Xu Jiamei, Ma Congyuan, Li Xuanwei, Zhang Meng, Zhu Ping
Division of Nephrology, The First College of Clinical Medical Science, China Three Gorges University, 443003, Yichang, Hubei, China.
Division of Endocrinology, The Renhe Hospital of Three Gorges University, 443003, Yichang, Hubei, China.
Wien Klin Wochenschr. 2025 Apr 22. doi: 10.1007/s00508-025-02528-4.
Recent evidence increasingly confirms the therapeutic potential of endothelin receptor antagonists (ERA) in treating non-diabetic kidney nephropathy. However, clinical data in this area remain limited. Therefore, we conducted this meta-analysis to investigate the efficacy and safety of ERAs in the treatment of non-diabetic kidney nephropathy.
Randomized controlled trials were identified through PubMed, WOS, Embase, Cochrane Library and Google scholar. The initial participant characteristics and primary outcome measures were gathered, followed by the calculation of risk ratios (RR) and 95% confidence intervals (CI). Additionally, subgroup analyses were conducted to investigate the sources of heterogeneity.
In this study, seven randomized, controlled trials (RCT) were included. The results indicated that patients in the ERAs group exhibited a greater mean reduction in the urinary protein to creatinine ratio (UPCR) (standardized mean difference, MD -28.08, 95% CI -33.59 to -22.57, p < 0.001). The number of patients experiencing either complete or partial remission from proteinuria notably increased when treated with ERAs (complete remission: odds ratio, OR = 3.14, 95% CI 2.23-4.42, p < 0.001; partial remission: OR = 3.03, 95% CI 2.33-3.96, p < 0.001). Furthermore, ERAs delayed the decline in the estimated glomerular filtration rate (eGFR, MD = 3.81, 95% CI 1.71-5.90, p < 0.001). However, the incidence of edema events slightly increased in the ERA group (OR = 1.42, 95% CI 1.04-1.93, p = 0.03).
The use of ERAs is more effective than regimens without ERAs in slowing the progression of non-diabetic nephropathy.
近期证据越来越多地证实内皮素受体拮抗剂(ERA)在治疗非糖尿病肾病方面的治疗潜力。然而,该领域的临床数据仍然有限。因此,我们进行了这项荟萃分析,以研究ERA治疗非糖尿病肾病的疗效和安全性。
通过PubMed、WOS、Embase、Cochrane图书馆和谷歌学术搜索识别随机对照试验。收集初始参与者特征和主要结局指标,随后计算风险比(RR)和95%置信区间(CI)。此外,进行亚组分析以研究异质性来源。
本研究纳入了7项随机对照试验(RCT)。结果表明,ERA组患者的尿蛋白肌酐比(UPCR)平均降低幅度更大(标准化均差,MD -28.08,95%CI -33.59至-22.57,p<0.001)。接受ERA治疗时,蛋白尿完全或部分缓解的患者数量显著增加(完全缓解:比值比,OR = 3.14,95%CI 2.23 - 4.42,p<0.001;部分缓解:OR = 3.03,95%CI 2.33 - 3.96,p<0.001)。此外,ERA延缓了估计肾小球滤过率(eGFR)的下降(MD = 3.81,95%CI 1.7至-5.90,p<0.001)。然而,ERA组水肿事件的发生率略有增加(OR = 1.42,95%CI 1.04 - 1.93,p = 0.03)。
使用ERA在减缓非糖尿病肾病进展方面比不使用ERA的方案更有效。