Table 4.
Study | Intervention | Comparator | Duration (y) | Sample (mean eGFR±SD) | Outcome |
---|---|---|---|---|---|
NDD-CKD | |||||
SHARP59 (2011) | Simvastatin 20 mg/d + ezetimibe 10 mg/d | Placebo | 5.0 | 6,247 NDD-CKD pts (26.6±12.9 vs. 26.6±13.1); 3,023 CKD-5D pts | Primary outcome (composite of MI, coronary death, non-hemorrhagic stroke, or arterial revascularization): RR, 0.78 (0.67-0.91) in NDD-CKD |
CKD-5D | |||||
4D60 (2005) | Atorvastatin 20 mg/d | Placebo | 4.0 | 1,255 prevalent HD pts w/DM | Primary outcome (composite of CV death, MI, or stroke): RR, 0.92 (0.77-1.10) |
AURORA61 (2009) | Rosuvastatin 10 mg/d | Placebo | 5.0 | 2,776 prevalent HD pts | Primary outcome (composite of CV death, MI, or stroke): HR, 0.96 |
SHARP59 (2011) | Simvastatin 20 mg/d + ezetimibe 10mg/d | Placebo | 5.0 | 6,247 NDD-CKD pts; 3,023 CKD-5D pts (2,527 HD; 496 PD) | Primary outcome (composite of MI, coronary death, non-hemorrhagic stroke, or arterial revascularization): RRs of 0.90 (0.75-1.08) in CKD-5D, 0.95 (0.78-1.15) in HD, 0.70 (0.46-1.08) in PD |
Abbreviations: 4D, Deutsche Diabetes Dialyse Studie; AURORA, Assessment of Survival and Cardiovascular Events; CKD-5D, dialysis-dependent chronic kidney disease; CV, cardiovascular; HD, hemodialysis; MI, myocardial infarction; NDD-CKD, non-dialysis-dependent chronic kidney disease; PD, peritoneal dialysis; RR, relative risk (values in parentheses are 95% confidence intervals); SD, standard deviation; SHARP, Study of Heart and Renal Protection; HR, hazard ratio.