External validation of the GREAT score to predict relapse risk in Graves’ disease: results from a multicenter, retrospective study with 741 patients

Author:

Struja Tristan1,Kaeslin Marina1,Boesiger Fabienne1,Jutzi Rebecca1,Imahorn Noemi1,Kutz Alexander1,Bernasconi Luca2,Mundwiler Esther2,Mueller Beat13,Christ-Crain Mirjam34,Meienberg Fabian4,Ebrahimi Fahim4,Henzen Christoph35,Fischli Stefan5,Kraenzlin Marius34,Meier Christian34,Schuetz Philipp13

Affiliation:

1. 1Medical University DepartmentClinic for Endocrinology, Diabetes & Metabolism

2. 2Department of Laboratory MedicineKantonsspital Aarau, Aarau, Switzerland

3. 3Medical Faculty of the University of BaselBasel, Switzerland

4. 4Clinic for EndocrinologyDiabetes & Metabolism, University Hospital of Basel, Basel, Switzerland

5. 5Clinic for EndocrinologyDiabetes & Metabolism, Kantonsspital Luzern, Luzern, Switzerland

Abstract

Context First-line treatment in Graves’ disease is often done with antithyroid agents (ATD), but relapse rates remain high making definite treatment necessary. Predictors for relapse risk help guiding initial treatment decisions. Objective We aimed to externally validate the prognostic accuracy of the recently proposed Graves’ Recurrent Events After Therapy (GREAT) score to predict relapse risk in Graves’ disease. Design, setting and participants We retrospectively analyzed data (2004–2014) of patients with a first episode of Graves’ hyperthyroidism from four Swiss endocrine outpatient clinics. Main outcome measures Relapse of hyperthyroidism analyzed by multivariate Cox regression. Results Of the 741 included patients, 371 experienced a relapse (50.1%) after a mean follow-up of 25.6 months after ATD start. In univariate regression analysis, higher serum free T4, higher thyrotropin-binding inhibitor immunoglobulin (TBII), younger age and larger goiter were associated with higher relapse risk. We found a strong increase in relapse risk with more points in the GREAT score from 33.8% in patients with GREAT class I (0–1 points), 59.4% in class II (2–3 points) with a hazard ratio of 1.79 (95% CI: 1.42–2.27, P < 0.001) and 73.6% in class III (4–6 points) with a hazard ratio of 2.24 (95% CI: 1.64–3.06, P < 0.001). Conclusions Based on this retrospective analysis within a large patient population from a multicenter study, the GREAT score shows good external validity and can be used for assessing the risk for relapse in Graves’ disease, which influence the initial treatment decisions.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Reference17 articles.

1. What Is the Best Definitive Treatment for Graves’ Disease? A Systematic Review of the Existing Literature

2. Graves’ disease;Longo;New England Journal of Medicine,2016

3. Thyrotoxicosis

4. Comparative Effectiveness of Therapies for Graves' Hyperthyroidism: A Systematic Review and Network Meta-Analysis

5. Abraham P Avenell A McGeoch SC Clark LF Bevan JS. Antithyroid drug regimen for treating Graves’ hyperthyroidism. Cochrane Database of Systematic Reviews 2010 CD003420. (doi:10.1002/14651858.CD003420.pub4)

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