Division of Renal Diseases and Hypertension, University of Colorado Denver Health Sciences Center, Aurora, CO 80220, USA.
Am J Kidney Dis. 2010 Jan;55(1):42-9. doi: 10.1053/j.ajkd.2009.09.020. Epub 2009 Nov 22.
Chronic kidney disease (CKD) is associated with an increased risk of incident cardiovascular disease (CVD); however, the role of statins for the primary prevention of acute cardiovascular events in patients with CKD and the effect of statins on kidney function loss in persons without prevalent CVD have not been studied.
Post hoc analysis of the Air Force/Texas Coronary Atherosclerosis Prevention Study.
SETTING & PARTICIPANTS: Multicenter, randomized, double-blind, placebo-controlled trial of 5,608 men and 997 women without CVD randomly assigned to treatment with lovastatin or placebo.
Placebo or lovastatin, 20 mg/d.
OUTCOMES & MEASUREMENTS: First major acute cardiovascular event in participants with mild CKD and kidney function loss in persons with or without CKD. Estimated glomerular filtration rate was calculated using the 4-variable Modification of Diet in Renal Disease Study equation.
At baseline, mean estimated glomerular filtration rate in participants with CKD (n = 304) was 53.0 +/- 6.0 mL/min/1.73 m(2). After an average follow-up of 5.3 +/- 0.8 years, the incidence of a fatal and nonfatal CVD event was lower in participants with CKD receiving lovastatin than in those receiving placebo (adjusted relative risk [RR], 0.31; 95% CI, 0.13-0.72; P = 0.01). Tests for interaction suggested that the benefit of lovastatin was independent of the presence of CKD. Lovastatin did not reduce the annualized mean decrease in estimated glomerular filtration rate (-1.3 +/- 0.07 vs -1.4 +/- 0.07 mL/min/1.73 m(2)/y, respectively; P = 0.1) or the frequency of a > or = 25% decrease in kidney function (adjusted RR, 1.10; 95% CI, 0.96-1.28; P = 0.2) or incident CKD (adjusted RR, 1.04; 95% CI, 0.86-1.27; P = 0.6).
Unable to determine the cause and duration of kidney disease, and information regarding proteinuria was not available.
Lovastatin is effective for the primary prevention of CVD in patients with CKD, but is not effective in decreasing kidney function loss in persons with no CVD.
慢性肾病(CKD)与心血管疾病(CVD)事件的发生率增加相关;然而,他汀类药物在 CKD 患者中的急性心血管事件一级预防作用,以及他汀类药物对无 CVD 人群肾功能丧失的影响尚未得到研究。
空军/德克萨斯州冠状动脉粥样硬化预防研究的事后分析。
5608 名男性和 997 名女性无 CVD 的多中心、随机、双盲、安慰剂对照试验,随机分配接受洛伐他汀或安慰剂治疗。
安慰剂或洛伐他汀,20mg/d。
轻度 CKD 患者的首次主要急性心血管事件和 CKD 或无 CKD 患者的肾功能丧失。采用 4 变量改良肾脏病饮食研究方程计算肾小球滤过率估计值。
在基线时,CKD 患者(n=304)的平均估计肾小球滤过率为 53.0±6.0mL/min/1.73m²。在平均 5.3±0.8 年的随访后,接受洛伐他汀治疗的 CKD 患者发生致命和非致命 CVD 事件的发生率低于接受安慰剂治疗的患者(调整后的相对风险[RR],0.31;95%可信区间,0.13-0.72;P=0.01)。交互检验提示洛伐他汀的获益与 CKD 的存在无关。洛伐他汀并未降低估计肾小球滤过率的年化平均下降(-1.3±0.07 与-1.4±0.07mL/min/1.73m²/y,分别;P=0.1)或肾功能下降>或=25%的频率(调整后的 RR,1.10;95%可信区间,0.96-1.28;P=0.2)或新发 CKD(调整后的 RR,1.04;95%可信区间,0.86-1.27;P=0.6)。
无法确定肾脏疾病的病因和持续时间,也没有蛋白尿信息。
洛伐他汀可有效预防 CKD 患者的 CVD,但对无 CVD 人群肾功能丧失无效。