Netherlands Heart Journal

, Volume 20, Issue 1, pp 24–32

Individualised therapy of angiotensin converting enzyme (ACE) inhibitors in stable coronary artery disease: overview of the primary results of the PERindopril GENEtic association (PERGENE) study

  • J. J. Brugts
  • M. P. M. de Maat
  • A. H. J. Danser
  • E. Boersma
  • M. L. Simoons
Open AccessReview Article

DOI: 10.1007/s12471-011-0173-6

Cite this article as:
Brugts, J.J., de Maat, M.P.M., Danser, A.H.J. et al. Neth Heart J (2012) 20: 24. doi:10.1007/s12471-011-0173-6


In patients with stable coronary artery disease (CAD) without overt heart failure, ACE inhibitors are among the most commonly used drugs as these agents have been proven effective in reducing the risk of cardiovascular events. Considerable individual variations in the blood pressure response to ACE inhibitors are observed and as such heterogeneity in clinical treatment effect would be likely as well. Assessing the consistency of treatment benefit is essential for the rational and cost-effective prescription of ACE inhibitors. Information on heterogeneities in treatment effect between subgroups of patients could be used to develop an evidence-based guidance for the installation of ACE-inhibitor therapy. Obviously, therapy should only be applied in those patients who most likely will benefit. Attempts to develop such treatment guidance by using clinical characteristics have been unsuccessful. No heterogeneity in risk reduction by ACE inhibitors has been observed in relation to relevant clinical characteristics. A new approach to such ‘guided-therapy’ could be to integrate more patient-specific characteristics such as the patients’ genetic information. If proven feasible, pharmacogenetic profiling could optimise patients’ benefit of treatment and reduce unnecessary treatment of patients. Cardiovascular pharmacogenetic research of ACE inhibitors in coronary artery disease patients is in a formative stage and studies are limited. The PERGENE study is a large pharmacogenetic substudy of the EUROPA trial, aimed to assess the achievability of pharmacogenetic profiling. We provide an overview of the main results of the PERGENE study in terms of the genetic determinants of treatment benefit and blood pressure response. The main results of the PERGENE study show a pharmacogenetic profile related to the treatment benefit of perindopril identifying responders and non-responders to treatment.


PharmacogeneticsACE inhibitorsPerindoprilGeneHaplotypePolymorphismCoronary artery diseaseSecondary prevention

The angiotensin-converting enzyme (ACE) inhibitors competitively block the conversion of angiotensin-I (AT-1) into angiotensin-II (AT-II). This blockade results in a decrease in circulating and local levels of AT-II, thereby inhibiting the main effects of AT-II which are arteriolar vasoconstriction and water and salt retention. ACE inhibitors decrease the transformation of bradykinin in inactive peptides, thereby increasing the levels of bradykinin [1, 2]. The increase in levels of bradykinin leads to a higher release of nitric oxide and prostaglandins with vasodilatory effects on vessel walls [2, 3].

The efficacy of ACE inhibitors has been demonstrated by several large clinical trials in a broad variety of patients at different levels of risk [411]. Nowadays, the use of ACE inhibitors is recommended in guidelines on the management of hypertension, stable coronary artery disease (CAD), myocardial infarction (MI), and heart failure, and therefore ACE inhibitors are among the most frequently prescribed drugs in these patient groups [1214].

This review is primarily focused on patients with stable CAD and the ACE inhibitor perindopril as studied in the EUROPA trial and its substudy the PERGENE study [10, 15].

The EUROPA trial

The EURopean trial On reduction of cardiac events with Perindopril in patients with stable coronary Artery disease (EUROPA) studied the ACE inhibitor perindopril in a population with stable coronary artery disease with preserved left ventricular function [10]. In EUROPA, 12,218 patients were randomly assigned perindopril 8 mg once daily (n = 6110) or matching placebo (n = 6108). The primary endpoint was a composite of cardiovascular mortality, myocardial infarction, or cardiac arrest. During a mean follow-up of 4.2 years, perindopril was associated with a reduction in the incidence of the primary endpoint from 9.9% in placebo to 8.0% in perindopril-treated patients, which yielded a 20.5% relative risk reduction (HR 0.80; 95% CI 0.71–0.91) (Fig. 1) [10].
Fig. 1

Treatment benefit of perindopril on primary endpoint and selected secondary endpoints in the EUROPA trial. MI=myocardial infarction. UA=unstable angina. Size of squares proportional to number of patients in that group. Dashed line indicates overall relative risk reduction. Adapted with permission (Lancet 2003; 362: 782–88)

One would like to guide such prolonged prophylactic treatment to only those patients who will encounter treatment benefit. Heterogeneity in the clinical treatment effect of ACE inhibitors might be used to guide ACE inhibitor therapy only to those patients most likely to benefit from such therapy and, by doing so, the overall clinical efficacy could be increased (lower number needed to treat). Tailored ACE inhibitor therapy will improve patient benefit, and reduce unnecessary healthcare costs and side effects. Several analyses have been performed to test the consistency of the treatment benefit of ACE inhibitors among patient subgroups based on clinical characteristics which are discussed below [1620].

Guiding ACE inhibitor treatment based on clinical characteristics

Using the EUROPA trial data, a risk model based on baseline clinical characteristics related to the primary endpoint was developed to predict outcome in these patients depending on the patient’s baseline risk [17]. However, the treatment benefit of perindopril was consistent across different risk categories and therefore not modified by the level of baseline risk. Another post-hoc analysis of the EUROPA study demonstrated that renal insufficiency does not modify the treatment benefit of ACE inhibitors [18, 19]. Finally, in a recent meta-analysis which combined several trials investigating the ACE inhibitor perindopril in 29,463 patient with vascular disease (stable CAD, cerebrovascular disease and diabetes), a consistent treatment effect of ACE inhibitor based regimens was demonstrated, independent of clinical characteristics or baseline blood pressure levels (Fig. 2) [20]. We have concluded that, although many studies have been performed to test the heterogeneity of treatment benefit of ACE inhibitors in patients with stable CAD, based on these studies it does not appear to be feasible to guide ACE inhibitor therapy to specific subgroups of patients based only on clinical characteristics.
Fig. 2

Consistency of treatment benefit of perindopril in patients with vascular disease (meta-analysis of ADVANCE, PROGRESS, EUROPA individual data). MI=myocardial infaction, CVA=cerebrovascular accident, TIA=transient ischaemic attack. Adapted with permission from Brugts JJ et al. Eur Heart J 2009; 30, 1385–1394

New approaches to guiding ACE inhibitor therapy

We used more patient-specific characteristics such as patients’ genetic information (DNA). Pharmacogenetics is aimed to understand why some drugs work better for some people than others and why some people are more likely to experience side effects. If genetic factors are indeed related to drug response, pharmacogenetic profiling might be a new way to reach significant advances in individualised cardiovascular medicine.

Currently, pharmacogenetic research of ACE inhibitors is rare. In general, it is expected that the response of a patient to therapy can be influenced by several types of genetic factors: 1) Genetic factors causing differences in drug absorption and metabolic clearance are highly relevant (pharmacokinetics); however; this is still a relatively unexplored field for ACE inhibitors. 2) Genetic factors within the direct pharmacodynamic pathway that is affected by the ACE inhibitors, the renin–angiotensin–aldosterone system (RAAS), and bradykinin gene pathways are likely to affect the clinical efficacy of ACE inhibitors, including receptors and signal transduction molecules. Also, variations within genes of the RAAS and related systems may influence atherosclerosis and thereby inherent differences in the susceptibility to the antiatherosclerotic properties of ACE inhibitors [21, 22].

The vast majority of prior studies focused on only one or two polymorphisms, the angiotensin-converting enzyme (ACE) I/D polymorphism and the M235T polymorphism in the angiotensinogen (AGT) gene. This is a severe limitation and does not justify the complexity of the renin-angiotensin system. Because of limited study sample size and power, results have been inconsistent. Limited prior research with ACE inhibitors in stable CAD has been performed at large-scale or in a randomised trial setting.

Concept of pharmacogenetic research to individualise medicine

The concept of pharmacogenetic research to individualise medicine is emerging rapidly and is clinically highly relevant. Several successes of this approach have recently been demonstrated for different cardiovascular agents, such as the activation of clopidogrel [23, 24] and the risk of rhabdomyolysis associated with statin therapy [25]. Current pharmacogenetic data are often obtained from observational cohort studies or cross-sectional data. The overall objective of CVD pharmacogenetics is to construct a genetic profile which enables the doctor to predict the patient’s benefit of treatment in advance, before subscription or during subscription when patients response is different from expected.

The PERGENE study

The PERindopril GENEtic association study (PERGENE) is a pharmacogenetic substudy of the main EUROPA trial [15]. The PERGENE study aims to assess the practicability of pharmacogenetic profiling of treatment benefit of ACE inhibitors in patients with stable CAD for reasons addressed above. We hypothesised that genetic polymorphism in the RAAS and kininogen–kallikrein–bradykinin pathways influences the treatment benefit of ACE inhibitors in patients with stable CAD. The main outcome measure of PERGENE was the interaction between genetic factors and treatment effect of ACE inhibitors during follow-up. Secondary endpoint was the relation between the genetic determinants and blood pressure and blood pressure reduction to ACE inhibitor therapy [15].

Study design

Exact details on the study design, SNP selection procedure and statistical analysis can be found elsewhere [15]. In brief, the PERGENE study investigates whether common genetic variation is related to the risk of future events and modifies the treatment effect of perindopril. Written informed consent for performing genetic association analyses was obtained from all patients. A DNA bio-bank was established within the EUROPA trial (at the beginning of the EUROPA study) for the PERGENE substudy [15]. Blood samples were received from 10,060 patients and DNA was successfully isolated from 9454 patients using an automated isolation process (Hamilton NV, USA). Twelve candidate genes within the direct pharmacodynamic pathway of ACE inhibitors, the RAAS and bradykinin systems, were selected for this analysis (Fig. 3). To cover common variation in these 12 candidate genes comprehensively, haplotype-tagging SNPs (ht-SNP) were selected based on the linkage disequilibrium (LD) structure as provided by the public databases of HapMap, PARC, and SeattleSNPs.
Fig. 3

Selected candidate genes in the renin–angiotensin–aldosterone system and bradykinin pathways. AGT angiotensinogen, REN renin, ACE angiotensin-converting enzyme, AGTR1 angiotensin II receptor type 1, AGTR2 angiotensin II receptor type 2, CYP11B aldosteron synthase, KLK kallikrein, KNG kininogen, BDKRB1 bradykinin receptor type 1, BDKRB2 bradykinin receptor type 2, eNOS3 nitric oxide synthase. Adapted with permission from Brugts JJ et al. Cardiovasc Drugs Ther 2009;23:171–181

The treatment effect of perindopril was defined as the reduction in the event rate of the primary endpoint of the EUROPA trial compared between genotype strata for each SNP. Genotype-treatment interactions were assessed with multivariate Cox proportional hazards regression models. Multiple testing corrections of treatment interaction terms, and estimation of empirical P-values, were implemented using Monte Carlo permutation analysis (10,000 permutations) on a per-gene basis.

Results of the PERGENE study

Pharmacogenetic determinants of clinical treatment effect of ACE inhibitors

In unadjusted analysis, 7 single nucleotide polymorphisms in 4 different candidate genes were significantly associated with the treatment effect of perindopril. In multivariate permutation analysis, 3 of these SNPs, located in the AT1 receptor and BK1 receptor genes, remained significant modifiers of the treatment benefit of perindopril [26].

In the BK1 receptor gene, rs12050217 was a strong modifier of the treatment benefit of perindopril as presented in Fig. 4. Additionally, in the AT1 receptor gene, rs275651 and rs5182 significantly modified the treatment benefit of perindopril. Genetic determinants of treatment benefit of perindopril have not been demonstrated previously [26].
Fig. 4

Treatment effect modifying SNPs in PERGENE. 1/1=homozygous common allele, ½=heterozygous, 2/2=homozygous common allele. Percentages correspond to the number of patients within each group according to genotype. The X-axis corresponds to the hazard ratio and 95% CI estimates and Y-axis to genotype category. Adapted with permission from Brugts JJ, et al. Eur Heart J. 2010 Aug;31(15):1854–64

We constructed a pharmacogenetic risk score by combining the unfavourable alleles of the treatment effect modifying SNPs (Fig. 5) [26]. Unfavourable alleles were associated with diminished treatment effect as observed in the overall study group. The pharmacogenetic risk score demonstrated a decrease in the level of treatment benefit of perindopril with an increasing number of unfavourable alleles. In patients with no unfavourable alleles, a much more pronounced treatment benefit was observed as compared with the overall study result (which yielded a 20% relative risk reduction). By combining pharmacogenetic risk scores, we observed that the treatment benefit was concentrated in about 3 out of 4 of the patients and absent in 1 out of 4 of the patients [26]. This is the first time that subgroups of responders and non-responders to ACE inhibitor treatment have been identified. An interaction effect of similar direction and magnitude was observed in an initial confirmatory analysis of 1051 patients with cerebrovascular disease from the PROGRESS trial [26].
Fig. 5

Treatment effect according to the pharmacogenetic profile categories. Responders=<3 unfavourable alleles, non-responders ≥3 unfavourable alleles. Adapted with permission from Brugts JJ, et al. Eur Heart J. 2010 Aug;31(15):1854–64

In the patients who were identified as responders and non-responders with pharmacogenetic profiling, no differences in clinical characteristics were observed in PERGENE [26]. Also intermediate phenotypes such as blood pressure and blood pressure reduction levels were comparable between responders and non-responders [26]. Thus, the observed treatment interaction cannot be explained by clinical differences between the genotypes but can only be prescribed to the net genetic difference between patients.

RAAS genes in relation to hypertension and blood pressure reduction to ACE inhibitors

As hypertension is a strong intermediate phenotype of CAD, we investigated whether genetic variations in the cascade of RAAS/bradykinin system genes are involved in blood pressure and whether such genetic variations determine the BP response to ACE inhibitor therapy which is highly variable between patients [27]. A differential BP effect determined by genetic factors may give insight into their clinical effects.

The PERGENE study demonstrated that the genetic variants in the ACE, angiotensinogen and prorenin gene were important determinants of hypertension at baseline. These genetic determinants of hypertension in the RAAS system were also observed in the two replication cohorts of the PROGRESS trial (patients with cerebrovascular disease) and ERGO study (relatively healthy elderly subjects) [27] (Fig. 6). However, the blood pressure response to the ACE inhibitor perindopril was not modified by the genetic polymorphisms in the RAAS or bradykinin pathway.
Fig. 6

Cumulative effects of the identified SNPs on the prevalence of hypertension. OR hypertension. OR odds ratio CI confidence interval. Adapted with permission from Brugts JJ, et al. J Hypertens. 2011 Mar;29(3);509–19

These findings are consistent with prior subgroup analyses on blood pressure and BP reduction by ACE inhibitor therapy demonstrating that the clinical benefits are independent of blood pressure and the amount of BP reduction [20, 28, 29].

To strengthen our results, the Blood Pressure Lowering Treatment Trialists’ Collaboration (BPLTTC) consortium studied the blood pressure dependent and independent effects of ACE inhibitors in 146,838 patients and confirmed that a beneficial effect up and above blood pressure reduction is present [29]. Substudies of EUROPA have investigated the additional effects of ACE inhibitors and have established that ACE inhibitors have additional effects beyond the blood pressure reduction alone, such as the improvement of endothelial function, improvement of the neurohumoral balance, and reduction of unfavourable remodelling of the coronary arteries [30, 31].

Potential mechanisms of the pharmacogenetic profile of treatment benefit

In summary, the PERGENE study identified new genetic determinants of clinical treatment benefit of ACE inhibitors, but these genetic determinants do not mediate these effects through change in BP as these SNPs did not pop up in the analysis on BP reduction [26, 27]. The treatment effect modifying SNPs was particularly located in the AT1 and BK1 receptors. The SNPs in the AT1 receptor were located in the promoter (rs275651) and exon 4 (rs5182) on chromosome 3, the SNP in the BK1 receptor gene on chromosome 14 was located in an intron region. All three SNPs were important tagging SNPs within their candidate gene [26]. Functionality of these SNPs is at this moment unknown, but more basic research has been started based on these findings. As the AT1 receptor is involved in the direct effects of angiotensin II, it can be hypothesised that genetic variants in the AT1 receptor will influence the response to an ACE inhibitor. The exact role of the BK1 receptor, on the other hand, is less well established. Bradykinin is a potent vasodilator that also induces antiatherosclerotic and antithrombotic effects, which are mediated by BK2 receptors. Previous studies indicated that the clinical benefit of ACE inhibitors depends, at least in part, on BK2 receptor activation [32]. In the past year, more data are emerging on the effect of the BK1 receptor, the effects of which are less well known. BK1 receptors are weakly expressed under physiological conditions, but are strongly induced in response to pathological conditions and/or RAAS blockade [33, 34]. Recent reports indicate that BK1 receptor deficiency predisposes to atherosclerosis [35] and kinins and the BK1 receptor plays an important deleterious role in this process [36]. Interestingly, it has been suggested that BK1 receptors are directly activated by ACE inhibitors (thus resulting in an increase in endothelial NO release, for instance in the heart [37, 38], by which they do contribute to the cardioprotective beneficial effects of ACE inhibitors, but this has not been uniformly confirmed by others [39]. Therefore, a more likely possibility is that the upregulated BK1 receptors are activated by their endogenous ligand during ACE inhibition. Such activation results in the hypotensive [40], cardioprotective [37] and cerebroprotective [41] effects of kinins, as observed in animals, and one could speculate that patients with genetic defects in their BK1 receptor display a diminished response to ACE inhibition with regard to kinins. Indeed, in our study we observed that especially patients with the minor allele variants of the BK1 receptor were relatively insensitive or resistant to the beneficial effect of the ACE inhibitor. Clearly, more work is needed to support this interesting concept.

Still, the lack of a blood pressure related effect of the 3 identified SNPs in the treatment effect analysis suggests a different pathway of clinical effect [26, 27] and emphasises more on the bradykinin effects of ACE inhibitors as the blood pressure independent effects of ACE inhibitors is often proposed for the BK pathway [11]. Our analyses may indicate that the up-regulated BK1 receptor in stressed CAD patients may play an important role in the assumed pleiotropic effect of ACE inhibitors. Our findings do support that concept, as it might be speculated that the genetic defects in the BK1 receptor alter the antiatherosclerotic properties of the ACE inhibitor treatment effect which might be an important cornerstone of the treatment benefit besides blood pressure lowering.

Clinical implications: pharmacogenetic breakthrough in the rationale of prescribing medication

The PERGENE study demonstrated a relative resistance to ACE inhibitors in patients with unfavourable alleles of the AT1 receptor and BK1 receptor genes. Based on the PERGENE findings, three out of four patients with stable CAD (participating in EUROPA) had an enhanced benefit of ACE inhibitor therapy, and one out of four patients experienced a markedly diminished benefit of treatment with perindopril (non-responders, risk score ≥3).

In our pharmacogenetic profile (Table 1) categories of patients with <3 and ≥3 unfavourable alleles, relative risk reduction was 33% (HR 0.67; 95% CI 0.56–0.79) and +26% (HR 1.26; 95% CI 0.97–1.67), respectively. Refraining from treatment with perindopril in this group of patients may considerably reduce healthcare costs and increase overall efficacy of the drug.
Table 1

Hazard ratios for the pharmacogenetic risk scores and clinical treatment benefit of the ACE inhibitor perindopril

Risk scores

Number of patients (%)

Hazard ratio (95% CI)



0.58 (0.46–0.72)



0.81 (0.63–1.03)



1.26 (0.97–1.67)

Pharmacogenetic profile



0.67 (0.56–0.79)



1.26 (0.97–1.67)

Overall study


0.80 (0.71–0.91)

In the fictive scenario that only patients with <3 unfavourable alleles would have been treated, which compromises 76.5% of the population, the absolute risk would be reduced from 11.1% in placebo to 7.5% in perindopril patients. Likewise, the number needed to treat would decrease from 50 to 32. Considering the millions of patients treated with ACE inhibitors, this reduction has huge clinical implications and fictively demonstrates the potential of pharmacogenetic profiling of drug response to antihypertensives.

Feasibility of pharmacogenetic profiling of ACE inhibitors

The PERGENE study is one of the first pharmacogenetic analyses within a randomised clinical trial demonstrating the heterogeneity in treatment benefit of ACE inhibitors. These promising results indicate that the concept of pharmacogenetic profiling is feasible and should be investigated more. Further replication must be sought in other cohorts and replicated in similar patient populations but also in patients at higher risk of events. Additionally, other relevant genetic targets need to be investigated such as genes involved in the metabolism of ACE inhibitors, fe CYP450 genes (pharmacokinetics). However, until now no specific genetic targets for ACE inhibitor metabolism have been demonstrated.

We advocate that future large-scale randomised clinical trials should also integrate a pharmacogenetic analysis in their trial design to prospectively test treatment efficacy in a similar way. Pharmacogenetic analyses of clinical trials truly open up a perspective to individualise preventive therapy in patients with cardiovascular disease. Physicians will be able to predict the response to treatment (responders and non-responders) in advance, before starting prescription. ‘Individualised therapy’ by pharmacogenetic profiling will avoid unnecessary treatment of non-responding patients and considerably reduce healthcare costs.


Brugts is supported by a grant from the Netherlands Heart Foundation (NHS-2005-B219) and a grant from the Netherlands Organization for Health Research and Development (ZonMW).

Financial disclosure


Conflict of interest

JJB, MM, JD and EB declare to have no conflict of interest, MLS has received speaker fees and research grants from Servier.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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© The Author(s) 2011

Authors and Affiliations

  • J. J. Brugts
    • 1
  • M. P. M. de Maat
    • 2
  • A. H. J. Danser
    • 3
  • E. Boersma
    • 1
  • M. L. Simoons
    • 1
  1. 1.Department of CardiologyErasmus MC ThoraxcenterRotterdamthe Netherlands
  2. 2.Department of HematologyErasmus MCRotterdamthe Netherlands
  3. 3.Department of PharmacologyErasmus MCRotterdamthe Netherlands