ACE Inhibition and Endothelial Function: Main Findings of PERFECT, a Sub-Study of the EUROPA Trial
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- Cite this article as:
- Bots, M.L., Remme, W.J., Lüscher, T.F. et al. Cardiovasc Drugs Ther (2007) 21: 269. doi:10.1007/s10557-007-6041-3
ACE inhibition results in secondary prevention of coronary artery disease (CAD) through different mechanisms including improvement of endothelial dysfunction. The Perindopril-Function of the Endothelium in Coronary artery disease Trial (PERFECT) evaluated whether long-term administration of perindopril improves endothelial dysfunction.
PERFECT is a 3-year double blind randomised placebo controlled trial to determine the effect of perindopril 8 mg once daily on brachial artery endothelial function in patients with stable CAD without clinical heart failure. Endothelial function in response to ischaemia was assessed using ultrasound. Primary endpoint was difference in flow-mediated vasodilatation (FMD) assessed at 36 months.
In 20 centers, 333 patients randomly received perindopril or matching placebo. Ischemia-induced FMD was 2.7% (SD 2.6). In the perindopril group FMD went from 2.6% at baseline to 3.3% at 36 months and in the placebo group from 2.8 to 3.0%. Change in FMD after 36 month treatment was 0.55% (95% confidence interval −0.36, 1.47; p = 0.23) higher in perindopril than in placebo group. The rate of change in FMD per 6 months was 0.14% (SE 0.05, p = 0.02) in perindopril and 0.02% (SE 0.05, p = 0.74) in placebo group (0.12% difference in rate of change p = 0.07).
Perindopril resulted in a modest, albeit not statistically significant, improvement in FMD.
Key wordsACE inhibitionbrachial reactivityendothelial functioncardiovascular disease preventionatherosclerosiscoronary heart disease
ACE inhibition has been shown to reduce morbidity and mortality among a variety of patients, i.e. patients with congestive heart failure,[1–3], survivors of a myocardial infarction [4, 5], a-symptomatic patients with left ventricular dysfunction [6, 7], patients with acute myocardial infarction [8–11], post-myocardial infarction patients [6, 7, 12–14] and older high risk patients with documented coronary heart disease without heart failure and, in some, no left ventricular dysfunction . Recently, the EUROPA trial expanded the evidence by showing that ACE inhibition reduces cardiovascular event risk by 20% among a relatively low risk population of patients with stable coronary heart disease without apparent heart failure . In contrast, the PEACE trial study did not show a benefit of ACE inhibition over placebo .
Several mechanisms may explain the beneficial effects of ACE inhibition on morbidity and mortality . One of them is the effect of ACE inhibition on shifting the balance between vasoconstrictive forces (angiotensin II) and vasodilatative forces (bradykinin and nitric oxide) towards vasodilatation . Also, ACE inhibition may protect against endothelial apoptosis. These mechanisms lead to an improvement in endothelial dysfunction. The PERFECT study, as a sub-study to the EUROPA trial, was designed to verify the above mentioned pathophysiologic concept . In the PERFECT study, B-mode ultrasonography of the brachial artery was be used to assess endothelial function in response to ischaemia (reactive hyperaemia) as measured by flow mediated vasodilatation (FMD).
The present paper describes the main findings of the PERFECT study.
The rationale and design of the PERFECT study has been detailed elsewhere . In short, the PERFECT study is a study nested within the EUROPA trial. The EUROPA trial is a three year double-blind, multi-centre, placebo-controlled randomised study that aims at studying the effect of the ACE-inhibitor perindopril on morbidity and mortality in over 12,000 patients with stable coronary artery disease without clinical heart failure . The PERFECT study was designed as a parallel group randomised placebo controlled trial to determine the effect of perindopril (8 mg/day) on brachial artery endothelial function, as assessed by FMD.
After a run-in period of 4 weeks with 4 mg/day perindopril, participants were randomised to perindopril or placebo. The recruitment for the PERFECT study started in May 1998. Both the EUROPA trial and the PERFECT study finished recruitment in June 1999. In the PERFECT study 333 patients were recruited in 20 European centers (8 in Czech Republic, 1 in Germany, 2 in Greece, 4 in Netherlands, 4 in Poland and 1 in Sweden). Endothelial function, measured as FMD was assessed at the baseline visit, just before the run-in period. Follow-up B mode ultrasound for FMD assessment were performed at 6, 12, 24 and 36 months after randomisation.
In addition, an endothelial independent vasodilatation test (NTG) using nitroglycerine sublingually, was performed at baseline and at 36 months after randomisation. The NTG measurements were performed without withholding of used medications.
2.2 Study population
The population enrolled in the PERFECT study is similar to that enrolled in the EUROPA trial . In short, the main inclusion criteria are 18 years of age or above; documented coronary artery disease, not scheduled for re-vascularisation and informed consent obtained. Documented coronary heart disease includes a history of previous myocardial infarction (confirmed by ECG demonstrating Q waves in two contiguous leads and/or changes in cardiac enzymes more than or equal to twice the normal values) of at least 3 months prior to the selection visit, or, a history of PTCA or CABG of at least 6 months prior the selection visit, or, abnormal findings at coronary angiography (angiographical evidence of ≥70% narrowing of ≥1 major coronary artery according to visual analysis). Also, men with a history of chest pain documented by either a positive exercise test or by the development of regional wall motion abnormalities during stress echocardiography or nuclear scintigraphy or perfusion defects during scintigraphy perfusion imaging could be included.
The main exclusion criteria were clinical signs of heart failure requiring treatment; systolic blood pressure <100 mmHg; uncontrolled treated hypertension with systolic blood pressure >180 mmHg and/or a diastolic blood pressure >100 mmHg; use of ACE inhibitors or angiotensin II receptor inhibitors within 1 month prior to the first selection visit; renal failure with serum creatinine >150 μmol/l; serum potassium >5.0 mmol/l; liver disease with liver enzymes >3 times upper normal values; a history of stroke or cerebral transient ischaemic attacks within the preceding 3 months and known intolerance to ACE inhibitors.
All patients who participated in the main EUROPA study and had been enrolled in study centres that participated in the PERFECT study, were additionally invited to participate in the PERFECT study. All those patients that were willing and gave informed consent were considered as PERFECT participants. Since refusal rates for PERFECT were assumed to be independent of the treatment assignment, it was expected that the PERFECT participants would resembles closely the EUROPA participants.
2.3 PERFECT study measurements
The study outcomes were (1) absolute change in FMD percentage of the brachial artery between the 36 month measurement and the baseline measurement, (2) absolute change in FMD percentage of the brachial artery between the 6 month measurement and the baseline measurement, (3) Rate of change in FMD in 36 months.
2.4 Assessment of brachial artery flow mediated vasodilatation (FMD)
Preceding the start of the PERFECT study, a detailed training programme was implemented to ensure standardisation of the FMD measurements across all centers. Based on the performance during and after the training programme all sonographers entered the certification procedure.
Ultrasound examinations were performed using a Duplex scanner with a >7 MHz or 7–10 MHz linear array transducer, with on line ECG recording. The examinations were recorded on (S-)VHS videocassette and sent to a core laboratory for off line reading. The details of the measurement have been detailed elsewhere . In short, patients were studied in supine position. Three ECG leads were attached. The arm was placed in a specifically developed splint to reduce arm movements during the procedure as much as possible and to allow for fixation of the ultrasound transducer. The blood pressure cuff was placed just below the elbow, and below the ultrasound transducer. After a 10 min rest, the brachial artery at the elbow was visualised using a ultrasound machine with a >7 MHz or 5–10 MHz linear array transducer. When a satisfactory longitudinal optimal image of the brachial artery was obtained, the position of the transducer was fixed in the holder. Three B-mode images showing the lumen diameter were frozen on the R-wave of the ECG to provide information for off-line measurement of the ‘baseline’ lumen diameter for the ischemia test. Then the blood pressure cuff was inflated to suprasystolic levels (50 mmHg above) for a four-minute period. During that time the sonographer checked whether the optimal image was steady. After deflation of the blood pressure cuff, ultrasound examination continued for 5 min. Every 15 s a B-mode image was frozen on the R-wave of the ECG (end-diastole) for off-line lumen diameter measurements [20, 21].
At baseline and at month 36 the effect of nitroglycerine was evaluated after the ischemia test using a similar procedure as described above. When a satisfactory longitudinal optimal image of the brachial artery was obtained, three B-mode images showing the lumen diameter were frozen on the R-wave of the ECG to provide information for off-line measurement of the ‘baseline’ lumen diameter for the nitroglycerine test. Then 400 μg of nitroglycerine were sublingually administered. The ultrasound examination continued for another 5 min. Every 15 s a B-mode image was frozen on the R-wave of the ECG (end-diastole) for off-line lumen diameter measurements.
The off line reading of the PERFECT Study ultrasound examinations was done using Brachial Tools®, version 3.2.6 (Medical Imaging Applications, Iowa, USA). In short, first the frozen images on videotape are digitised and put into a time sequence. Then the reader manually identifies the part of the brachial artery in which the boundaries are good and stable visualised in all these images. Next, the Brachial Tools® software detects the boundaries through all these images and provides numerical data on lumen diameters of all the images. The diameter at baseline was based on the average of the three frozen images. FMD was estimated as [maximal lumen diameter after ischemia − diameter at baseline]/diameter at baseline. The nitroglycerine response (flow independent vasodilatation) was estimated as [maximal lumen diameter after nitroglycerine − diameter at baseline]/diameter at baseline.
2.5 Sample size considerations
At the start of the preparations of the PERFECT study in 1998, an estimate of what was considered a clinically relevant difference in FMD from baseline varied between 1.8 and 6.7% in the published literature. In a study among subjects who underwent coronary angiography, the positive predictive value of FMD less than 3% in predicting coronary endothelial dysfunction was 95% . It had been argued that in clinical trials the number of subjects needed should be such that at least a 2% difference in FMD is detectable . In an earlier study performed by our group, among 32 healthy volunteers the mean FMD was 7.7% (SD 5.0) . Since the present study is a multi-centre which generally increases the variability in the FMD measurements compared to single-centre studies, the sample size calculation is to be considered conservative.
With a 90% power, a two-sided alpha of 5%, an absolute difference in FMD of 2.0% can be assessed with a sample size of 131 subjects in each arm of the trial. With an anticipated 10% drop-out rate in the EUROPA trial, a total of 288 subjects needed to be randomised.
2.6 Data analysis
General characteristics of the study population were given according to the intention to treat principle (ITT). The ITT population comprised patients who had a 6 month FMD measurement for the analyses on 6 month change in FMD. For 36 month change the ITT population comprised patients with 36 month FMD data. For the rate of change analyses, the ITT population comprised of all those patients who had at least one 6 month baseline FMD value. Those patients who had no follow-up FMD measurements or those who had inadequate measurements were excluded for the statistical analyses. Absence to compliance of treatment was not a reasons to exclude patients from the analyses.
For each patient the difference in FMD at 6 month and baseline was calculated (FMD value at 6 months − FMD value at baseline). A similar approach was used for 36 month difference in FMD. Next, linear regression analyses were applied to study whether the 6 month or 36 month differences in FMD differed between treatment groups using difference in FMD as dependent variable and treatment assignment as independent variable. No adjustments were additionally made since the treatment assignment was achieved using a randomisation procedure. These analyses were carried out using SPSS statistical package (version 12.0). This analytic approach had a priori been decided upon although we recognise that for the 36 month effects the reduction in sample size due to the absence of 36 month measurements could be considerable.
To evaluate differences in rate of change of FMD between treatment groups a random effects model was applied using SAS statistical software (version 8.1). Apart from the assumption that the change in FMD is linear over time, we made no assumptions for the intercept (random) of the model and for correlation structure (unstructured) between repeated FMD measurements. The primary model FMD percentage as outcome, and had as independent variables assigned treatment group, visit time from baseline, and the interaction term time × group assignment. Rate of change was estimated per 6 month intervals. The advantage of using a random effects model above the earlier mentioned analytic approaches is that all FMD measurements that have been performed during the study will be used in the analyses and thereby increasing the power.
Although this is a randomised controlled trial and therefore in principle adjustment for other variables is not needed, we did perform analyses where adjustments were made for study center and for those factors that were imbalanced at baseline (gender, chest pain, hypertension).
Reproducibility of the FMD measurement was assessed using the information of the FMD measurement at baseline and at the 6 month visit in the placebo group. Overall reproducibility, i.e., reflecting the combined variability due to between and within sonographer, and between and within reader and between visit aspects, was evaluated using Intraclass correlation coefficient.
General characteristics of the PERFECT study population by assigned treatment
Perindopril (n = 167)
Placebo (n = 166)
Female gender (%)
Medical history (%)
Previous myocardial infraction
History of chest pain and positive exercise test
Peripheral arterial disease
Current drug use (%)
History of hypertension (%)
Heart rate (bpm)
Current smoking (%)
Total cholesterol (mmol/l)
Brachial artery measurements
Baseline diameter FMD (mm)
Maximal diameter FMD (mm)
NTG response (%)
Baseline diameter NTG (mm)
Maximum diameter NTG (mm)
The mean change in FMD between baseline and 36 months was 0.91% (SD 3.77) in the perindopril group and 0.35% (SD 3.63) in the placebo group. The change in FMD of the brachial artery between the 36 month measurement and the baseline measurement was 0.55 % (95% confidence interval −0.42 1.47; p value 0.23) higher in the perindopril group compared to placebo. This statistically non-significant difference constitutes a relative improvement in FMD of 20% (=0.55/2.74). This analysis was based on measurements available at both baseline and 36 month of 256 participants. Adjustment for center or for imbalances at baseline did not materially affect the magnitude, direction or significance of the intention-to-treat estimate.
The change in flow-mediated vasodilatation of the brachial artery between the 6 month measurement and the baseline measurement between treatment groups was −0.12% (95% CI −0.87, 0.85; p value 0.97). This analysis was based on measurements available at both baseline and 6 months of 294 participants. Adjustment for center or for imbalances at baseline did not materially affect the magnitude, direction or significance of the intention-to-treat estimate.
No difference in nitroglycerine response results at 36 months was found between perindopril and placebo. Mean values (SD) were 8.2% (5.4) and 8.8% (5.4), respectively.
The PERFECT study was designed to evaluate whether long-term administration of perindopril improves endothelial dysfunction in patients with stable CAD and without clinical heart failure. Our findings, analysed in two ways, indicate that long-term use of perindopril is compatible with an improvement in FMD, although these findings were not statistically significant. The rate of change in endothelial function per 6 months showed a significant improvement over time in the perindopril group, where the comparison with placebo showed that these improvements bordered on statistical significance (p of 0.07).
The mechanisms underlying the beneficial effects of ACE inhibition are complex, and include inhibition of angiotensin II production with, subsequently, a reduction of its negative effects on the vascular system. Through coupling to the angiotensin II type 1 receptor, angiotensin II leads to vasoconstriction, vascular inflammation with an increase in pro-inflammatory genes, adhesion molecules and macrophage recruitment, an increased uptake and oxidation of LDL by endothelial cells and oxyradical production leading to endothelial dysfunction. Furthermore, it stimulates sympathetic activation and aldosterone release, adding to vasoconstriction and endothelial dysfunction. ACE inhibitors may positively affect endothelial dysfunction by decreasing angiotensin II production alone. However, equally or possibly more important is their effect on bradykinin. Through coupling to the bradykinin B2 receptor bradykinin results in NO and endothelial-derived hyperpolarizing factor. In addition it promotes prostacyclin release. As a consequence, bradykinin is not only a strong vasodilator, it also inhibits, through NO production, vascular smooth muscle cell growth and migration, improves endothelial function, inhibits the expression of cell adhesion molecules, prevents platelet adhesion, and restores the fibrinolytic balance by tPA production. As such, bradykinin effectively counteracts the deleterious effects of angiotensin II. The improvement of endothelial function with ACE inhibition is bradykinin-dependent . Of importance, not all ACE inhibitors increase bradykinin production to a similar extent. This depends, amongst other factors, on tissue affinity of the ACE inhibitor. Perindopril is one of the few ACE inhibitors with profound tissue affinity . It increases bradykinin significantly more than enalapril despite similar effects on circulating angiotensin II . Also, perindopril increases bradykinin levels at lower doses than needed to reduce angiotensin II levels . Indirectly, the pivotal role of bradykinin on endothelial function is suggested by the observation that perindopril, but not an angiotensin receptor antagonist telmisartan, improves endothelium-dependent vasodilatation, after long-term treatment despite similar anti-hypertensive effects . The PERTINENT study, another sub-study of EUROPA, provides further evidence in support for the improvement in endothelial function observed in the PERFECT study . PERTINENT studied the effect of 8 mg perindopril versus placebo after one year treatment on plasma markers of atherosclerosis, neurohormonal activation and apoptosis. A significant reduction in angiotensin II and cytokine levels was found together with a reduction in apoptosis. Of importance, bradykinin increased significantly accompanied by an increase in ecNO synthase in perindopril but not in placebo treated patients. These data from a similar patient population as in PERFECT provide evidence that pivotal mechanisms in endothelial function are improved by perindopril treatment and could lead to an improvement in endothelial function, as indicated in PERFECT.
Studies performed on the effect of ACE inhibition and endothelial function as measured by FMD of the brachial artery
Type of patient
Enalapril (n = 12)
Losartan (n = 9)
FMD improved under both treatments
Essential hypertensives versus healthy controls
Enalapril (n = 9)
FMD improved under enalapril
Nifedipine (n = 28) amlodipine (n = 28) atenolol (n = 29) nebivolol (n = 28) telmisartan (n = 29) perindopril (n = 28)
FMD improved under perindopril only
Stable heart failure
Ace inhibition plus candersatan (n = 14)
Ace inhibition plus placebo (n = 14)
No difference in FMD
High fat/low fat/fenofibrate
No effect of FMD
Cross over RCT
Type II diabetes
Losartan (n = 12)
Improvement of FMD
Type II diabetes/healthy controls
No difference in FMD
Cross over RCT
Stable CHD patients
Quinapril (n = 20) enalapril (n = 20) losartan (n = 20) amlopidine (n = 20)
FMD improved only under quinapril
Cross over RCT
Type I diabetes
Perindopril (n = 20)
No effect on FMD of perindopril
Quinapril (n = 9)
Improvement in FMD
Cross over RCT
Quinapril (n = 30) losartan (n = 30)
No improvement in basal FMD , improvement in postprandial FMD reduction
Enalapril (n = 46)
Placebo (n = 45)
No effect on FMD
Some aspects of the study need some consideration to appreciate the findings. Firstly, the initial sample size estimation was based on assumptions that came from cross-sectional studies, since longitudinal data were not available. When we perform a posterior power calculation based on the availability of 240 subjects using actually observed data on the difference between baseline and 36 months in FMD in the control arm (0.35% with a SD 3.63), we had a 80% power to detect a difference in change from baseline between the perindopril group and the placebo group of 1.3%, assuming a two sided alpha of 0.05. Our power to detect a 2% difference, as was originally proposed, was even higher. However, our power to detect the currently observed difference of 0.55% was only 20%, suggesting that we can not really exclude the fact that perindopril may have an effect on endothelial function. Secondly, it has been documented that the value of FMD measurement may be affected considerably by life style habits, such as recent physical activity, smoking, and food intake, technical aspects of the measurement, such as cuff location, and concomitant drug treatment, such as statins [45–48]. Furthermore, the reproducibility of the FMD measurement in situations where lifestyle factors were controlled optimally, may be moderate with coefficients of variation between 25–50%, indicating that within person variability may be considerable . This in general leads to attenuation of the magnitude of the relations under study. Although in PERFECT a uniform training and FMD methodology was used, the study was a multicenter trial, which compared to single center studies generally increases variability as shown by our reproducibility findings. This was one of the reasons we applied a random effect model to increase the power of the study to detect meaningful differences between treatment arms.
The baseline FMD value in our population was low, similar to that found in other studies in CAD patients , and may indicate the presence of endothelial dysfunction in this group. The effect of ACE inhibition on FMD over time was modest, although significant. This may be partially attributed to the fact that most of our patients were using multiple drugs that improve endothelial function as well, for example statins . This may have reduced our ability to demonstrate the full benefit of ACE inhibition per se.
In conclusion, appreciating the variability in the FMD measurement and the widespread use of other drugs that may affect FMD, our findings are compatible with the notion that the beneficial effects of perindopril on cardiovascular morbidity and mortality in the EUROPA study may be at least partly explained by an improvement in endothelial function.
Participating PERFECT centers
CZECH REPUBLIC: CESKY KRUMLOV: J. Florian, MD (principal investigator), V. Kuchar, MD; BRNO: B. Semrad, MD (principal investigator), J. Ziembova, MD, J. Schildberger, MD; PILSEN, H. Rosolova, MD (principal investigator), V. Jankovych, MD; PRAQUE: R. Spacek, MD (principal investigator), P. Stanka; PRAQUE: J. Hradec, MD (principal investigator), J. Malik, MD; TABOR: J. Charouzek, MD (principal investigator) V. Jirka, MD; PRAGUE: P. Jansky (principal investigator), Koelbel, MD; SLANY: G. Marcinek, MD (principal investigator), M. Votypka-Pecha; BRNO: L. Groh (principal investigator), I. Hofirek, L. Nechvatal. GERMANY: MUNICH: C. von Schacky, MD, PhD (principal investigator), S. Stoerk, MD, P. Markov. GREECE: ATHENS: Gialavos, MD, (principal investigator), A. Androulakis, MD; ATHENS: J. Lekakis, MD, C. Papamichael, MD. NETHERLANDS: HARDERWIJK: R. Dijkgraaf, MD (principal investigator), Y.Jansen-Timmer, H. Bralts; HENGELO: J.J.J. Bucx, MD (principal investigator until 01/01/2000), H. Droste, MD (principal investigator from 01/01/2000), G. Assink; EMMEN: L.F.M. van de Merkhof, MD (principal investigator), R. Vinke; ROTTERDAM: van Nierop, MD (principal investigator), I.M. Toonder, E. Korten. POLAND: KRAKOW: A.Gackkowski, MD (principal investigator); KRAKOW: T. Zielinsky, MD (principal investigator), T. Rywik, MD; KATOWICE: A.M. Wnuk-Wonjar, MD (principal investigator), C. Vita; KATOWICE: M. Tendera, MD (principal investigator), M. Kazmierski; SWEDEN: MALMO: J. Persson, MD (principal investigator), G. Osting;
Endothelial function core laboratory
Vascular Imaging Center Utrecht, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands. Michiel Bots, MD, PhD; Ronald P. Stolk, MD, PhD; Rudy Meijer, Dicky Mooiweer-Bogaerdt ; Frank Leus, Brigitte Wernert, Eefje Spithoven, (http://www.juliuscenter.nl/research facilities/vascular imaging center)
EUROPA Executive Committee
Bertrand M, Ferrari R, Fox K, Remme W.J, Simoons M.
EUROPA Steering Committee
Aldershville J, Denmark; Hildebrandt P, Bassand JP, France; Cokkinos D, Greece; Toutouzas P, Greece, Eha J, Estonia; Erhardt L,Sweden; Erikssen J, Noway; Grybauskas R, Lithuania; Kalnins U, Latvia; Karsch K, Sechtem U, Germany; Keltai M, Hungary; Klein W, Austria; Luescher T, Switzerland; Mulcahy D, Ireland; Nieminen M, Finland; Oto A, Ozsaruhan O, Turkey; Paulus W, Belgium; Providencia L, Portugal; Remme W J, the Netherlands; Riecansky I,Slovakia; Ruzyllo W, Poland; Santini U, Tavazzi L, Italy; Soler-Soler J, Spain; Widimsky P, Czech Republic.
The PERFECT study is supported by a grant (protocol no CL3-O949O-144) from Institut de Recherches Internationales SERVIER (IRIS), Paris, France.