Tonelli Marcello, Moyé Lemuel, Sacks Frank M, Cole Thom, Curhan Gary C
University of Alberta, Edmonton, Alberta, Canada.
J Am Soc Nephrol. 2003 Jun;14(6):1605-13. doi: 10.1097/01.asn.0000068461.45784.2f.
Limited data suggest that HMG-CoA reductase inhibitors (statins) may slow loss of renal function in individuals with chronic renal insufficiency. This study was conducted to determine whether pravastatin reduced rates of loss of renal function in people with moderate chronic renal insufficiency. This was a post hoc subgroup analysis of a randomized double-blind placebo controlled trial. Data were analyzed from the CARE study (a randomized trial of pravastatin versus placebo in 4159 participants with previous myocardial infarction and total plasma cholesterol < 240 mg/dl). Participants with estimated GFR (MDRD-GFR) < 60 ml/min per 1.73 m(2) body surface area at baseline were considered to have moderate chronic renal insufficiency. Multivariate regression was used to calculate rates of decline in MDRD-GFR for individuals receiving pravastatin and placebo, controlling for prospectively determined covariates that might influence rates of renal function loss. Change in renal function could be calculated in 3384 individuals, of whom 690 (20.4%) had MDRD-GFR < 60 ml/min per 1.73 m(2) and were eligible for inclusion. Among all individuals with MDRD-GFR < 60 ml/min per 1.73 m(2)), the MDRD-GFR decline in the pravastatin group was not significantly different from that in the placebo group (0.1 ml/min per 1.73 m(2)/yr slower; 95% CI, -0.2 to 0.4; P = 0.49). However, there was a significant stepwise inverse relation between MDRD-GFR before treatment and slowing of renal function loss with pravastatin use, with more benefit in those with lower MDRD-GFR at baseline (P = 0.04). Rate of change in MDRD-GFR in the pravastatin group was 0.6 ml/min per 1.73 m(2)/yr slower than placebo (95% CI, -0.1 to 1.2; P = 0.07) in those with MDRD-GFR < 50 ml/min, and 2.5 ml/min per 1.73 m(2)/yr slower (95% CI, 1.4 to 3.6 slower; P = 0.0001) in those with MDRD-GFR < 40 ml/min per 1.73 m(2)/yr. Pravastatin also reduced rates of renal loss to a greater extent in participants with than without proteinuria at baseline (P = 0.006). It is concluded that pravastatin may slow renal function loss in individuals with moderate to severe kidney disease, especially those with proteinuria. These findings require confirmation by a large randomized trial conducted specifically in people with chronic renal insufficiency.
有限的数据表明,HMG - CoA还原酶抑制剂(他汀类药物)可能会减缓慢性肾功能不全患者肾功能的丧失。本研究旨在确定普伐他汀是否能降低中度慢性肾功能不全患者的肾功能丧失率。这是一项对随机双盲安慰剂对照试验的事后亚组分析。数据来自CARE研究(一项在4159名既往有心肌梗死且总血浆胆固醇<240mg/dl的参与者中比较普伐他汀与安慰剂的随机试验)。基线时估计肾小球滤过率(MDRD - GFR)<60ml/min/1.73m²体表面积的参与者被认为患有中度慢性肾功能不全。采用多变量回归计算接受普伐他汀和安慰剂的个体的MDRD - GFR下降率,并对可能影响肾功能丧失率的前瞻性确定的协变量进行控制。3384名个体的肾功能变化可以计算,其中690名(20.4%)的MDRD - GFR<60ml/min/1.73m²,符合纳入条件。在所有MDRD - GFR<60ml/min/1.73m²的个体中,普伐他汀组的MDRD - GFR下降与安慰剂组无显著差异(每年减慢0.1ml/min/1.73m²;95%CI,-0.2至0.4;P = 0.49)。然而,治疗前的MDRD - GFR与使用普伐他汀减缓肾功能丧失之间存在显著的逐步负相关,基线时MDRD - GFR较低者获益更多(P = 0.04)。在MDRD - GFR<50ml/min的个体中,普伐他汀组的MDRD - GFR变化率比安慰剂组每年慢0.6ml/min/1.73m²(95%CI,-0.1至1.2;P = 0.07),在MDRD - GFR<40ml/min/1.73m²/年的个体中,每年慢2.5ml/min/1.73m²(95%CI,慢1.4至3.6;P = 0.0001)。与基线时无蛋白尿的参与者相比,普伐他汀在有蛋白尿的参与者中也能更大程度地降低肾功能丧失率(P = 0.006)。结论是,普伐他汀可能会减缓中度至重度肾病患者的肾功能丧失,尤其是那些有蛋白尿的患者。这些发现需要通过专门针对慢性肾功能不全患者进行的大型随机试验来证实。