Exp Clin Endocrinol Diabetes 2014; 122(10): 564-567
DOI: 10.1055/s-0034-1377045
Article
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

A 6-year Follow-up of a Randomized Prospective Trial Comparing Methimazole Treatment with or without Exogenous L-thyroxine in Chinese Patients with Graves’ Disease

Authors

  • X. Liu

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • W. Qiang*

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • X. Liu

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • L. Liu

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • S. Liu

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • A. Gao

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • S. Gao

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
  • B. Shi

    1   Department of Endocrinology, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center
Further Information

Publication History

received 23 February 2014
first decision 20 April 2014

accepted 21 May 2014

Publication Date:
20 August 2014 (online)

Abstract

Objective:  Antithyroid drug therapy is one of the main medical treatments for Graves’ disease. There have been conflicting reports as to whether the addition of exogenous L-thyroxine improves remission rates more than antithyroid drugs alone. This randomized, controlled and prospective clinical trial was undertaken to investigate the long-term outcome of methimazole treatment with or without exogenous L-thyroxine in Chinese patients.

Methods:  145 patients with Graves’ disease were randomly divided into 3 groups and all patients initially received 30 mg of methimazole daily for at least 1 month and then followed the titration ­regimen with or without L-thyroxine: group 1 (30 mg→20 mg→15 mg→10 mg→5 mg); group 2 (30 mg→20 mg→15 mg→10 mg+L-thyroxine→5 mg+L-thyroxine); group 3 (30 mg→20 mg→15 mg→10 mg+L-thyroxine→5 mg+L-thyroxine→2.5 mg+L-thyroxine). The drug therapy was discontinued after 5 months of the final dose.

Results:  16 out of 46 patients in group 1 (34.8%), 12 out of 47 in group 2 (25.5%) and 16 out of 52 in group 3 (30.8%) had a recurrence of Graves’ disease within 6-year follow-up after drug withdrawal. Survival Analysis showed no significant differences in the remission rates between any 2 groups, despite the remission rates in group 2 and 3 were slightly higher than that in group 1.

Conclusions:  The addition of L-thyroxine to methimazole treatment in patients with Graves’ disease neither improves nor prevents the remission or recurrence of Graves’ disease in China.

* Co-first author.


 
  • References

  • 1 Weetman AP. Graves’ disease. N Engl J Med 2000; 343: 1236-1248
  • 2 Brent GA. Clinical practice. Graves’ disease. N Engl J Med 2008; 358: 2594-2605
  • 3 Torring O, Tallstedt L, Wallin G et al. Graves’ hyperthyroidism: treatment with antithyroid drugs, surgery, or radioiodine – a prospective, randomized study. Thyroid Study Group. J Clin Endocrinol Metab 1996; 81: 2986-2993
  • 4 Boelaert K. Treatment of Graves’ disease with antithyroid drugs: current perspectives. Thyroid 2010; 20: 943-946
  • 5 Hashizume K, Ichikawa K, Sakurai A et al. Administration of thyroxine in treated Graves’ disease. Effects on the level of antibodies to thyroid-stimulating hormone receptors and on the risk of recurrence of hyperthyroidism. N Engl J Med 1991; 324: 947-953
  • 6 Tamai H, Hayaki I, Kawai K et al. Lack of effect of thyroxine administration on elevated thyroid stimulating hormone receptor antibody levels in treated Graves’ disease patients. J Clin Endocrinol Metab 1995; 80: 1481-1484
  • 7 McIver B, Rae P, Beckett G et al. Lack of effect of thyroxine in patients with Graves’ hyperthyroidism who are treated with an antithyroid drug. N Engl J Med 1996; 334: 220-224
  • 8 Rittmaster RS, Abbott EC, Douglas R et al. Effect of methimazole, with or without L-thyroxine, on remission rates in Graves’ disease. J Clin Endocrinol Metab 1998; 83: 814-818
  • 9 Glinoer D, de Nayer P, Bex M. Effects of l-thyroxine administration, TSH-receptor antibodies and smoking on the risk of recurrence in Graves’ hyperthyroidism treated with antithyroid drugs: a double-blind prospective randomized study. Eur J Endocrinol 2001; 144: 475-483
  • 10 Hoermann R, Quadbeck B, Roggenbuck U et al. Relapse of Graves’ disease after successful outcome of antithyroid drug therapy: results of a prospective randomized study on the use of levothyroxine. Thyroid 2002; 12: 1119-1128
  • 11 Wartofsky L, Glinoer D, Solomon B et al. Differences and similarities in the diagnosis and treatment of Graves’ disease in Europe, Japan, and the United States. Thyroid 1991; 1: 129-135
  • 12 Volpe R. The immunomodulatory effects of anti-thyroid drugs are mediated via actions on thyroid cells, affecting thyrocyte-immunocyte signalling: a review. Curr Pharm Des 2001; 7: 451-460
  • 13 Leger J, Gelwane G, Kaguelidou F et al. Positive impact of long-term antithyroid drug treatment on the outcome of children with Graves’ disease: national long-term cohort study. J Clin Endocrinol Metab 2012; 97: 110-119
  • 14 Laurberg P. Remission of Graves’ disease during anti-thyroid drug therapy. Time to reconsider the mechanism?. Eur J Endocrinol 2006; 155: 783-786