PMID- 11158861 OWN - NLM STAT- MEDLINE DCOM- 20010426 LR - 20190815 IS - 1523-6838 (Electronic) IS - 0272-6386 (Linking) VI - 37 IP - 1 Suppl 2 DP - 2001 Jan TI - The CHORUS (Cerivastatin in Heart Outcomes in Renal Disease: Understanding Survival) protocol: a double-blind, placebo-controlled trial in patients with esrd. PG - S48-53 AB - The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor (statin)-mediated lowering of serum cholesterol has been associated with a significant reduction in cardiovascular morbidity and mortality. Recent studies suggest that additional non-lipid lowering effects (eg, endothelial stabilization, anti-inflammatory, antithrombogenic) may be important in modulating their effectiveness. Dyslipidemia is common in end-stage renal disease (ESRD), and hemodialysis patients have increased cardiovascular morbidity and mortality. Cerivastatin, a new statin with powerful low-density lipoprotein-cholesterol (LDL-C) lowering capabilities, possesses some unique non-LDL-C-mediated properties that may contribute to a reduction of coronary events in the patient with ESRD. The primary objective of this multicenter multinational study of 1,054 hemodialysis patients is to compare 2 years of treatment with cerivastatin (0.4 mg/d) versus placebo on the composite clinical event rate of myocardial infarction, sudden cardiac death, ischemic stroke, and the need for coronary arterial bypass graft (CABG) or percutaneous transluminal coronary angioplasty (PTCA) procedures in these patients. Changes in lipids, inflammatory proteins including heat stable C-reactive protein (hsCRP), interleukin-6 (IL-6), oncostatin-M, intracellular adhesion molecule-1 (ICAM-1) and monocyte-chemoattractant protein-1 (MCP-1), as well as markers of cardiac muscle pathology, such as troponin I and troponin T, will be assessed in a subset of patients. This study is the first of its kind to assess the effect of a statin on the reduction of cardiovascular morbidity and mortality in an incident hemodialysis population. It will determine whether treatment with cerivastatin can effectively reduce the significant cardiovascular morbidity and mortality. FAU - Keane, W F AU - Keane WF AD - Department of Medicine, Hennepin County Medical Center, University of Minnesota Medical School, Minneapolis, MN, USA. g.macgregor@sghms.ac.uk FAU - Brenner, B M AU - Brenner BM FAU - Mazzu, A AU - Mazzu A FAU - Agro, A AU - Agro A LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PL - United States TA - Am J Kidney Dis JT - American journal of kidney diseases : the official journal of the National Kidney Foundation JID - 8110075 RN - 0 (Hydroxymethylglutaryl-CoA Reductase Inhibitors) RN - 0 (Pyridines) RN - AM91H2KS67 (cerivastatin) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Area Under Curve MH - Double-Blind Method MH - Female MH - Follow-Up Studies MH - Heart/drug effects/physiopathology MH - Humans MH - Hydroxymethylglutaryl-CoA Reductase Inhibitors/*therapeutic use MH - Kidney Failure, Chronic/*drug therapy/metabolism/therapy MH - Male MH - Middle Aged MH - Multicenter Studies as Topic MH - Pyridines/pharmacokinetics/*therapeutic use MH - Randomized Controlled Trials as Topic MH - Renal Dialysis MH - Research Design MH - Survival Analysis EDAT- 2001/02/13 11:00 MHDA- 2001/05/11 10:01 CRDT- 2001/02/13 11:00 PHST- 2001/02/13 11:00 [pubmed] PHST- 2001/05/11 10:01 [medline] PHST- 2001/02/13 11:00 [entrez] AID - S0272-6386(01)84851-4 [pii] AID - 10.1053/ajkd.2001.20739 [doi] PST - ppublish SO - Am J Kidney Dis. 2001 Jan;37(1 Suppl 2):S48-53. doi: 10.1053/ajkd.2001.20739.