Thromb Haemost 2008; 99(01): 182-189
DOI: 10.1160/TH07-04-0265
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

High-dose atorvastatin in peripheral arterial disease (PAD): Effect on endothelial function, intima-media-thickness and local progression of PAD

An open randomized controlled pilot trial
Silviana Spring
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Roger Simon
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Bernd van der Loo
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Tamara Kovacevic
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Christiane Brockes
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Valentin Rousson
2   Department of Biostatistics, ISPM, University Zurich, Zurich, Switzerland
,
Beatrice Amann-Vesti
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
,
Renate Koppensteiner
1   Clinic of Angiology, Department of Medicine, University Hospital Zurich, Switzerland
› Author Affiliations

Financial support: The study was an investigator-initiated trial and was supported by a research grant from Pfizer AG.
Further Information

Publication History

Received: 12 April 2007

Accepted after major revision: 02 November 2007

Publication Date:
24 November 2017 (online)

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Summary

Beneficial effects of aggressive lipid-lowering with high-dose atorvastatin (80 mg/day) have been demonstrated in patients with coronary and cerebrovascular disease. The impact of such a therapy in patients with peripheral arterial disease (PAD) is less known so far. Here we studied the effects of high-dose atorvastatin on brachial artery endothelial function, common carotid intima-media thickness (IMT) and local progression of PAD in these patients. One hundred of 500 patients screened with documented PAD were randomly assigned to receive 80 mg of atorvastatin daily for six months or to continue on conventional medical treatment. Ninety-six percent of patients in the control group were on standard statin treatment. High resolution B-mode ultrasonography was used to study brachial artery flowmediated dilation (FMD), IMT and ankle-brachial index (ABI) at baseline and at six months. FMD and IMT at baseline and at six months were 4.1 (0.06–8.6) versus 5.0 (0.76 vs. 8.1) %, p=0.96, and 0.76 (0.66–0.82) versus 0.73 (0.63–0.81) mm, p=0.41, respectively, in the atorvastatin group, and 2.66 (-1.9 – 6.9) versus 3.65 (0.0–8.6)%, p=0.02, and 0.78 (0.71–0.90) versus 0.77 (0.70–0.90) mm, p=0.48,in the control group. ABI at baseline and at six months was not different in either group. LDL cholesterol was reduced from 2.53 (2.21–3.28) to 1.86 (1.38–2.29) mM (p<0.0001) in the atorvastatin group, whereas levels remained stable in the control group [2.38 (1.94–3.16) vs.2.33 (1.82–2.84) mM, p=0.61]. Major adverse cardiovascular events occurred in 2.1% in the atorvastatin group and 1.9% in the control group (p= 0.61). In conclusion, in this pilot trial aggressive lipid-lowering with 80 mg of atorvastatin daily for six months had no effect on brachial artery FMD in patients with PAD. IMT andABI were also similar in patients with and without high-dose atorvastatin at six months.