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低剂量甲氨蝶呤联合甲巯咪唑治疗Graves病患者的效果:一项随机临床试验的结果

Effects of Low-dose Methotrexate With Methimazole in Patients With Graves' Disease: Results of a Randomized Clinical Trial.

作者信息

Xie Pu, Shen Liyun, Peng Rongguang, Wang Yanqiu, Yin Qinglei, Chen Xinxin, Jin Zhou, Ning Guang, Wang Weiqing, Wang Shu, Zhou Yulin

机构信息

Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai Key Laboratory for Endocrine Tumor, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

出版信息

J Clin Endocrinol Metab. 2025 Jan 21;110(2):489-497. doi: 10.1210/clinem/dgae472.

Abstract

CONTEXT

Supplemental methotrexate (MTX) may affect the clinical course of Graves' disease (GD).

OBJECTIVE

To evaluate the efficacy of add-on MTX on medical treatment in GD.

DESIGN

Prospective, open-label, randomized supplementation controlled trial.

SETTING

Academic endocrine outpatient clinic.

PATIENTS

One hundred fifty-three untreated hyperthyroid patients with GD.

INTERVENTION

Patients received MTX 10 mg/w with methimazole (MMI) or MMI only. MTX and MMI were discontinued at months 12 to 18 in euthyroid patients.

MAIN OUTCOME MEASURES

Discontinuation rate at month 18 in each group.

RESULTS

In the MTX with MMI group, the discontinuation rate was higher than the MMI group at months 15 to 18 [50.0 vs 33.3%, P = .043, 95% confidence interval (CI) 1.020-3.922; and 55.6 vs 38.9%, P = .045, 95% CI 1.011-3.815, respectively). The decrease in thyrotropin-related antibodies (TRAb) levels in the MTX with MMI group was significant from baseline to month 6 compared to the MMI alone group [MTX + MMI 67.22% (43.12-80.32), MMI 54.85% (33.18-73.76), P = .039] and became more significant from month 9 [MTX + MMI 77.79% (62.27-88.18), MMI 69.55% (50.50-83.22), P = .035] to month 18 (P < .01 in 15-18 months). A statistically significant difference was seen between the levels of TRAb in the MTX with MMI group and the MMI group at 9 to 18 months. There were no significant differences in the levels of free T3, free T4, and TSH between the 2 groups. No serious drug-related adverse events were observed in either group (P = .771).

CONCLUSION

Supplemental MTX with MMI resulted in a higher discontinuation rate and improvement in decreased TRAb levels to homeostatic levels faster than methimazole treatment alone at months 12 to 18.

摘要

背景

补充甲氨蝶呤(MTX)可能会影响格雷夫斯病(GD)的临床病程。

目的

评估加用MTX对GD药物治疗的疗效。

设计

前瞻性、开放标签、随机补充对照试验。

地点

学术性内分泌门诊。

患者

153例未经治疗的GD甲亢患者。

干预措施

患者接受每周10mg MTX联合甲巯咪唑(MMI)治疗或仅接受MMI治疗。甲状腺功能正常的患者在12至18个月时停用MTX和MMI。

主要观察指标

每组在第18个月时的停药率。

结果

在MTX联合MMI组中,15至18个月时的停药率高于MMI组[分别为50.0%对33.3%,P = 0.043,95%置信区间(CI)1.020 - 3.922;以及55.6%对38.9%,P = 0.045,95% CI 1.011 - 3.815]。与仅使用MMI组相比,MTX联合MMI组中促甲状腺素相关抗体(TRAb)水平从基线到第6个月显著下降[MTX + MMI为67.22%(43. .12 - 80.32),MMI为54.85%(33.18 - 73.76),P = 0.039],从第9个月起更显著[MTX + MMI为77.79%(62.27 - 88.18),MMI为69.55%(50.50 - 83.22),P = 0.035],到第18个月时差异有统计学意义(15至18个月时P < 0.01)。在9至18个月时,MTX联合MMI组和MMI组的TRAb水平存在统计学显著差异。两组间游离T3、游离T4和促甲状腺激素水平无显著差异。两组均未观察到严重的药物相关不良事件(P = 0.771)。

结论

在12至18个月时,MTX联合MMI补充治疗导致的停药率更高,且与单独使用甲巯咪唑治疗相比能更快地将TRAb水平降低至稳态水平。

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