High Cut-off Value of a Chimeric TSH Receptor (Mc4)-based Bioassay May Improve Prediction of Relapse in Graves' Disease for 12 months
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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.
Yao P, Xie Y, Wang Y, Liang C, Huang B Front Endocrinol (Lausanne). 2024; 15:1487490.
PMID: 39669491 PMC: 11634614. DOI: 10.3389/fendo.2024.1487490.
Thyroid-Stimulatory Antibody as a Predictive Factor for Graves' Disease Relapse.
da Silva Santos T, Oliveira J, Freitas C, Couto de Carvalho A Cureus. 2022; 14(2):e22190.
PMID: 35178331 PMC: 8843073. DOI: 10.7759/cureus.22190.
The prognostic value of thyroid-stimulating immunoglobulin in the management of Graves' disease.
Zhou Y, Zhou M, Qi Y, Wang W, Chen X, Wang S Ther Adv Endocrinol Metab. 2021; 12:20420188211044943.
PMID: 34603682 PMC: 8481717. DOI: 10.1177/20420188211044943.
Antithyroid Drug Therapy for Graves' Disease and Implications for Recurrence.
Liu J, Fu J, Xu Y, Wang G Int J Endocrinol. 2017; 2017:3813540.
PMID: 28529524 PMC: 5424485. DOI: 10.1155/2017/3813540.
Giuliani C, Saji M, Bucci I, Napolitano G Front Endocrinol (Lausanne). 2016; 7:103.
PMID: 27504107 PMC: 4958915. DOI: 10.3389/fendo.2016.00103.