© 2005 by the American Diabetes Association, Inc.
Two-Year Statin Therapy Does Not Alter the Progression of Intima-Media Thickness in Patients With Type 2 Diabetes Without Manifest Cardio-vascular DiseaseResponse to Beishuizen et al.
1 "G Descovich" Atherosclerosis and Metabolic Diseases Research Center, University of Bologna, Bologna, Italy Address correspondence to Arrigo F.G. Cicero, MD, "G Descovich" Atherosclerosis and Metabolic Diseases Research Center, University of Bologna, Via Massarenti, 9, 40138, Bologna, Italy. E-mail: afgcicero{at}cardionet.it We read the recent study by Beishuizen et al. (1), which claims that statin treatment had no effect on intima-media thickness (IMT) in diabetic subjects. We agree that contrary to the suggestions made in the Third Report of the Adult Treatment Panel of the National Cholesterol Education Program (2), diabetes is not always a cardiovascular disease equivalent in terms of cardiovascular event risk and that this risk is more related to the individual level of other cardiovascular risk factors. However, it is hard to conclude that statins are ineffective in reducing IMT in diabetics subjects on the basis of the reported data because of some relevant methodological problems. The main problem is the change in statins tested during the study. In fact, until now, no trial has demonstrated that statin switch is as efficacious as continuous treatment with a single statin on vascular protection. Then, the LDL cholesterollowering effect of 0.4 mg cerivastatin is not equal to that of 20 mg simvastatin. The authors admit that mean LDL cholesterolemia significantly increased after statin switch. At the end of the study, the placebo group was smaller than estimated to be sufficient to detect significant differences between groups. Some randomization problems are also foreseeable by the 87% relative risk reduction in cardiovascular disease rates and by the 100% relative risk reduction in coronary artery disease rates in statin-treated patients after only 24 months of treatment, which is much higher than that observed in the diabetic group of the HPS (Heart Protection Study) (3) or in CARDS (Collaborative Atorvastatin Diabetes Study) (4) (or in any other large statin clinical trial). Moreover, it is not correct to compare the observed results with those obtained with bezafibrate, which is not an antihypercholesterolemic drug and has a completely different pharmacodynamic profile. In our opinion, on the basis of the reported data, Beishuizen et al. should have concluded that 15.4 months of treatment with 0.4 mg cerivastatin (not generically "statins") is not efficacious in reducing IMT progression in type 2 diabetic subjects. Footnotes A.F.G.C. has received honoraria from Sankyo Pharma and Bayer. A.V.G. has received honoraria from Sankyo Pharma, Bayer, MSD, Novartis, Pfizer, Fournier Pharma, and Chiesi Farmaceutici and has received research support from MSD, Novartis, and Astra Zeneca. G.D. has received honoraria from Guidotti, Menarini, Aventis, Roche, MSD, Merck SA, and Fournier Pharma. References
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