Aims We sought to examine the interrelationship between statin use, inflammation, and outcome of high-risk patients with advanced atherosclerosis. Methods and results We prospectively studied 515 patients with severe peripheral artery disease (median age 70 years, 296 mates). The cardiovascular risk profile and laboratory parameters of inflammation (high -sensitivity C-reactive protein [hs-CRP],serum amyloid A [SAA], fibrinogen, serum albumin, neutrophil counts) were obtained, and patients were followed for a median of 21 months (interquartile range 12-25) for the occurrence of myocardial infarction (MI) and death. We observed 19 Mls (5 fatal and 14 nonfatal) and 65 deaths. Cumulative survival and event-free survival rates (freedom from death and MI) at 6, 12, and 24 months were 97%, 95%, and 89%, and 96%, 93% and 87%, respectively. Patients receiving statin therapy (n = 269, 52%) had a tower level of inflammation (hs-CRP p < 0.001, SAA p = 0.001, fibrinogen p = 0.007, albumin p < 0.001, neutrophils p = 0.049) and better survival (adjusted hazard ratio [HR] 0.52, p = 0.022) and event-free survival rates (adjusted HR 0.48, p = 0.004) than patients not treated with statins. However, patients with tow inflammatory activity (hs-CRP less than or equal to0.42 mg/dl) had no significant benefit from statin therapy (p = 0.74 for survival; p = 0.83 for event-free survival), whereas in patients with high hs-CRP (>0.42 mg/dl) statin therapy was associated with a significantly reduced risk for mortality (adjusted HR 0.58, p = 0.046) and the composite of myocardial infarction and death (adjusted HR 0.46, p = 0.016). Conclusion Statin therapy is associated with a substantially improved intermediate-term survival of patients with severe peripheral artery disease and a high inflammatory activity, whereas in patients with low hs-CRP no survival benefit was observed. (C) 2004 The European Society of Cardiology. Published by Elsevier Ltd. All rights reserved.