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Cardiovascular Research 2007 73(1):237-246; doi:10.1016/j.cardiores.2006.10.021
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Copyright © 2006, European Society of Cardiology

ACE inhibition with perindopril and endothelial function. Results of a substudy of the EUROPA study: PERTINENT

Claudio Ceconia, Kim M. Foxb, William J. Remmec, Marteen L. Simoonsd, Michael Bertrande, Giovanni Parrinellof, Cornelius Kluftg, Andrew Blannh, Dennis Cokkinosi and Roberto Ferraria,*

aUniversity of Ferrara and Cardiovascular Pathophysiology Research Centre, Salvatore Maugeri Foundation, IRCCS, Gussago (Brescia), Italy
bRoyal Brompton Hospital, London, UK
cSticares, Cardiovascular Research Foundation, Rhoon, Netherlands
dErasmus University, Medical Centre Thorax Centre, Rotterdam, Netherlands
eHôpital Cardiologique Lille, France
fMedical Statistics Unit, University of Brescia, Italy
gDepartment of Vascular and Connective Tissue Research, Gaubius Laboratory TNO-PG, Leiden, Netherlands
hHaemostasis, Thrombosis and Vascular Biology Unit, University Department of Medicine, Birmingham, UK
iOnassis Cardiac Surgery Centre, Athens, Greece

* Corresponding author. Arcispedale S. Anna, University of Ferrara, Corso Giovecca 203, 44100, Ferrara, Italy. Tel.: +39 0532 202143; fax: +39 0532 241885. Email address: fri{at}dns.unife.it

Objectives: EUropean trial on Reduction Of cardiac events with Perindopril in stable coronary Artery disease [EUROPA] demonstrates reduction in cardiovascular mortality and myocardial infarction for a possible vascular and antiatherosclerotic effect of angiotensin-converting enzyme (ACE) inhibition with perindopril. Our objective was to study the effect of perindopril on endothelial function and to verify its link to risk and occurrence of cardiovascular events.

Methods: Blood from 1200 EUROPA patients was withdrawn at baseline and after 1 year of treatment with either perindopril or placebo to measure von Willebrand factor and from 45 healthy subjects and 87 EUROPA patients to study endothelial function at the cellular level by cultivating in vitro human umbilical vein endothelial cells. In this setting, we determined protein expression/activity of endothelial nitric oxide synthase and the rate of apoptosis. Plasma levels of angiotensin II, bradykinin, tumor necrosis factor {alpha}, and nitrite/nitrate were also measured.

Results: The occurrence of cardiovascular events was related to von Willebrand factor at baseline (P=0.013) that also significantly decreased after 1 year's treatment (P<0.001). Perindopril upregulated 19% and 27% protein expression/activity of endothelial nitric oxide synthase (P<0.05) as well as reduced the rate of apoptosis by 31% (P<0.05). There was also a significant reduction in levels of angiotensin II, increase in bradykinin, reduction in tumor necrosis factor {alpha}, and increase in nitrite/nitrate (P<0.05 for all).

Conclusions: Abnormal endothelial function occurs in patients with coronary artery disease, and this can be counteracted by angiotensin-converting enzyme inhibition with perindopril. These effects could contribute, at least in part, to explaining the results of the main EUROPA Study.

KEYWORDS Inhibition; Perindopril; Endothelial function; von Willebrand factor


Time for primary review 18 days


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