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瑞舒伐他汀诱导的肾病进展停滞

Rosuvastatin-induced arrest in progression of renal disease.

作者信息

Vidt Donald G, Cressman Michael D, Harris Susan, Pears John S, Hutchinson Howard G

机构信息

Cleveland Clinic Foundation, Cleveland, Ohio, USA.

出版信息

Cardiology. 2004;102(1):52-60. doi: 10.1159/000077704. Epub 2004 Apr 2.

Abstract

Preclinical and limited clinical data suggest that statins decrease the progressive decline in renal function that occurs in patients with renal disease. Pooled analysis of data obtained from a population of hyperlipidemic patients enrolled in the rosuvastatin (Crestor) clinical development program permitted assessment of its effects on renal function both early and later in the course of treatment. Study participants were initially included in controlled clinical trials that evaluated the lipid-lowering efficacy and safety of rosuvastatin when compared with placebo or other lipid-lowering agents (i.e., atorvastatin, simvastatin, pravastatin, cholestyramine, fenofibrate or extended-release niacin). The median duration of treatment with the various doses of statins in these trials was approximately 8 weeks. Following completion of a controlled clinical trial, patients were permitted to enter an open-label extension trial and received rosuvastatin treatment. These data permitted assessment of renal function in a diverse group of over 10,000 patients who received rosuvastatin in its recommended dose range (5-40 mg) for up to 3.8 years. Mean serum creatinine concentrations were lower when compared with baseline both early and later in the course of rosuvastatin treatment. In contrast, no change in mean serum creatinine was observed with placebo. Mean glomerular filtration rates (GFR) predicted from the Modification of Diet in Renal Disease (MDRD) equation were higher when compared with baseline both early and later in the course of rosuvastatin treatment. No change in GFR was observed in the placebo group. Among patients who received long-term rosuvastatin treatment (> or =96 weeks), GFR was unchanged or tended to increase, rather than decrease, when compared with baseline irrespective of age, gender, hypertensive or diabetic status, level of renal function (GFR > or =60 vs. <60 ml/min/1.73 m(2)) at entry or urine dipstick protein status prior to or during the period of treatment. These findings suggest that rosuvastatin may arrest the progression of renal disease.

摘要

临床前和有限的临床数据表明,他汀类药物可减少肾病患者肾功能的进行性下降。对参与瑞舒伐他汀(可定)临床开发项目的高脂血症患者群体所获数据进行汇总分析,从而能够评估该药在治疗早期及后期对肾功能的影响。研究参与者最初被纳入对照临床试验,这些试验比较了瑞舒伐他汀与安慰剂或其他降脂药物(即阿托伐他汀、辛伐他汀、普伐他汀、考来烯胺、非诺贝特或缓释烟酸)的降脂疗效和安全性。在这些试验中,不同剂量他汀类药物的中位治疗持续时间约为8周。对照临床试验完成后,患者可进入开放标签扩展试验并接受瑞舒伐他汀治疗。这些数据使得对超过10000名接受推荐剂量范围(5 - 40毫克)瑞舒伐他汀治疗长达3.8年的不同患者群体的肾功能进行评估成为可能。在瑞舒伐他汀治疗过程的早期和后期,平均血清肌酐浓度与基线相比均较低。相比之下,安慰剂组的平均血清肌酐未观察到变化。根据肾病饮食改良(MDRD)方程预测的平均肾小球滤过率(GFR)在瑞舒伐他汀治疗过程的早期和后期与基线相比均较高。安慰剂组的GFR未观察到变化。在接受长期瑞舒伐他汀治疗(≥96周)的患者中,无论年龄、性别、高血压或糖尿病状态、入组时的肾功能水平(GFR≥60与<60毫升/分钟/1.73平方米)或治疗期间之前或期间的尿试纸蛋白状态如何,与基线相比,GFR保持不变或有增加趋势,而非降低趋势。这些发现表明瑞舒伐他汀可能会阻止肾病的进展。

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