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Rosuvastatin-induced arrest in progression of renal disease.

机译:罗苏伐他汀诱导的肾脏疾病进展中止。

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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((R))) 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 (>/=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 >/=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.
机译: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逐步下降。对参与瑞舒伐他汀(Crestor(R))临床开发计划的高脂血症患者群体的数据进行汇总分析,可以评估其对治疗早期和后期肾功能的影响。研究参与者最初被纳入了对照临床试验,该试验评估了瑞舒伐他汀与安慰剂或其他降脂剂(即阿托伐他汀,辛伐他汀,普伐他汀,胆甾醇胺,非诺贝特或烟酸缓释剂)相比的降脂功效和安全性。在这些试验中,使用不同剂量的他汀类药物治疗的中位时间约为8周。在完成对照临床试验后,允许患者进入开放标签延伸试验并接受罗舒伐他汀治疗。这些数据可以评估10,000例接受推荐剂量范围(5-40 mg)瑞舒伐他汀长达3.8年的瑞舒伐他汀的患者的肾功能。在瑞舒伐他汀治疗的早期和后期,平均血清肌酐浓度均低于基线。相反,安慰剂组的平均血清肌酐没有变化。在瑞舒伐他汀治疗的早期和后期,根据肾脏疾病饮食调整(MDRD)方程预测的平均肾小球滤过率(GFR)均高于基线。安慰剂组未观察到GFR的变化。在接受长期瑞舒伐他汀治疗(> / = 96周)的患者中,与基线相比,无论年龄,性别,高血压或糖尿病状况,肾功能水平(GFR)如何,GFR均保持不变或趋于增加而不是降低在治疗前或治疗期间进入或尿液试纸蛋白质状态 == 60 vs. <60 ml / min / 1.73 m(2))。这些发现表明,瑞舒伐他汀可能阻止肾脏疾病的进展。

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