Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Endocrine. 2024 May;84(2):577-588. doi: 10.1007/s12020-023-03656-5. Epub 2024 Jan 2.
In Graves' disease, administration of low-dose methimazole for more than 60 months induces higher remission rates compared with the conventional duration of 12-18 months. However, the risk of recurrence and its predictors beyond 48 months of drug withdrawal are not known. The aims of this study were to determine the risk of recurrence during 84 months after withdrawal of short- or long-term methimazole therapy and a risk stratification for recurrence of hyperthyroidism.
A total of 258 patients were treated with methimazole for a median of 18 months and randomized to discontinuation of the drug(conventional short-term group; n = 128) or continuation of the treatment up to 60-120 months(long-term group; n = 130). Patients were followed for 84 months after methimazole withdrawal. Cox proportional hazards modeling was performed to identify factors associated with relapse and develop a risk-scoring model at the time of discontinuing the treatment.
Hyperthyroidism recurred in 67 of 120(56%) of conventionally-treated patients versus 20 of 118(17%) of those who received long-term methimazole treatment, p < 0.001. Age, sex, goiter grade, triiodothyronine, thyrotropin, and thyrotropin receptor antibodies were significant predictors of recurrence in both "conventional" and "long-term" groups but free thyroxine just in the "long-term" group. The risk-scoring model had a good discrimination power (optimism corrected c-index = 0.78,95%CI = 0.73-0.82) with a range of 0-14 and sensitivity of 86% and specificity of 62% at the risk-score of eight.
A relapse-free state was achieved in 83% of patients with Graves' hyperthyroidism 84 months after cessation of long-term methimazole treatment which could be predicted by some significant predictors in a simple risk-scoring system.
与传统的 12-18 个月疗程相比,在格雷夫斯病中,低剂量甲巯咪唑治疗超过 60 个月可诱导更高的缓解率。然而,停药后 48 个月以上的复发风险及其预测因素尚不清楚。本研究的目的是确定短期或长期甲巯咪唑治疗停药后 84 个月内复发的风险,并对甲状腺功能亢进症的复发进行风险分层。
共有 258 例患者接受甲巯咪唑治疗,中位数为 18 个月,并随机分为停药组(常规短期组,n=128)或继续治疗至 60-120 个月(长期组,n=130)。在停止甲巯咪唑治疗后,患者随访 84 个月。使用 Cox 比例风险模型来确定与复发相关的因素,并在停止治疗时建立风险评分模型。
在常规治疗的 120 例患者中,有 67 例(56%)出现甲状腺功能亢进症复发,而在接受长期甲巯咪唑治疗的 118 例患者中,有 20 例(17%)复发,p<0.001。年龄、性别、甲状腺肿分级、三碘甲状腺原氨酸、促甲状腺激素和促甲状腺素受体抗体是两组患者复发的显著预测因素,但游离甲状腺素仅在长期组中是显著预测因素。风险评分模型具有良好的判别能力(校正后的 optimism c 指数为 0.78,95%CI 为 0.73-0.82),风险评分范围为 0-14,风险评分 8 时的敏感性为 86%,特异性为 62%。
在停止长期甲巯咪唑治疗后 84 个月,83%的格雷夫斯病甲状腺功能亢进症患者达到无复发状态,这可以通过一个简单的风险评分系统中的一些显著预测因素来预测。