Effect of fluvastatin on cardiac outcomes in renal transplant recipients: a multicentre, randomised, placebo-controlled trial

H Holdaas, B Fellström, AG Jardine, I Holme, G Nyberg… - The Lancet, 2003 - thelancet.com
H Holdaas, B Fellström, AG Jardine, I Holme, G Nyberg, P Fauchald, C Grönhagen-Riska…
The Lancet, 2003thelancet.com
Background Renal transplant recipients are at increased risk of premature cardiovascular
disease. Although statins reduce cardiovascular risk in the general population, their efficacy
and safety in renal transplant recipients have not been established. We investigated the
effects of fluvastatin on cardiac and renal endpoints in this population. Methods We did a
multicentre, randomised, double-blind, placebo-controlled trial in 2102 renal transplant
recipients with total cholesterol 4· 0–9· 0 mmol/L. We randomly assigned patients fluvastatin …
Background
Renal transplant recipients are at increased risk of premature cardiovascular disease. Although statins reduce cardiovascular risk in the general population, their efficacy and safety in renal transplant recipients have not been established. We investigated the effects of fluvastatin on cardiac and renal endpoints in this population.
Methods
We did a multicentre, randomised, double-blind, placebo-controlled trial in 2102 renal transplant recipients with total cholesterol 4·0–9·0 mmol/L. We randomly assigned patients fluvastatin (n=1050) or placebo (n=1052) and follow up was for 5–6 years. The primary endpoint was the occurrence of a major adverse cardiac event, defined as cardiac death, non-fatal myocardial infarction (MI), or coronary intervention procedure. Secondary endpoints were individual cardiac events, combined cardiac death or non-fatal MI, cerebrovascular events, non-cardiovascular death, all-cause mortality, and graft loss or doubling of serum creatinine. Analysis was by intention to treat.
Findings
After a mean follow-up of 5·1 years, fluvastatin lowered LDL cholesterol concentrations by 32%. Risk reduction with fluvastatin for the primary endpoint (risk ratio 0·83 [95% Cl 0·64-1·06], p=0·139) was not significant, although there were fewer cardiac deaths or non-fatal Ml (70 vs 104, 0·65 [0·48–0·88] p=0·005) in the fluvastatin group than in the placebo group. Coronary intervention procedures and other secondary endpoints did not differ significantly between groups.
Interpretation
Although cardiac deaths and non-fatal Ml seemed to be reduced, fluvastatin did not generally reduce rates of coronary intervention procedures or mortality. Overall effects of fluvastatin were similar to those of statins in other populations.
Published online June 3, 2003 http://image.thelancet.com/extras/03art4377web.pdf
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