[临床医学]他汀的疗效与安全性.ppt

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[临床医学]他汀的疗效与安全性

Objectives We evaluated the efficacy of statin therapy in primary prevention among individuals with moderate chronic kidney disease (CKD). Background Whether patents with moderate CKD (estimated glomerular filtration rate [eGFR] 60 ml/min/1.73 m2) benefit from statin therapy is uncertain, particularly among those without hyperlipidemia or known cardiovascular disease. Methods Within the JUPITER (Justification for the Use of statins in Prevention–an Intervention Trial Evaluating Rosuvastatin) primary prevention trial of rosuvastatin 20 mg compared with placebo among men and women free of cardiovascular disease who had low-density lipoprotein cholesterol (LDL-C) 130 mg/dl and high-sensitivity C-reactive protein (hsCRP) 2 mg/l, we performed a secondary analysis comparing cardiovascular and mortality outcomes among those with moderate CKD at study entry (n 3,267) with those with baseline eGFR 60 ml/min/1.73 m2 (n 14,528). Median follow-up was 1.9 years (maximum 5 years). Results Compared with those with eGFR 60 ml/min/1.73 m2, JUPITER participants with moderate CKD had higher vascular event rates (hazard ratio [HR]: 1.54, 95% confidence interval [CI]: 1.23 to 1.92, p 0.0002). Among those with moderate CKD, rosuvastatin was associated with a 45% reduction in risk of myocardial infarction, stroke, hospital stay for unstable angina, arterial revascularization, or confirmed cardiovascular death (HR: 0.55, 95% CI: 0.38 to 0.82, p 0.002) and a 44% reduction in all-cause mortality (HR: 0.56, 95% CI: 0.37 to 0.85, p 0.005). Median LDL-C and hsCRP reductions as well as side effect profiles associated with rosuvastatin were similar among those with and without CKD. Median eGFR at 12 months was marginally improved among those allocated to rosuvastatin as compared with placebo. Conclusions Rosuvastatin reduces first cardiovascular events and all-cause mortality among men and women with LDL-C 130 mg/dl, elevated hsCRP, and concomitant evidence of moderate CKD. (JUPITER—Crestor

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