Rosuvastatin to Prevent Vascular Events in Men and Women with Elevated C-Reactive Protein

Date
2008-11-20Author
Ridker, Paul M.
Danielson, Eleanor
Fonseca, Francisco A. H. [UNIFESP]
Genest, Jacques
Gotto, Antonio M.
Kastelein, John J. P.
Koenig, Wolfgang
Libby, Peter
Lorenzatti, Alberto J.
MacFadyen, Jean G.
Nordestgaard, Borge G.
Shepherd, James
Willerson, James T.
Glynn, Robert J.
JUPITER Study Grp
Type
ArtigoISSN
0028-4793Is part of
New England Journal of MedicineDOI
10.1056/NEJMoa0807646Metadata
Show full item recordAbstract
Background: Increased levels of the inflammatory biomarker high-sensitivity C-reactive protein predict cardiovascular events. Since statins lower levels of high-sensitivity C-reactive protein as well as cholesterol, we hypothesized that people with elevated high-sensitivity C-reactive protein levels but without hyperlipidemia might benefit from statin treatment.Methods: We randomly assigned 17,802 apparently healthy men and women with low-density lipoprotein (LDL) cholesterol levels of less than 130 mg per deciliter (3.4 mmol per liter) and high-sensitivity C-reactive protein levels of 2.0 mg per liter or higher to rosuvastatin, 20 mg daily, or placebo and followed them for the occurrence of the combined primary end point of myocardial infarction, stroke, arterial revascularization, hospitalization for unstable angina, or death from cardiovascular causes.Results: the trial was stopped after a median follow-up of 1.9 years (maximum, 5.0). Rosuvastatin reduced LDL cholesterol levels by 50% and high-sensitivity C-reactive protein levels by 37%. the rates of the primary end point were 0.77 and 1.36 per 100 person-years of follow-up in the rosuvastatin and placebo groups, respectively (hazard ratio for rosuvastatin, 0.56; 95% confidence interval [CI], 0.46 to 0.69; P<0.00001), with corresponding rates of 0.17 and 0.37 for myocardial infarction (hazard ratio, 0.46; 95% CI, 0.30 to 0.70; P=0.0002), 0.18 and 0.34 for stroke (hazard ratio, 0.52; 95% CI, 0.34 to 0.79; P=0.002), 0.41 and 0.77 for revascularization or unstable angina (hazard ratio, 0.53; 95% CI, 0.40 to 0.70; P<0.00001), 0.45 and 0.85 for the combined end point of myocardial infarction, stroke, or death from cardiovascular causes (hazard ratio, 0.53; 95% CI, 0.40 to 0.69; P<0.00001), and 1.00 and 1.25 for death from any cause (hazard ratio, 0.80; 95% CI, 0.67 to 0.97; P=0.02). Consistent effects were observed in all subgroups evaluated. the rosuvastatin group did not have a significant increase in myopathy or cancer but did have a higher incidence of physician-reported diabetes.Conclusions: in this trial of apparently healthy persons without hyperlipidemia but with elevated high-sensitivity C-reactive protein levels, rosuvastatin significantly reduced the incidence of major cardiovascular events. (ClinicalTrials.gov number, NCT00239681.).
Citation
New England Journal of Medicine. Waltham: Massachusetts Medical Soc, v. 359, n. 21, p. 2195-2207, 2008.Sponsorship
AstraZenecaNovartis
Merck
Abbott
Roche
Sanofi-Aventis
Merck-Schering-Plough
Isis
Dade Behring
Vascular Biogenics
Pfizer
Merck Frosst
Resverlogix
Dupont
Aegerion
Arisaph
Kowa
Genentech
Martek
Reliant
Genzyme
GlaxoSmithKline
Boehringer Ingelheim
DiaDexus
Medlogix
Anthera
Bristol-Myers Squibb
VIA Pharmaceuticals
Interleukin Genetics
Kowa Research Institute
Takeda
BG Medicine
Oxford Biosciences
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