Zheng Huijuan, Wei Junping, Wang Liansheng, Wang Qiuhong, Zhao Jing, Chen Shuya, Wei Fan
Department of Endocrinology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, No. 5 Beixiange Street, Xicheng District, Beijing, 100053, China.
Evid Based Complement Alternat Med. 2018 Sep 26;2018:3763565. doi: 10.1155/2018/3763565. eCollection 2018.
Low selenium status is associated with increased risk of Graves' disease (GD). While several trials have discussed the efficacy of selenium supplementation for thyroid function, in GD patients, the effectiveness of selenium intake as adjuvant therapy remains unclear. In this systematic review and meta-analysis, we aimed to determine the efficacy of selenium supplementation on thyroid function in GD patients. Two reviewers searched PubMed, Web of Science, the Cochrane Central Register of Controlled Trials, and four Chinese databases for studies published up to October 31, 2017. RCTs comparing the effect of selenium supplementation on thyroid hyperfunction in GD patients on antithyroid medication to placebo were included. Serum free thyroxine (FT4), free triiodothyronine (FT3), thyrotrophic hormone receptor antibody (TRAb), and thyroid-stimulating hormone (TSH) levels were assessed. Ten trials involving 796 patients were included. Random-effects meta-analyses in weighted mean difference (WMD) were performed for 3, 6, and 9 months of supplementation and compared to placebo administration. Selenium supplementation significantly decreased FT4 (WMD=-0.86 [confidence interval (CI)-1.20 to -0.53]; =0.756; I=0.0%) and FT3 (WMD=-0.34 [CI-0.66 to -0.02]; =0.719; I=0.0%) levels at 3 months, compared to placebo administration; these findings were consistent at 6 but not 9 months. TSH levels were more elevated in the group of patients taking selenium than in the control group at 3 and 6, but not 9 months. TRAb levels decreased at 6 but not 9 months. At 6 months, patients on selenium supplementation were more likely than controls to show improved thyroid function; however, the effect disappeared at 9 months. Whether these effects correlate with clinically relevant measures remains to be demonstrated.
低硒状态与格雷夫斯病(GD)风险增加有关。虽然有几项试验讨论了补充硒对甲状腺功能的疗效,但在GD患者中,摄入硒作为辅助治疗的有效性仍不明确。在这项系统评价和荟萃分析中,我们旨在确定补充硒对GD患者甲状腺功能的疗效。两名综述作者检索了PubMed、科学网、Cochrane对照试验中央注册库以及四个中文数据库,以查找截至2017年10月31日发表的研究。纳入了比较补充硒对接受抗甲状腺药物治疗的GD患者甲状腺功能亢进与安慰剂效果的随机对照试验(RCT)。评估血清游离甲状腺素(FT4)、游离三碘甲状腺原氨酸(FT3)、促甲状腺激素受体抗体(TRAb)和促甲状腺激素(TSH)水平。纳入了涉及796例患者的10项试验。对补充3、6和9个月的加权平均差(WMD)进行随机效应荟萃分析,并与安慰剂给药进行比较。与安慰剂给药相比,补充硒在3个月时显著降低了FT4(WMD=-0.86[置信区间(CI)-1.20至-0.53];P=0.756;I²=0.0%)和FT3(WMD=-0.34[CI-0.66至-0.02];P=0.719;I²=0.0%)水平;这些结果在6个月时一致,但在9个月时不一致。在3个月和6个月时,服用硒的患者组TSH水平比对照组升高,但在9个月时没有。TRAb水平在6个月时下降,但在9个月时没有。在6个月时,补充硒的患者比对照组更有可能显示甲状腺功能改善;然而,这种效果在9个月时消失。这些效果是否与临床相关指标相关仍有待证实。