首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >The effect of statins on microalbuminuria, proteinuria, progression of kidney function, and all-cause mortality in patients with non-end stage chronic kidney disease: A meta-analysis
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The effect of statins on microalbuminuria, proteinuria, progression of kidney function, and all-cause mortality in patients with non-end stage chronic kidney disease: A meta-analysis

机译:他汀类药物对非结束慢性肾病患者肾功能,蛋白尿,肾功能进展,蛋白尿,肾功能的进展,以及所有导致死亡率:荟萃分析

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Conclusive evidence regarding the effect of statins on non-end stage chronic kidney disease (CKD) has not been reported previously. This meta-analysis evaluated the association between statins and microalbuminuria, proteinuria, progression, and all-cause mortality in patients with non-end stage CKD. Databases (e.g., PubMed, Embase and the Cochrane Library) were searched for randomized controlled trials (RCTs) with data on statins, microalbuminuria, proteinuria, renal health endpoints, and all-cause mortality patients with non-end stage CKD to perform this meta-analysis. The mean difference (MD) of the urine albumin excretion ratios (UAER), 24-h urine protein excretion, and risk ratios (RR) of all-cause mortality and renal health endpoints were calculated, and the results are presented with 95% confidence intervals (CI). A total of 23 RCTs with 39,419 participants were selected. The analysis demonstrated that statins statistically reduced UAER to 26.73 mu g/min [95%CI (-51.04, 2.43), Z = 2.16, P<0.05], 24-h urine protein excretion to 682.68 mg [95%CI (-886.72, -478.63), Z = 6.56, P<0.01] and decreased all-cause mortality [RR = 0.78, 95%CI (0.72, 0.84), Z = 6.08, P<0.01]. However, the analysis results did not indicate that statins reduced the events of renal health endpoints [RR = 0.96, 95%CI (0.91,1.01), Z = 1.40, P>0.05]. In summary, our study indicates that statins statistically reduced microalbuminuria, proteinuria, and clinical deaths, but statins did not effectively slow the clinical progression of non-end stage CKD. (C) 2016 Elsevier Ltd. All rights reserved.
机译:关于他汀类药物对非终末期慢性肾病(CKD)的确凿证据尚未报告。该荟萃分析评估了他汀类药物和微蛋白尿,蛋白尿,进展和全导致死亡率之间的结合,患者在非终点CKD患者中。检测数据库(例如,PUBMED,EMBASE和Cochrane库),用于随机对照试验(RCTS),其数据属于他汀类药物,微突出白蛋白尿,蛋白尿,肾健康终点,并导致死亡率与非终级CKD进行这种元-分析。计算尿白蛋白排泄比率(UAER),24-H尿蛋白排泄和风险比(RR)的平均差异(MD),并进行了所有原因死亡率和肾健康终点,结果呈现出95%的信心间隔(CI)。共选出23名参与者的23个RCT。该分析证明,统计统计学uAer至26.73μg/ min [95%Ci(-51.04,2.43),Z = 2.16,P <0.05],24-h尿蛋白排泄至682.68mg [95%CI(-886.72) ,-478.63),Z = 6.56,P <0.01]并降低全原因死亡率[RR = 0.78,95%CI(0.72,0.84),Z = 6.08,P <0.01]。然而,分析结果并未表明他汀类药物减少了肾健康终点的事件[RR = 0.96,95%CI(0.91,1.01),Z = 1.40,P> 0.05]。总之,我们的研究表明,他汀类药物统计学减少的微蛋白尿,蛋白尿和临床死亡,但他汀类药物没有有效地减缓了非终级CKD的临床进展。 (c)2016 Elsevier Ltd.保留所有权利。

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