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

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 compa...

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Veröffentlicht in:Angiology 2008-01, Vol.58 (6), p.710-716
Hauptverfasser: Schindler, Christoph, Mueller, Axel, Bramlage, Peter, Boecking, Wolfgang, Kirch, Wilhelm, Schweizer, Johannes
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container_end_page 716
container_issue 6
container_start_page 710
container_title Angiology
container_volume 58
creator Schindler, Christoph
Mueller, Axel
Bramlage, Peter
Boecking, Wolfgang
Kirch, Wilhelm
Schweizer, Johannes
description 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.
doi_str_mv 10.1177/0003319707305962
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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.</description><identifier>ISSN: 0003-3197</identifier><identifier>EISSN: 1940-1574</identifier><identifier>DOI: 10.1177/0003319707305962</identifier><identifier>PMID: 17928625</identifier><identifier>CODEN: ANGIAB</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Aged ; Angioplasty, Balloon - adverse effects ; Angioplasty, Balloon - instrumentation ; Angiotensin II Type 1 Receptor Blockers - adverse effects ; Angiotensin II Type 1 Receptor Blockers - therapeutic use ; Angiotensin-Converting Enzyme Inhibitors - adverse effects ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Ankle - blood supply ; Arterial Occlusive Diseases - complications ; Arterial Occlusive Diseases - drug therapy ; Arterial Occlusive Diseases - physiopathology ; Arterial Occlusive Diseases - therapy ; Benzimidazoles - adverse effects ; Benzimidazoles - therapeutic use ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Pressure ; Brachial Artery - physiopathology ; Cardiology. Vascular system ; Cardiovascular system ; Diseases of the cardiovascular system ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Double-Blind Method ; Female ; Femoral Artery - diagnostic imaging ; Femoral Artery - physiopathology ; Humans ; Intermittent Claudication - drug therapy ; Intermittent Claudication - etiology ; Intermittent Claudication - therapy ; Male ; Medical sciences ; Middle Aged ; Peripheral Vascular Diseases - complications ; Peripheral Vascular Diseases - drug therapy ; Peripheral Vascular Diseases - physiopathology ; Peripheral Vascular Diseases - therapy ; Pharmacology. Drug treatments ; Prospective Studies ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Recovery of Function ; Secondary Prevention ; Severity of Illness Index ; Stents ; Tetrahydroisoquinolines - adverse effects ; Tetrahydroisoquinolines - therapeutic use ; Tetrazoles - adverse effects ; Tetrazoles - therapeutic use ; Time Factors ; Treatment Outcome ; Ultrasonography ; Vasodilator agents. 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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.</description><subject>Aged</subject><subject>Angioplasty, Balloon - adverse effects</subject><subject>Angioplasty, Balloon - instrumentation</subject><subject>Angiotensin II Type 1 Receptor Blockers - adverse effects</subject><subject>Angiotensin II Type 1 Receptor Blockers - therapeutic use</subject><subject>Angiotensin-Converting Enzyme Inhibitors - adverse effects</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Ankle - blood supply</subject><subject>Arterial Occlusive Diseases - complications</subject><subject>Arterial Occlusive Diseases - drug therapy</subject><subject>Arterial Occlusive Diseases - physiopathology</subject><subject>Arterial Occlusive Diseases - therapy</subject><subject>Benzimidazoles - adverse effects</subject><subject>Benzimidazoles - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure</subject><subject>Brachial Artery - physiopathology</subject><subject>Cardiology. 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Drug treatments</subject><subject>Prospective Studies</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Recovery of Function</subject><subject>Secondary Prevention</subject><subject>Severity of Illness Index</subject><subject>Stents</subject><subject>Tetrahydroisoquinolines - adverse effects</subject><subject>Tetrahydroisoquinolines - therapeutic use</subject><subject>Tetrazoles - adverse effects</subject><subject>Tetrazoles - therapeutic use</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Ultrasonography</subject><subject>Vasodilator agents. Cerebral vasodilators</subject><subject>Walking</subject><issn>0003-3197</issn><issn>1940-1574</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi1ERZfCnRPyhRspdhLHMbcQCq1UqattgWPkdeyui9eObAex_Fn-Sie0CAnJkmfeeeZDMwi9ouSUUs7fEUKqigpOeEWYaMonaEVFTQrKeP0UrZZwscSP0fOU7sBllDTP0DHlomybkq3Q7z7sJxltCh4Hg6-10yrbHxp3N7TYaKWnHCL-4IL6LkeNv-qY5oS7_gxf-J3d2mwh0QCy0SlrH5JNeB3DtDs4-RNs6_FaZqt9TvibzTu81tFOOx2lw1dKuTn9aRYzyCB9tEnLBIIBAV9DxYw7f2vD5GTKh_e4wxvpx7C3v_T4FvfB5xicW2zoGkwBD8RlbMiex8MLdGSkS_rl43-Cvnw6u-nPi8urzxd9d1lMVJS5YE3NSUtbRWWjtlKPnFdUGd4yagwRsixNzRjITNR6FKQcKWy84sA2bdVW1Ql6_VB3mrd7PQ5TtHsZD8PfTQPw5hGQSUlnovTKpn-cEKyuWw5c8cAleauHuzBHD3MPlAzLxYf_L17dA7uHniQ</recordid><startdate>200801</startdate><enddate>200801</enddate><creator>Schindler, Christoph</creator><creator>Mueller, Axel</creator><creator>Bramlage, Peter</creator><creator>Boecking, Wolfgang</creator><creator>Kirch, Wilhelm</creator><creator>Schweizer, Johannes</creator><general>SAGE Publications</general><general>Westminster</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200801</creationdate><title>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</title><author>Schindler, Christoph ; Mueller, Axel ; Bramlage, Peter ; Boecking, Wolfgang ; Kirch, Wilhelm ; Schweizer, Johannes</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p192t-56470818c1a6cbaed7731cf7851ff09a22f455ed7594ed902d130537cba683833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Angioplasty, Balloon - adverse effects</topic><topic>Angioplasty, Balloon - instrumentation</topic><topic>Angiotensin II Type 1 Receptor Blockers - adverse effects</topic><topic>Angiotensin II Type 1 Receptor Blockers - therapeutic use</topic><topic>Angiotensin-Converting Enzyme Inhibitors - adverse effects</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Ankle - blood supply</topic><topic>Arterial Occlusive Diseases - complications</topic><topic>Arterial Occlusive Diseases - drug therapy</topic><topic>Arterial Occlusive Diseases - physiopathology</topic><topic>Arterial Occlusive Diseases - therapy</topic><topic>Benzimidazoles - adverse effects</topic><topic>Benzimidazoles - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Pressure</topic><topic>Brachial Artery - physiopathology</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular system</topic><topic>Diseases of the cardiovascular system</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Femoral Artery - diagnostic imaging</topic><topic>Femoral Artery - physiopathology</topic><topic>Humans</topic><topic>Intermittent Claudication - drug therapy</topic><topic>Intermittent Claudication - etiology</topic><topic>Intermittent Claudication - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Peripheral Vascular Diseases - complications</topic><topic>Peripheral Vascular Diseases - drug therapy</topic><topic>Peripheral Vascular Diseases - physiopathology</topic><topic>Peripheral Vascular Diseases - therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Recovery of Function</topic><topic>Secondary Prevention</topic><topic>Severity of Illness Index</topic><topic>Stents</topic><topic>Tetrahydroisoquinolines - adverse effects</topic><topic>Tetrahydroisoquinolines - therapeutic use</topic><topic>Tetrazoles - adverse effects</topic><topic>Tetrazoles - therapeutic use</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Ultrasonography</topic><topic>Vasodilator agents. 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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. 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ispartof Angiology, 2008-01, Vol.58 (6), p.710-716
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subjects Aged
Angioplasty, Balloon - adverse effects
Angioplasty, Balloon - instrumentation
Angiotensin II Type 1 Receptor Blockers - adverse effects
Angiotensin II Type 1 Receptor Blockers - therapeutic use
Angiotensin-Converting Enzyme Inhibitors - adverse effects
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Ankle - blood supply
Arterial Occlusive Diseases - complications
Arterial Occlusive Diseases - drug therapy
Arterial Occlusive Diseases - physiopathology
Arterial Occlusive Diseases - therapy
Benzimidazoles - adverse effects
Benzimidazoles - therapeutic use
Biological and medical sciences
Blood and lymphatic vessels
Blood Pressure
Brachial Artery - physiopathology
Cardiology. Vascular system
Cardiovascular system
Diseases of the cardiovascular system
Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
Double-Blind Method
Female
Femoral Artery - diagnostic imaging
Femoral Artery - physiopathology
Humans
Intermittent Claudication - drug therapy
Intermittent Claudication - etiology
Intermittent Claudication - therapy
Male
Medical sciences
Middle Aged
Peripheral Vascular Diseases - complications
Peripheral Vascular Diseases - drug therapy
Peripheral Vascular Diseases - physiopathology
Peripheral Vascular Diseases - therapy
Pharmacology. Drug treatments
Prospective Studies
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Recovery of Function
Secondary Prevention
Severity of Illness Index
Stents
Tetrahydroisoquinolines - adverse effects
Tetrahydroisoquinolines - therapeutic use
Tetrazoles - adverse effects
Tetrazoles - therapeutic use
Time Factors
Treatment Outcome
Ultrasonography
Vasodilator agents. Cerebral vasodilators
Walking
title 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
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