Department of Medicine, Fujian Health College, Fuzhou, Fujian Province, China.
Department of Infection, Fujian Medical University Union Hospital, Fuzhou, Fujian Province, China.
Ren Fail. 2024 Dec;46(2):2359033. doi: 10.1080/0886022X.2024.2359033. Epub 2024 Jun 5.
To determine the efficacy and safety of Astragalus combined with renin-angiotensin-aldosterone system (RAAS) blockers in treating stage III diabetic nephropathy (DN) by meta-analysis.
PubMed, Embase, Cochrane Library, Wiley, and Web of Science databases were searched for articles published between August 2007 and August 2022. Clinical studies on Astragalus combined with RAAS blockers for the treatment of stage III DN were included. Meta-analysis was performed by RevMan 5.1 and Stata 14.3 software.
A total of 32 papers were included in this meta-analysis, containing 2462 patients from randomized controlled trials, with 1244 receiving the combination treatment and 1218 solely receiving RAAS blockers. Astragalus combined with RAAS blockers yielded a significantly higher total effective rate (TER) (mean difference [MD] 3.63, 95% confidence interval [CI] 2.59-5.09) and significantly reduced urinary protein excretion rate (UPER), serum creatinine (Scr), blood urine nitrogen (BUN) and glycosylated hemoglobin (HbAlc) levels. In subgroup analysis, combining astragalus and angiotensin receptor blocker significantly lowered fasting plasma glucose (FPG) and 24 h urinary protein (24hUTP) levels, compared with the combined astragalus and angiotensin-converting enzyme inhibitor treatment. Meanwhile, the latter significantly decreased the urinary microprotein (β-MG). Importantly, the sensitivity analysis confirmed the study's stability, and publication bias was not detected for UPER, BUN, HbAlc, FPG, or β-MG. However, the TER, SCr, and 24hUTP results suggested possible publication bias.
The astragalus-RAAS blocker combination treatment is safe and improves outcomes; however, rigorous randomized, large-scale, multi-center, double-blind trials are needed to evaluate its efficacy and safety in stage III DN.
通过荟萃分析评估黄芪联合肾素-血管紧张素-醛固酮系统(RAAS)阻滞剂治疗 III 期糖尿病肾病(DN)的疗效和安全性。
检索 2007 年 8 月至 2022 年 8 月期间 PubMed、Embase、Cochrane 图书馆、Wiley 和 Web of Science 数据库中关于黄芪联合 RAAS 阻滞剂治疗 III 期 DN 的临床研究。使用 RevMan 5.1 和 Stata 14.3 软件进行荟萃分析。
本荟萃分析共纳入 32 篇文献,包含 2462 例来自随机对照试验的患者,其中 1244 例接受联合治疗,1218 例仅接受 RAAS 阻滞剂治疗。黄芪联合 RAAS 阻滞剂可显著提高总有效率(TER)(均数差 [MD] 3.63,95%置信区间 [CI] 2.59-5.09),并显著降低尿蛋白排泄率(UPER)、血清肌酐(Scr)、血尿素氮(BUN)和糖化血红蛋白(HbAlc)水平。亚组分析显示,与联合应用黄芪和血管紧张素转换酶抑制剂相比,联合应用黄芪和血管紧张素受体阻滞剂可显著降低空腹血糖(FPG)和 24 小时尿蛋白(24hUTP)水平。同时,后者可显著降低尿微量蛋白(β-MG)。重要的是,敏感性分析证实了研究的稳定性,并且未发现 UPER、BUN、HbAlc、FPG 或 β-MG 存在发表偏倚。然而,TER、Scr 和 24hUTP 的结果表明可能存在发表偏倚。
黄芪联合 RAAS 阻滞剂治疗安全有效,但需要严格的随机、大样本、多中心、双盲试验来评估其在 III 期 DN 中的疗效和安全性。