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Angiology
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*Angioplasty
*Peripheral Arterial Disease
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*QUINAPRIL HYDROCHLORIDE
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Article

Comparison of Selective AT1-Receptor Blockade Versus ACE Inhibition for Restenosis Prophylaxis in Patients With Peripheral Occlusive Arterial Disease After Stent Angioplasty: A Randomized, Controlled Proof-of-Concept Study

Christoph Schindler, MD1*, Axel Mueller, MD2, Peter Bramlage, MD1, Wolfgang Boecking, MD1, Wilhelm Kirch, MD, PhD1, and Johannes Schweizer, MD2

1 Medical Faculty of the Technical University of Dresden
2 Chemnitz Hospital, Germany

* To whom correspondence should be addressed. E-mail: christoph.schindler{at}tu-dresden.de.


   Abstract
Different components of the renin-angiotensin system (RAS) have been demonstrated in atherosclerotic plaques. However, the involvement of the RAS in the complex process of in-stent restenosis is not yet clear. In this prospective, randomized, double-blind, controlled proof-of-concept study, we compared the 2 different pharmacological approaches, selective AT1-receptor-blockade with candesartan vs ACE inhibition with quinapril to reduce in-stent restenosis after stent angioplasty of the superficial femoral artery. Twenty-two hypertensive patients with stage IIb peripheral occlusive arterial disease and severe claudication who had been successfully treated with percutaneous transluminal angioplasty (PTA) and stent implantation were randomly assigned to receive daily doses of either candesartan (32 mg) or quinapril (20 mg). Primary end point was restenosis 6 months after intervention, assessed by angiography. Secondary end points were pain-free walking distance, determined by treadmill ergometry; determination of crurobrachial indices; and intima-media thickness (IMT). At 6 months, the rate of restenosis on angiography was 34% in the candesartan group and 71% in the quinapril group (P = .043). Relevant restenosis was found in 3 patients (27%) in the candesartan group and in 7 patients (64%) in the quinapril group. Patients in the candesartan group were able to walk farther on a treadmill (increase: 135 m ± 20 m) compared with patients in the quinapril group (increase: 83 m ± 21 m). The IMT at the stent edge was not significantly different in the 2 groups (candesartan: 1.9 mm ± 0.5 mm; quinapril: 2.0 mm ± 0.3 mm). This study revealed significant benefit of a pharmacological restenosis regimen using the AT1-receptor antagonist candesartan in patients with severe atherosclerosis after superficial femoral artery stenting compared with treatment with the ACE inhibitor quinapril. Further prospective studies in patients are required to confirm these results.

First published on October 10, 2007, doi:10.1177/0003319707305962

Angiology 2008;58:710.

A more recent version of this article appeared on January 1, 2008


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