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Rosuvastatin in hemodialysis: short-term effects on lipids and C-reactive protein
Jayme E Burmeister1, Diego R Miltersteiner, Bruno M Campos
1Renal Medicine Unit, Medicine School, Universidade Luterana do Brasil (ULBRA), Canoas, Rio Grande do Sul, Brazil. burmeister@via-rs.net
Insights
Rosuvastatin therapy effectively reduced cholesterol and C-reactive protein in hemodialysis patients. This study demonstrates rosuvastatin
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Patients undergoing regular hemodialysis exhibit elevated cardiovascular mortality.
- Uremic dyslipidemia and inflammation contribute to atherosclerosis in this population.
- The efficacy of rosuvastatin in dialysis patients remained uninvestigated.
Purpose of the Study:
- To assess the impact of rosuvastatin therapy on lipid profiles, lipoproteins, and inflammation markers in hemodialysis patients.
- To evaluate rosuvastatin's effectiveness in managing dyslipidemia and inflammation in end-stage renal disease.
Main Methods:
- A 3-month, double-blind, randomized, placebo-controlled trial involving 59 hemodialysis patients.
- Participants were assigned to receive either rosuvastatin 10 mg/day (n=28) or a placebo (n=31).
- Measurements of lipids, lipoproteins, and high-sensitivity C-reactive protein (hs-CRP) were conducted at baseline, 30 days, and 3 months.
Main Results:
- The rosuvastatin group showed significant reductions in total cholesterol, LDL cholesterol, and non-HDL cholesterol compared to baseline (p<0.05).
- No significant lipid changes were observed in the placebo group.
- High-sensitivity CRP levels were significantly lower in the rosuvastatin group versus placebo at 3 months (p<0.01).
Conclusions:
- Rosuvastatin calcium, at a dosage of 10 mg/day, demonstrated efficacy in improving lipid profiles for hemodialysis patients.
- The therapy also effectively reduced high-sensitivity C-reactive protein levels, indicating an anti-inflammatory effect.
- These findings suggest rosuvastatin is a viable option for managing cardiovascular risk factors in this patient cohort.
Background:
Patients on regular hemodialysis present high cardiovascular mortality. Uremic dyslipidemia and inflammation take part in the etiology of atherosclerosis. Rosuvastatin calcium has not been studied in patients on dialysis to date. We sought to evaluate the results of rosuvastatin therapy regarding lipids, lipoproteins and a marker of inflammation in hemodialysis patients.
Methods:
In a double-blind randomized placebo-controlled trial, 59 patients on hemodialysis (31 in the placebo group, and 28 taking rosuvastatin 10 mg/day) were followed for 3 months. Lipids, lipoproteins and high-sensitivity C-reactive protein (hs-CRP) were measured at baseline, 30 days and 3 months.
Results:
In the rosuvastatin group, there was a significant decrease from baseline to the study end in total cholesterol (163+/-53 mg/dL to 142+/-43 mg/dL; p<0.05), in LDL cholesterol (90+/-39 mg/dL to 69+/-32 mg/dL; p<0.05) and in non-HDL cholesterol (121+/-46 mg/dL to 99+/-39 mg/dL; p<0.05). In the placebo group, no significant decrease was observed. High-sensitivity CRP was lower in the rosuvastatin than in the placebo group at 3 months (p<0.01).
Conclusions:
Rosuvastatin calcium at 10 mg/day was effective in lowering total cholesterol, LDL cholesterol, non-HDL cholesterol and hs-CRP in hemodialysis patients.
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