Centre for Evidence-Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine, Beijing, China.
Front Endocrinol (Lausanne). 2023 Sep 13;14:1241962. doi: 10.3389/fendo.2023.1241962. eCollection 2023.
To evaluate the effectiveness and potential mechanism of traditional Chinese medicine Jiawei-Xiaoyao-San (JWXYS) as an adjunct or mono- therapy for antithyroid drugs (ATDs) in the treatment of hyperthyroidism.
Eight databases and three trial registries were searched from inception until May 2023. Randomized controlled trials (RCTs) were included and meta-analysis was conducted using RevMan 5.4 and Stata 14.0. The Cochrane risk of bias (ROB) tool 1.0 and GRADE tool was used for quality appraisal. The findings from case reports using mono-JWXYS and pharmacological studies were summarized in tables.
Thirteen RCTs with 979 participants were included. The majority of the included studies were assessed as high risk of bias in one ROB domain. Compared with ATDs, JWXYS plus ATDs resulted in lower free triiodothyronine (FT3) (MD = -1.31 pmol/L, 95% CI [-1.85, -0.76]; low-certainty), lower free thyroxine (MD = -3.24 pmol/L, 95% CI [-5.06, -1.42]; low-certainty), higher thyroid stimulating hormone (MD = 0.42 mIU/L, 95% CI [0.26, 0.59]; low-certainty), higher effectiveness rate of traditional Chinese medicine syndrome (RR = 1.28, 95% CI [1.08, 1.52]; low-certainty), lower goiter score (MD = -0.66, 95% CI [-1.04, -0.29]; very low-certainty), lower thyrotrophin receptor antibody (SMD = -0.44, 95% CI [-0.73, -0.16]; low-certainty) and fewer adverse events (AEs) (RR = 0.34, 95% CI [0.18, 0.67]; moderate-certainty). Compared with regular dosage of ATDs, JWXYS plus half-dose ATDs resulted in fewer AEs (RR = 0.24, 95% CI [0.10, 0.59]; low-certainty). Compared with ATDs in 1 trial, JWXYS resulted in higher FT3, lower goiter score and fewer AEs. Three case reports showed that the reasons patients sought TCM-only treatment include severe AEs and multiple relapses. Three pharmacological studies demonstrated that JWXYS restored Th17/Treg balance, lowered deiodinases activity, regulated thyroid cell proliferation and apoptosis, and alleviated liver oxidative stress in mouse or rat models.
JWXYS may enhance the effectiveness of ATDs for hyperthyroidism, particularly in relieving symptoms and reducing AEs. Mono-JWXYS is not recommended except in patients intolerant to ATDs. The findings should be interpreted with caution due to overall high risk of bias. Further pharmacological studies with more reliable models are needed.
https://www.crd.york.ac.uk/prospero/, identifier CRD42023394923.
评估加味逍遥散作为辅助或单一疗法治疗甲状腺功能亢进症的有效性和潜在机制。
从建库到 2023 年 5 月,检索了 8 个数据库和 3 个试验注册处。纳入随机对照试验(RCT),使用 RevMan 5.4 和 Stata 14.0 进行荟萃分析。使用 Cochrane 偏倚风险(ROB)工具 1.0 和 GRADE 工具进行质量评估。对使用单一加味逍遥散的病例报告和药理学研究的结果进行了总结。
纳入了 13 项 RCT,共 979 名参与者。大多数纳入的研究在一个 ROB 领域被评估为高偏倚风险。与 ATD 相比,加味逍遥散联合 ATD 可降低游离三碘甲状腺原氨酸(FT3)(MD=-1.31pmol/L,95%CI[-1.85,-0.76];低确定性)、游离甲状腺素(MD=-3.24pmol/L,95%CI[-5.06,-1.42];低确定性)、促甲状腺激素(MD=0.42mIU/L,95%CI[0.26,0.59];低确定性)、中医证候疗效(RR=1.28,95%CI[1.08,1.52];低确定性)、甲状腺肿评分(MD=-0.66,95%CI[-1.04,-0.29];极低确定性)、促甲状腺素受体抗体(SMD=-0.44,95%CI[-0.73,-0.16];低确定性)和不良反应(AE)发生率(RR=0.34,95%CI[0.18,0.67];中等确定性)降低。与 ATD 的常规剂量相比,加味逍遥散联合半剂量 ATD 可降低 AE 发生率(RR=0.24,95%CI[0.10,0.59];低确定性)。与 1 项试验中的 ATD 相比,加味逍遥散可提高 FT3、降低甲状腺肿评分和减少 AE。3 份病例报告显示,患者寻求中医治疗的原因包括严重 AE 和多次复发。3 项药理学研究表明,加味逍遥散可恢复 Th17/Treg 平衡、降低脱碘酶活性、调节甲状腺细胞增殖和凋亡、减轻小鼠或大鼠模型的肝氧化应激。
加味逍遥散可能增强 ATD 治疗甲状腺功能亢进症的疗效,特别是在缓解症状和减少 AE 方面。除非患者对 ATD 不耐受,否则不建议单独使用加味逍遥散。由于总体偏倚风险较高,因此应谨慎解释研究结果。需要进行更多具有更可靠模型的药理学研究。
https://www.crd.york.ac.uk/prospero/,标识符 CRD42023394923。