Smolders Arnaud, Kyrilli Aglaia, Constantinescu Stefan Matei, Corvilain Bernard, Daumerie Chantal, Burlacu Maria-Cristina
Eur Thyroid J. 2025 Apr 14;14(2). doi: 10.1530/ETJ-25-0039. Print 2025 Apr 1.
The optimal treatment with antithyroid drugs (ATDs) for a first episode of Graves' disease (GD) remains controversial.
Retrospective, two academic centres study of newly diagnosed GD between 1990 and 2022, treated with ATD in block-and-replace (B+R) regimen for at least 12 months and followed up for at least 1 year after ATD discontinuation or until disease relapse. Sixty patients received high-dose B+R (HD) with fixed ATD dose maintained during the study, and 60 patients received low-dose B+R (LD) with lower ATD dose adjusted during the study.
Baseline characteristics were similar in both groups. The point-prevalence of euthyroidism was not different between HD and LD (38 vs 47%, P = 0.460 at 6 months, 69 vs 82%, P = 0.194 at 12 months, 70 vs 78%, P = 0.370 at 18 months, respectively). At 18 months, 27% HD vs 38% LD (P = 0.242) had thyroid eye disease. There were no differences in the number or type of ATD-related adverse events (AE) (no AE 73 vs 78%, P = 0.707). LD received mean lower ATD dose (15.3 ± 4.2 vs 30.0 ± 0.0 mg/day, P < 0.001) and lower levothyroxine dose (72.6 ± 16.7 vs 100.6 ± 24.5 μg/day, P < 0.001). After a first course of ATD, 63% of HD patients and 60% of LD patients relapsed (P = 0.707) after a median time (interquartile range) of 11.0 (18) vs 7.0 (19) months (P = 0.109).
We observed similar relapse rates in patients with a first episode of GD receiving up to 50% less ATD and 30% less levothyroxine dose than high-dose B+R regimen.
抗甲状腺药物(ATD)对格雷夫斯病(GD)首次发作的最佳治疗方案仍存在争议。
一项回顾性研究,在两个学术中心对1990年至2022年新诊断的GD患者进行研究,这些患者采用阻断-替代(B+R)方案接受ATD治疗至少12个月,并在停用ATD后随访至少1年或直至疾病复发。60例患者接受高剂量B+R(HD)治疗,研究期间维持固定的ATD剂量,60例患者接受低剂量B+R(LD)治疗,研究期间调整较低的ATD剂量。
两组的基线特征相似。HD组和LD组甲状腺功能正常的时点患病率无差异(6个月时分别为38%对47%,P = 0.460;12个月时为69%对82%,P = 0.194;18个月时为70%对78%,P = 0.370)。18个月时,HD组甲状腺眼病的发生率为27%,LD组为38%(P = 0.242)。ATD相关不良事件(AE)的数量或类型无差异(无AE分别为73%对78%,P = 0.707)。LD组接受的ATD平均剂量较低(15.3±4.2对30.0±0.0毫克/天,P < 0.001)且左甲状腺素剂量较低(7