High cut-off value of a chimeric TSH receptor (Mc4)-based bioassay may improve prediction of relapse in Graves' disease for 12 months

Endocrine. 2015 Feb;48(1):89-95. doi: 10.1007/s12020-014-0325-8. Epub 2014 Jun 27.

Abstract

There are scarce reports regarding a functional prognostic value of thyroid-stimulating autoantibody (TSAb) levels using a thyroid-stimulating hormone receptor chimera (Mc4) in Graves' disease (GD) in iodine sufficient area. The aim of this study was to investigate whether Mc4-TSAb can predict GD remission/relapse after antithyroid drug (ATD) treatment and to compare Mc4-TSAb with a binding assay using M22 monoclonal antibody (M22-TRAb) in GD patients. We retrospectively reviewed the results of M22-TRAb and Mc4-TSAb in GD patients treated with ATD for 12 months. GD patients who underwent ATD treatment for at least 12 months were included. We compared the predictive values of M22-TRAb and Mc4-TSAb for GD remission and relapse. Of the 92 patients, 60 (65.2%) achieved remission and 32 (34.8%) relapsed within 12 months. In receiver operating characteristic analysis, there were no significant differences in the area under the curves (AUCs) between Mc4-TSAb [AUC=0.79 (95% CI 0.69-0.89)] and M22-TRAb [AUC=0.69 (95% CI 0.58-0.81)]. The optimal predictive cut-off values of M22-TRAb and Mc4-TSAb were 2.23 IU/L and 230%, respectively. At a high Mc4-TSAb cut-off, the better specificity of 85.0% and positive predictive value (PPV) of 69.0% were shown compared with those at the best cut-off for M22-TRAb. In conclusion, a high cut-off for an Mc4 assay may improve the predictive value of relapse with superior specificity and PPV compared with M22-TRAb in treated GD.

MeSH terms

  • Adult
  • Antithyroid Agents / therapeutic use
  • Biological Assay
  • Female
  • Graves Disease / diagnosis*
  • Graves Disease / drug therapy
  • Graves Disease / genetics*
  • Humans
  • Immunoglobulins, Thyroid-Stimulating / analysis
  • Male
  • Middle Aged
  • Mutant Chimeric Proteins / genetics*
  • Predictive Value of Tests
  • Prognosis
  • Receptors, Thyrotropin / genetics*
  • Recurrence
  • Retrospective Studies

Substances

  • Antithyroid Agents
  • Immunoglobulins, Thyroid-Stimulating
  • Mutant Chimeric Proteins
  • Receptors, Thyrotropin