Eckstein, M.D., Ph.D., Department of Ophthalmology, Essen University Clinic, Hufelandstrasse 55, D-45122 Essen, Germany. E-mail: anja.eckstein{at}uni-essen.de.

Objective: The objective of this study was to examine whether TSH-receptor antibody [TSH binding inhibitory antibodies (TBII)] levels are associated with the severity of Graves’ ophthalmopathy (GO) over the entire course of the disease.

Methods and Patients: A total of 159 patients with GO were followed for 12–24 months. One year after the first symptoms of GO, all patients were classified into mild or severe GO according to their clinical manifestations. TBII were measured every 3 months after onset of GO. Receiver operating characteristic plot analysis was performed to assess the power to discriminate both patient groups by TBII (specificity >90%).

Results: TBII levels and prevalence at each time point during follow-up were significantly higher in patients with a severe course of GO compared with patients with a mild course of GO. Prognostic statements on the course of the disease were possible for about half of the GO patients at all time points (except the first). If at first presentation and at consecutive time points TBII levels were less than 5.7, 2.6, 1.5, 1.5, 1.5, and 1.5 IU/liter, the patients had a 2.3- to 15.6-fold higher chance of a mild course. If 5–8 months after GO onset and at consecutive time points TBII levels were above 8.8, 5.1, 4.8, 2.8, and 2.8 IU/liter, the patients had a 8.7- to 31.1-fold higher risk of a severe course. This relationship of TBII to the severity was independent from age and smoking.

Conclusion: Follow-up measurements of TBII allow, in half of the patients, assessment of the prognosis of GO and, therefore, could be of additional help for the disease management.




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