Copyright
©The Author(s) 2015.
World J Nephrol. Feb 6, 2015; 4(1): 83-91
Published online Feb 6, 2015. doi: 10.5527/wjn.v4.i1.83
Published online Feb 6, 2015. doi: 10.5527/wjn.v4.i1.83
Trial | Study population | Intervention | Follow-up | Major findings |
ALERT (2003) | Renal transplant recipients (n = 2102) | Fluvastatin (40 mg/d) vs placebo | Mean 5.1 yr | Fluvastatin group had reduced major cardiac events and cardiac death but this was not statistically significant No effect seen on all-cause mortality |
4D (2005) | Hemodialysis patients with DM type II (n = 1255) | Atorvastatin (20 mg/d) | Median 4 yr | Atorvastatin did not have significant effect on CV death, non-fatal MI, non-fatal stroke and all-cause mortality |
AURORA (2009) | Hemodialysis patients aged 50-80 yr (n = 2776) | Rosuvastatin (10 mg/d) vs placebo | Median 3.8 yr | Rosuvastatin had no significant effect on CV mortality, non-fatal MI, non-fatal stroke and all-cause mortality |
SHARP (2011) | CKD not on dialysis (n = 6247) Hemodialysis (n = 2527) Peritoneal dialysis (n = 496) | Simvastatin 20 mg/d plus ezetimibe 10 mg/d vs placebo | Median 4.9 yr | Simvastatin plus ezetimibe significantly decreased major atherosclerotic event but had no major effect on CV mortality or all-cause mortality. Results were available for only entire population (both dialysis and non-dialysis) |
- Citation: Pandya V, Rao A, Chaudhary K. Lipid abnormalities in kidney disease and management strategies. World J Nephrol 2015; 4(1): 83-91
- URL: https://www.wjgnet.com/2220-6124/full/v4/i1/83.htm
- DOI: https://dx.doi.org/10.5527/wjn.v4.i1.83