首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Effects of atorvastatin on kidney outcomes and cardiovascular disease in patients with diabetes: an analysis from the Collaborative Atorvastatin Diabetes Study (CARDS).
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Effects of atorvastatin on kidney outcomes and cardiovascular disease in patients with diabetes: an analysis from the Collaborative Atorvastatin Diabetes Study (CARDS).

机译:阿托伐他汀对糖尿病患者肾脏结局和心血管疾病的影响:阿托伐他汀糖尿病合作研究的分析。

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BACKGROUND: We examined whether atorvastatin affects diabetic kidney disease and whether the effect of atorvastatin on cardiovascular disease (CVD) varies by kidney status in patients with diabetes. STUDY DESIGN: The Collaborative Atorvastatin Diabetes Study (CARDS) randomized placebo-controlled trial. SETTING & PARTICIPANTS: Patients with type 2 diabetes and no prior CVD (n = 2,838). INTERVENTION: Random allocation to atorvastatin, 10 mg/d, or placebo, with a median follow-up of 3.9 years. OUTCOMES: Estimated glomerular filtration rate (eGFR), albuminuria, CVD. MEASUREMENTS: Baseline and follow-up GFRs were estimated by using the Modification of Diet in Renal Disease Study equation. Urinary albumin-creatinine ratio was measured on spot urine samples. RESULTS: At baseline, 34% of patients had an eGFR of 30 to 60 mL/min/1.73 m(2). Atorvastatin treatment was associated with a modest improvement in annual change in eGFR (net, 0.18 mL/min/1.73 m(2)/y; 95% confidence interval [CI], 0.04 to 0.32; P = 0.01) that was most apparent in those with albuminuria (net improvement, 0.38 mL/min/1.73 m(2)/y; P = 0.03). At baseline, 21.5% of patients had albuminuria and an additional 6.8% developed albuminuria during follow-up. Atorvastatin did not influence the incidence of albuminuria (hazard ratio, 1.49; 95% CI, 0.73 to 3.04; P = 0.3) or regression to normoalbuminuria (hazard ratio, 1.19; 95% CI, 0.57 to 2.49; P = 0.6). In 970 patients with a moderately decreased eGFR of 30 to 60 mL/min/1.73 m(2), there was a 42% reduction in major CVD events with treatment, including a 61% reduction in stroke. This treatment effect was similar to the 37% (95% CI, 17 to 52; P < 0.001) reduction in CVD observed in the study overall (P = 0.4 for the eGFR-treatment interaction). LIMITATIONS: Low incidence rates of albuminuria and transition to more severe kidney status limit power to detect treatment effects. CONCLUSIONS: A modest beneficial effect of atorvastatin on eGFR, particularly in those with albuminuria, was observed. Atorvastatin did not influence albuminuria incidence. Atorvastatin was effective at decreasing CVD in those with and without a moderately decreased eGFR and achieved a high absolute benefit.
机译:背景:我们研究了阿托伐他汀是否会影响糖尿病肾病,以及阿托伐他汀对心血管疾病(CVD)的影响是否因糖尿病患者的肾脏状况而异。研究设计:阿托伐他汀糖尿病合作研究(CARDS)随机安慰剂对照试验。地点和参与者:2型糖尿病患者,既往无CVD(n = 2,838)。干预:随机分配给阿托伐他汀10 mg / d或安慰剂,平均随访3.9年。结果:估计的肾小球滤过率(eGFR),蛋白尿,CVD。测量:通过使用饮食中肾脏疾病研究方程的修正来估计基线和随访GFR。测定尿样中尿白蛋白-肌酐的比例。结果:在基线时,34%的患者的eGFR为30至60 mL / min / 1.73 m(2)。阿托伐他汀治疗与eGFR年度变化的适度改善有关(净值,0.18 mL / min / 1.73 m(2)/ y; 95%置信区间[CI],0.04至0.32; P = 0.01),在患有蛋白尿的患者(净改善0.38 mL / min / 1.73 m(2)/ y; P = 0.03)。在基线时,随访期间有21.5%的患者患有蛋白尿,另有6.8%的患者发展为蛋白尿。阿托伐他汀不影响蛋白尿的发生率(危险比1.49; 95%CI为0.73至3.04; P = 0.3)或回归至白蛋白尿(危险比为1.19; 95%CI为0.57至2.49; P = 0.6)。在970名患者的eGFR适度降低的患者中,eGFR降低了30至60 mL / min / 1.73 m(2),治疗中的主要CVD事件减少了42%,包括卒中减少了61%。该治疗效果类似于研究总体观察到的CVD降低37%(95%CI,17至52; P <0.001)(eGFR与治疗的相互作用P = 0.4)。局限性:蛋白尿的低发生率和向更严重肾脏状态的转变限制了检测治疗效果的能力。结论:阿托伐他汀对eGFR有中等程度的有益作用,特别是在患有蛋白尿的患者中。阿托伐他汀不影响白蛋白尿的发生率。阿托伐他汀在有或没有eGFR适度降低的患者中均有效降低CVD,并获得了很高的绝对收益。

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