Endocrine Unit, Department of Medicine and Surgery, University of Insubria, Azienda Socio Sanitaria Territoriale (ASST) dei Sette Laghi, Varese, Italy.
Immunology and General Pathology Laboratory, Department of Biotechnology and Life Sciences, University of Insubria, Varese, Italy.
Front Endocrinol (Lausanne). 2022 Jun 15;13:886451. doi: 10.3389/fendo.2022.886451. eCollection 2022.
Prompt and stable control of hyperthyroidism is fundamental to avoid the detrimental effects of thyroid hormone excess, and antithyroid drugs, mainly methimazole (MMI), represent the first-line treatment for Graves' disease (GD) hyperthyroidism. Decreased serum concentrations of selenium (Se) and calcifediol (25(OH)D, VitD) have been reported in newly diagnosed GD patients in observational studies. Low Se levels might exacerbate oxidative stress by compromising the antioxidant machinery's response to reactive oxygen species, and low VitD levels might hamper the anti-inflammatory immune response. We performed a randomized controlled clinical trial (EudraCT 2017-00505011) to investigate whether Se and cholecalciferol (VitD) addition to MMI is associated with a prompter control of hyperthyroidism. Forty-two consecutive patients with newly-onset GD and marginal/insufficient Se and VitD levels were randomly assigned to treatment with either MMI monotherapy or MMI combined with Se and VitD. Se treatment was withdrawn after 180 days, while the other treatments were continued. Combination therapy resulted in a significantly greater reduction in serum FT4 concentration at 45 days (-37.9 pg/ml, CI 95%, -43.7 to -32.2 pg/ml) and 180 days (-36.5 pg/ml, CI 95%, -42 to -30.9 pg/ml) compared to MMI monotherapy (respectively: -25.7 pg/ml, CI 95%, -31.6 to -19.7 pg/ml and -22.9 pg/ml, CI 95%, -28 to -17.3 pg/ml, p 0.002). Data at 270 days confirmed this trend (-37.8 pg/ml, CI 95%, -43.6 to -32.1 pg/ml vs -24.4 pg/ml, CI 95%, -30.3 to -18.4 pg/ml). The quality of life (QoL) score was investigated by the validated "Thyroid-related Patient-Reported Outcome" questionnaire (ThyPRO). ThyPRO composite score showed a greater improvement in the intervention group at 45 days (-14.6, CI 95%, -18.8 to -10.4), 180 (-9, CI 95%, -13.9 to -4.2) and 270 days (-14.3, CI 95%, -19.5 to -9.1) compared to MMI group (respectively, -5.2, CI 95%, -9.5 to -1; -5.4, CI 95%, -10.6 to -0.2 and -3.5, CI 95%, -9 to -2.1, p 0-6 months and 6-9 months <0.05). Our results suggest that reaching optimal Se and VitD levels increases the early efficacy of MMI treatment when Se and VitD levels are suboptimal.
标题:硒和胆钙化醇治疗对 Graves 病患者甲状腺功能亢进症的影响
摘要:本研究旨在探讨在亚临床或维生素 D 不足的 Graves 病患者中,添加硒和胆钙化醇(维生素 D)治疗对甲巯咪唑(MMI)治疗 Graves 病(GD)患者甲状腺功能亢进症的疗效。
方法:研究人员采用前瞻性、随机对照临床试验,共纳入 42 例新诊断为 GD 的患者,随机分为 MMI 单药治疗组和 MMI 联合硒和胆钙化醇治疗组。治疗 180 天后停止硒治疗,而其他治疗继续进行。
结果:结果表明,与 MMI 单药治疗相比,MMI 联合硒和胆钙化醇治疗组在第 45 天和第 180 天时血清游离甲状腺素(FT4)浓度的降低更显著(分别为-37.9pg/ml,95%CI:-43.7 至-32.2pg/ml 和-36.5pg/ml,95%CI:-42 至-30.9pg/ml)(分别为-25.7pg/ml,95%CI:-31.6 至-19.7pg/ml 和-22.9pg/ml,95%CI:-28 至-17.3pg/ml,p<0.002)。在第 270 天时,这一趋势得到了进一步证实(-37.8pg/ml,95%CI:-43.6 至-32.1pg/ml 与-24.4pg/ml,95%CI:-30.3 至-18.4pg/ml)。
结论:我们的研究结果表明,在亚临床或维生素 D 不足的 Graves 病患者中,添加硒和胆钙化醇治疗可以提高 MMI 治疗的早期疗效。