Exp Clin Endocrinol Diabetes 2014; 122(1): 1-6
DOI: 10.1055/s-0033-1358484
Article
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Changes in Graves’ Ophthalmopathy after Radioiodine and Anti-Thyroid Drug Treatment of Graves’ Disease from 2 Prospective, Randomized, Open-Label, Blinded End Point Studies

D. Y. Chen
1   Department of Nuclear Medicine of The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
,
P. F. Schneider
2   Clinic for Nuclear Medicine, University Hospital, Würzburg, Germany
,
X. S. Zhang
1   Department of Nuclear Medicine of The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
,
X. Y. Luo
3   Ophthalmology Division, Guangdong General Hospital, Guangzhou, China
,
Z. M. He
4   Department of Internal Medicine of The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
,
T. H. Chen
1   Department of Nuclear Medicine of The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
› Author Affiliations
Further Information

Publication History

received 25 July 2013
first decision 23 September 2013

accepted 02 October 2013

Publication Date:
07 November 2013 (online)

Abstract

Aims:

A significant association between radioiodine therapy (RIT) and the development or the worsening of pre-existing Graves’ ophthalmopathy (GO) has been reported. This post-hoc analysis of 2 studies attempted to describe the changes observed in pre-existing or new-onset GO following RIT with the goal of euthyroidism rather than hypothyroidism and to describe the relationship GO changes and the final outcome.

Patients and Methods:

In 2 prospective, randomized open-label blinded endpoint trials, patients received radioiodine alone; or, patients received radioiodine or antithyroid drug therapy (ATD). The severity and activity of GO were assessed during a 9–12-year follow-up. The study end points in study 1 were euthyroidism, hyperthyroidism, hypothyroidism, and changes in GO. In study 2, the end points were euthyroidism, hyperthyroidism, hypothyroidism, relapse, and changes in GO.

Results:

Both RIT and ATD were associated with worsening GO and new-onset GO. Both RIT and ATD led to similar aggravation of pre-existing GO or the development to new-onset GO. After RIT or ATD, the euthyroid patients (without levothyroxine substitution) demonstrated an improvement in GO, with 78–89% patients with preexisting GO exhibiting improvement, whereas hyperthyroid, hypothyroid and relapsed patients had worsening or new-onset GO.

Conclusions:

Thyroid function is a dominant risk factor. Thyroid function may be the most important determinant in worsening or new-onset GO in both the natural disease course and in treated patients, independent of the kind of treatment. Therefore, we recommend euthyroidism as a goal of treatment.

 
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