Li Mingzhe, Wei Bingchen, Gao Tianshu, Gao Chenghan
Internal Medicine Department, The Third Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang, China.
The First Clinical College, Liaoning University of Traditional Chinese Medicine, Shenyang, China.
Front Pharmacol. 2025 Jan 6;15:1433791. doi: 10.3389/fphar.2024.1433791. eCollection 2024.
This study aims to conduct a systematic review of the effectiveness and safety of Tripterygium Glycosides interventions in the treatment of Chinese patients with thyroid-associated orbitopathy (TAO).
A literature search was conducted using PubMed for English sources, and the CNKI, Chinese Biomedical Database, Wanfang Database, and VIP Database for Chinese sources. The search period extended from the beginning of the databases' creation to Dec. 2023. The keywords used in the search were hyperthyroidism, thyroid-related immune orbitopathy (TRIO), ophthalmopathy, and Tripterygium Glycosides. Various combinations of search terms were used, depending on the database being queried. All the trials included in the study were clinical randomized controlled trials (RCTs).
33 RCTs or quasi-RCTs that met the inclusion criteria were included. The meta-analysis included 27 RCTs. 6 RCTs were excluded from the analysis due to the absence of a control group, but they were still included in the systematic review. 27 RCTs or quasi-RCTs involving 2,134 patients were included in the meta-analysis. The TRIO patients in the treatment group received Tripterygium Glycosides in combination with Thiamazole, Prednisone, Levothyroxine sodium, or a combination of these medications. While the TRIO patients in the control group were treated with Thiamazole, Prednisone, Levothyroxine sodium, or a combination of these treatments, the meta-analysis results show that the overall effectiveness rate of the treatment group and the control group was = 0.05, I = 0.33 < 0.5 [MD = 4.45, 95% CI (3.31, 5.99), < 0.00001]. The former was significantly superior to the latter. At the same time, a risk assessment was conducted for the study of the 2 groups. The former was significantly superior to the latter. Furthermore, the clinical effectiveness rate of eyeball prominence was < 0.00001, I = 0.98 > 0.5 [MD = 2.40, 95% CI (2.28, 2.51), < 0.00001]. The clinical effectiveness rate of CAS score was < 0.00001, I = 0.89 > 0.5 [MD = 1.68, 95% CI (1.50, 1.85), < 0.00001]. The clinical effectiveness rate of FT was < 0.00001, I = 0.98 > 0.5 [MD = 0.95, 95% CI (0.81, 1.08), < 0.00001], the clinical effectiveness rate of FT was < 0.00001, I = 0.95 > 0.5 [MD = 2.12, 95% CI (1.99, 2.25), < 0.00001], and the clinical effectiveness rate of TSH was < 0.00001, I = 0.89 > 0.5 [MD = -0.19, 95% CI (-0.21, -0.17), < 0.00001].
The experience with the treatment of TAO using Tripterygium Glycosides was promising. The existing evidence suggests that treatment with Tripterygium Glycosides may be more effective in enhancing the response rate, quality of life, and FT levels compared to treatment with Prednisone, Levothyroxine sodium, and/or Thiamazole alone.
本研究旨在系统评价雷公藤多苷干预治疗中国甲状腺相关性眼病(TAO)患者的有效性和安全性。
使用PubMed检索英文文献,使用中国知网、中国生物医学数据库、万方数据库和维普数据库检索中文文献。检索时间范围从各数据库创建之初至2023年12月。检索关键词为甲状腺功能亢进症、甲状腺相关免疫性眼眶病(TRIO)、眼病和雷公藤多苷。根据所查询的数据库,使用搜索词的各种组合。纳入本研究的所有试验均为临床随机对照试验(RCT)。
纳入33项符合纳入标准的RCT或准RCT。荟萃分析纳入27项RCT。6项RCT因无对照组而被排除在分析之外,但仍纳入系统评价。荟萃分析纳入了27项RCT或准RCT,涉及2134例患者。治疗组的TRIO患者接受雷公藤多苷联合甲巯咪唑、泼尼松、左甲状腺素钠或这些药物的联合治疗。而对照组的TRIO患者接受甲巯咪唑、泼尼松、左甲状腺素钠或这些治疗方法的联合治疗,荟萃分析结果显示治疗组和对照组的总有效率为 = 0.05,I = 0.33 < 0.5 [MD = 4.45,95%CI(3.31,5.99),< 0.00001]。前者显著优于后者。同时,对两组研究进行了风险评估。前者显著优于后者。此外,眼球突出的临床有效率为 < 0.00001,I = 0.98 > 0.5 [MD = 2.40,95%CI(2.28,2.51),< 0.00001]。CAS评分的临床有效率为 < 0.00001,I = 0.89 > 0.5 [MD = 1.68,95%CI(1.50,1.85),< 0.00001]。FT的临床有效率为 < 0.00001,I = 0.98 > 0.5 [MD = 0.95,95%CI(0.81,1.08),< 0.00001],FT的临床有效率为 < 0.00001,I = 0.95 > 0.5 [MD = 2.12,95%CI(1.99,2.2),< 0.00001],TSH的临床有效率为 < 0.00001,I = 0.89 > 0.5 [MD = -0.19,95%CI(-0.21,-0.17),< 0.00001]。
雷公藤多苷治疗TAO的经验令人鼓舞。现有证据表明,与单独使用泼尼松、左甲状腺素钠和/或甲巯咪唑治疗相比,雷公藤多苷治疗在提高有效率、生活质量和FT水平方面可能更有效。