[Statins in patients with kidney failure: efficacy, tolerance, and prescription guidelines in patients with chronic kidney disease and renal transplant]

Presse Med. 2006 Feb;35(2 Pt 1):219-29. doi: 10.1016/s0755-4982(06)74557-2.
[Article in French]

Abstract

Background: Chronic kidney disease (CKD) is extremely common in adults, although often undiagnosed and thus untreated. Cardiovascular disease is the leading cause of death among patients with CKD and reducing its risk in this population is an important priority. Dyslipidemia is almost always present when proteinuria is above 3 gr/24 hours. Roughly two thirds of all patients with end-stage renal failure and kidney transplants suffer from dyslipidemia and should receive lipid-lowering therapy, as suggested by recent Afssaps (French drug agency) and NKF-K/DOQI (National Kidney Foundation-Kidney Disease Outcomes Quality Initiative) guidelines. We reviewed recent studies on efficacy, tolerability and prescription recommendations of statins in CKD and renal transplant patients.

Methods: We searched Medline, the international medical database, to conduct a systematic review of the literature on the efficacy and tolerability of statins in CKD and renal transplant patients and on specific recommendations for dosage adjustments in this population.

Results: The efficacy of statins in decreasing total cholesterol and LDL-cholesterol levels in dialysis and renal transplant patients is similar to that in the general population. On the other hand, large-scale randomized clinical trials among CKD (4D) and renal transplant (ALERT) patients do not demonstrate that statins significantly decrease rates of cardiovascular disease. They have a beneficial effect on proteinuria and lower the rate of kidney function deterioration in patients with dyslipidemia. Early introduction of a statin in transplant patients did not lead to improved kidney function or prevent loss of the graft. Although most statins are not excreted by the kidneys, the dosage of some must be adapted in CKD patients because of pharmacokinetic modifications induced by renal impairment.

Conclusion: Statins at appropriately adapted doses have the same efficacy in CKD patients as in subjects with normal kidney function, and tolerance is not a problem. Their effectiveness in cardiovascular prevention in this population has not been demonstrated to date. Results about statin-induced kidney protection are encouraging but further and more specific studies are needed.

Publication types

  • Comparative Study
  • Review
  • Systematic Review

MeSH terms

  • Adult
  • Aged
  • Anticholesteremic Agents / administration & dosage
  • Anticholesteremic Agents / therapeutic use*
  • Atorvastatin
  • Cardiovascular Diseases / prevention & control
  • Cholesterol / blood
  • Cholesterol, LDL / blood
  • Dyslipidemias / complications
  • Dyslipidemias / drug therapy*
  • Fatty Acids, Monounsaturated / administration & dosage
  • Fatty Acids, Monounsaturated / therapeutic use
  • Fluorobenzenes / administration & dosage
  • Fluorobenzenes / therapeutic use
  • Fluvastatin
  • Graft Rejection / prevention & control
  • Heptanoic Acids / administration & dosage
  • Heptanoic Acids / therapeutic use
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Hypolipidemic Agents / administration & dosage
  • Hypolipidemic Agents / therapeutic use
  • Indoles / administration & dosage
  • Indoles / therapeutic use
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / drug therapy*
  • Liver Transplantation*
  • Middle Aged
  • Pravastatin / administration & dosage
  • Pravastatin / therapeutic use
  • Primary Prevention
  • Prospective Studies
  • Proteinuria / drug therapy
  • Proteinuria / etiology
  • Pyrimidines / administration & dosage
  • Pyrimidines / therapeutic use
  • Pyrroles / administration & dosage
  • Pyrroles / therapeutic use
  • Randomized Controlled Trials as Topic
  • Renal Dialysis
  • Risk Factors
  • Rosuvastatin Calcium
  • Simvastatin / administration & dosage
  • Simvastatin / therapeutic use
  • Sulfonamides / administration & dosage
  • Sulfonamides / therapeutic use
  • Time Factors

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL
  • Fatty Acids, Monounsaturated
  • Fluorobenzenes
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Hypolipidemic Agents
  • Indoles
  • Pyrimidines
  • Pyrroles
  • Sulfonamides
  • Fluvastatin
  • Rosuvastatin Calcium
  • Cholesterol
  • Atorvastatin
  • Simvastatin
  • Pravastatin