Huang Jing, Zhang Ji-qiang, Chen Zheng, Zhang Yan, Chen Wei-dong, Wu Xue-ping
Zhongguo Zhong Yao Za Zhi. 2015 Aug;40(15):3100-9.
To systematically evaluate the efficacy and safety of tripterygium glycosides (TG) combined with ACEI/ARB preparation in treating diabetic nephropathy stage IV. The computer retrievals were made in Cochrane Libarary, PubMed, Embase, SCI, Sinnomed, CNKI, Chinainfo and VIP, and hand retrievals were conducted for meeting and academic papers (updated to December 30, 2014), in order to collect randomized controlled trials and quasi-randomized control trials for TG combined with ACEI/ARB preparation in treating diabetic nephropathy stage IV and set the literature inclusion and elimination standards. Eligible literatures were included and evaluated according to standards in Cochrane Handbook. RevMan 5.3 and Stata 12.0 were used for a Meta-analysis. A total of 13 randomized controlled trials and quasi-randomized control trials involving 1119 patients with diabetic nephropathy were included. The Meta analysis result showed that compared with the control group, the combination group showed better effects in reducing the 24-hour urinary protein [MD = -0.84, 95% CI (-1.02, -0.66)], raising albumin [SMD = 0.98, 95% CI (0.81, 1.16)], the total efficiency [OR = 4.23, 95% CI (2.77, 6.46)] and the significant efficiency [OR = 5.35, 95% CI (2.70, 10.60)], with no statistical difference in Serum Creatinine between Both groups [MD = -0.82, 95% CI (-4.30, 2.66), P = 0.64]. However, the risk of adverse reactions increased by 7% [RD = 0.07, 95% CI (0.03, 0.12)]. The Egger's test showed no publication bias. Tripterygium Glycosides combined with ACEI/ARB in treating diabetic nephropathy stage IV is supper than the single administration of ACEI/ARB, with a good prospect in clinical application. Nevertheless, due to the small-size and low-quality samples in this study, more high-quality and large sample-size randomized controlled trials shall be conducted to verify the findings.
系统评价雷公藤多苷(TG)联合血管紧张素转换酶抑制剂(ACEI)/血管紧张素Ⅱ受体拮抗剂(ARB)制剂治疗Ⅳ期糖尿病肾病的疗效及安全性。通过计算机检索Cochrane图书馆、PubMed、Embase、SCI、SinoMed、中国知网、万方数据知识服务平台和维普资讯网,并手工检索会议及学术论文(检索时间截至2014年12月30日),收集TG联合ACEI/ARB制剂治疗Ⅳ期糖尿病肾病的随机对照试验和半随机对照试验,并制定文献纳入及排除标准。按照Cochrane手册标准纳入符合条件的文献并进行评价。采用RevMan 5.3和Stata 12.0软件进行Meta分析。共纳入13项随机对照试验和半随机对照试验,涉及1119例糖尿病肾病患者。Meta分析结果显示,与对照组比较,联合组在降低24小时尿蛋白[MD = -0.84,95%CI(-1.02,-0.66)]、提高白蛋白[SMD = 0.98,95%CI(0.81,1.16)]、总有效率[OR = 4.23,95%CI(2.77,6.46)]及显效率[OR = 5.35,95%CI(2.70,10.60)]方面效果更好,两组血清肌酐比较差异无统计学意义[MD = -0.82,95%CI(-4.30,2.66),P = 0.64]。然而,不良反应风险增加了7%[RD = 0.07,95%CI(0.03,0.12)]。Egger检验显示无发表偏倚。雷公藤多苷联合ACEI/ARB治疗Ⅳ期糖尿病肾病疗效优于单用ACEI/ARB,临床应用前景良好。但本研究样本量小、质量低,需开展更多高质量、大样本随机对照试验加以验证。