Abstract
Combinations between an angiotensin converting enzyme (ACE) inhibitor or an angiotensin II receptor blocker (ARB) and hydrochlorothiazide (HCTZ) are among the recommended treatments for hypertensive patients uncontrolled by monotherapy. Four randomized, double-blind, parallel group studies with a similar design, including 1469 hypertensive patients uncontrolled by a previous monotherapy and with ≥1 cardiovascular risk factor, compared the efficacy of a combination of a sulfhydryl ACE inhibitor (zofenopril at 30 or 60 mg) or an ARB (irbesartan at 150 or 300 mg) plus HCTZ 12.5 mg. The extent of blood pressure (BP)-lowering was assessed in the office and over 24 h. Pleiotropic features of the treatments were evaluated by studying their effect on systemic inflammation, organ damage, arterial stiffness, and metabolic biochemical parameters. Both treatments similarly reduced office and ambulatory BPs after 18–24 weeks. In the ZODIAC study a larger reduction in high sensitivity C reactive protein (hs-CRP) was observed under zofenopril (−0.52 vs. +0.97 mg/dL under irbesartan, p = 0.001), suggesting a potential protective effect against the development of atherosclerosis. In the ZENITH study the rate of carotid plaque regression was significantly larger under zofenopril (32% vs. 16%; p = 0.047). In the diabetic patients of the ZAMES study, no adverse effects of treatments on blood glucose and lipids as well as an improvement of renal function were observed. In patients with isolated systolic hypertension of the ZEUS study, a slight and similar improvement in renal function and small reductions in pulse wave velocity (PWV), augmentation index (AI), and central systolic BP were documented with both treatments. Thus, the fixed combination of zofenopril and HCTZ may have a relevant place in the treatment of high-risk or monotherapy-treated uncontrolled hypertensive patients requiring a more prompt, intensive, and sustained BP reduction, in line with the recommendations of current guidelines.
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Introduction
Large intervention trials have shown that the majority of hypertensive patients may need a combination of two or more antihypertensive medications to achieve satisfactory blood pressure (BP) control and effective cardiovascular (CV) protection [1, 2]. This holds true particularly for patients at high risk for CV events, such as older individuals, patients with diabetes or the metabolic syndrome, co-existing CV disease, or other associated clinical conditions [3, 4]. According to the evidence provided by major intervention trials, current guidelines for the management of arterial hypertension acknowledge and recommend the use of combination treatment, particularly when BP control with initial monotherapy is inadequate [5–8].
Amongst the most effective two-drug antihypertensive combinations are those between an antagonist of the renin–angiotensin–aldosterone system (RAAS), such as an angiotensin converting enzyme (ACE) inhibitor or an angiotensin II receptor blocker (ARB), and a thiazide diuretic. The mechanism of action of such a combination implies a synergistic and opposite effect on the RAAS, in which the ACE inhibitor or the ARB antagonize the counter-regulatory system activity triggered by the diuretic, thus improving the efficacy and tolerability of single drug components [9–11].
Recently, we published four randomized, double-blind, parallel group, direct comparative studies (also called “Z” studies, because of the common initial of their acronyms: ZODIAC, ZENITH, ZAMES, and ZEUS) which were planned to gain a deeper insight into the mechanisms of the antihypertensive effects of a two-drug fixed combination between a RAAS antagonist and a thiazide diuretic [12–15]. In these non-inferiority trials, efficacy and safety of the sulfhydryl ACE inhibitor zofenopril and of the ARB irbesartan both combined with hydrochlorothiazide (HCTZ) 12.5 mg were tested in hypertensive patients with one or more CV risk factors beyond hypertension (including diabetes, metabolic syndrome, and advanced age) and not responding to a previous monotherapy. In all studies, zofenopril and irbesartan were started at a dose of 30 and 150 mg, respectively, and were increased during the course of the follow-up to 60 and 300 mg, in non-responders, in order to check the effectiveness and tolerability of a highest dose of the drugs. Efficacy was evaluated not only in the office but also over 24 h by ambulatory blood pressure monitoring (ABPM). In addition, ancillary or pleiotropic features of the study drugs were evaluated by studying their effect on inflammation, target organ damage, arterial stiffness, and metabolic biochemical parameters (blood glucose and lipids). A summary of the study designs and an overview of the number of patients included in each individual study and the main patient features are reported in Table 1. In total, 1535 hypertensives were recruited in 126 centers in six European countries (Italy, Greece, Lithuania, Romania, Turkey, and Russia). Both drugs had a similar efficacy on office and ambulatory BP but some differences between the study medications could be observed for secondary efficacy endpoints. In the ZODIAC study, treatment with the zofenopril combination was associated with a larger (p = 0.001) reduction of hs-CRP (−0.52 mg/dL) than irbesartan (+0.97 mg/dL, p = 0.001), suggesting a potential protective effect against vascular inflammation, a well-known promoter of atherosclerosis at all its stages, from the endothelial cell dysfunction to the culmination in acute coronary syndrome [16, 17]. In the ZENITH study, both treatments had a similar positive effect on regression of cardiac and renal damage, whereas a larger proportion of patients showing carotid plaque regression was observed under zofenopril (31.6% vs. 16.1%; p = 0.047), particularly in the subgroup of patients taking the low dose of zofenopril (30 mg) plus HCTZ 12.5 mg (4.7% vs 10.0% irbesartan 150 mg plus HCTZ 12.5 mg; p = 0.043). These findings further confirmed the potent antiatherosclerotic effects of RAAS blockade and in particular of zofenopril, which are mediated by its antihypertensive, anti-inflammatory, antiproliferative, and oxidative stress-lowering properties [18, 19]. In the ZAMES study, metabolic parameters and renal function were not altered by treatments, except for albumin-to-creatinine ratio (ACR), whose reduction with treatment was larger under irbesartan combined with the thiazide diuretics (−24.2 vs. −9.9 mg/g with zofenopril; p = 0.027). The metabolic neutrality of treatment documented in this large study is an important finding, given the relevant notion that thiazide diuretics may induce metabolic abnormalities and that patients with metabolic syndrome may be particularly susceptible to such effects [20]. Finally, in a subgroup of 93 elderly hypertensive patients of the ZEUS study, treatment with zofenopril or irbesartan was associated with small reductions in central SBP and arterial stiffness indices (pulse wave velocity or PWV and augmentation index or AI), which were similar between the two study drugs at any time point of the study, including the first 6 weeks when all patients were treated with the lowest dose of zofenopril or irbesartan combined with the thiazide diuretic. Though such improvements were not striking as a result of the limited vascular impairments of the patients, they are relevant, because arterial stiffness represents a late manifestation of increase elastic arterial stiffness [21], and because they are consistent with those observed in previous randomized studies with the same classes of antihypertensive agents [22–24].
Given these premises, in the next sections of this review we will briefly summarize and discuss other results of the “Z” studies, which were not presented in the original publications. These include outcomes based on low dose treatment of both study medications, pooled individual analysis of ABPM data and of safety data. This article is based on previously conducted studies and does not involve any new studies of human or animal subjects performed by any of the authors.
Efficacy in Low Dose Subgroup
As expected on the basis of the study design and objectives, most of the patients enrolled in the “Z” studies took the high dose of zofenopril (75%) and the high dose of irbesartan (69%).
In three of the four “Z” studies, the efficacy of low dose zofenopril combination (30 mg) and low dose irbesartan combination (150 mg) was also assessed: this subanalysis was compelling because the zofenopril 30 mg plus HCTZ 12.5 mg combination is at present the only marketed fixed-drug combination of zofenopril with a thiazide diuretic. Average office BP changes with treatment under the low drug doses in these studies are shown in Fig. 1. No patients were under low dose drug treatment at study end in the ZAMES study because only patients forcedly up-titrated to the high dose were kept in that study.
In the ZODIAC study at the end of the 18 weeks, office sitting DBP reductions were significantly larger (p = 0.022) with zofenopril 30 mg plus HCTZ [n = 55; 19.8 (22.8, 16.8) mmHg] than with irbesartan 150 mg plus HCTZ [n = 69; 14.5 (17.9, 11.1) mmHg], whereas they were similar for SBP [zofenopril: 25.8 (30.5, 21.2) mmHg vs. irbesartan: 22.0 (27.1, 16.8) mmHg; p = 0.274] [25]. In the patients of the ZENITH study taking the low drug doses at study end (n = 223), the proportion of responders did not differ (p = 0.693) between zofenopril (76.4%) and irbesartan (78.9%), as well as the office SBP and DBP reductions (Fig. 1) [13]. Also in the subgroup of patients with moderate–severe hypertension (office BP ≥160 mmHg and DBP ≥100 mmHg) taking the lowest dose during the study, the zofenopril combination was associated with an antihypertensive response similar to that of the irbesartan combination (88.9% vs. 80.0%; p = 0.596).
In the patients of the ZEUS study maintaining the low drug doses throughout the study (n = 77), the magnitude of the daytime BP lowering was always slightly larger under zofenopril 30 mg plus HCTZ 12.5 mg than under irbesartan 150 mg plus HCTZ 12.5 mg [14]. In this study subgroup, a statistically significant (p = 0.028) difference in favor of zofenopril-treated patients was achieved at study end [16.2 (20.0, 12.5) mmHg vs. 11.2 (14.4, 7.9) mmHg irbesartan-treated patients]. For the low dose subgroup also the percentage of patients showing daytime SBP normalization (<135 mmHg) and daytime SBP response (SBP <135 mmHg or reduction ≥10 mmHg) at study end was significantly larger under zofenopril (88.9% and 91.7%) than under irbesartan (73.2% and 78.0%; p = 0.017 and p = 0.024, respectively).
The high rate of BP control and the good BP-lowering effect observed in the “Z” studies with both RAAS antagonists at the lowest dosage confirm recommendations of current guidelines which indicate a two-drug low dose combination of an ACE inhibitor or an ARB and a thiazide diuretic as a reasonable alternative to high dose monotherapy in patients previously classified as non-responders to monotherapy [6, 7]. It also strengthens the evidence from previous large randomized studies in patients with mild–moderate hypertension, in which treatment with the low dose of zofenopril (30 mg) combined with HCTZ 12.5 mg once-daily showed a greater efficacy than the monotherapy with either agent, with an increase in the response rate up to 55–65% [26, 27].
Efficacy Over 24 h
As detailed in the publications of the individual “Z” studies, the good office BP control obtained with zofenopril and irbesartan was confirmed over 24 h by ABPM, which was available for 53% of patients included in primary endpoint analysis. In order to better assess the antihypertensive effect of the drugs over 24 h, we pooled individual ABPM data of the ZODIAC, ZENITH, and ZAMES studies, namely the “Z” studies with similar inclusion criteria (the ZEUS study included only isolated systolic hypertension or ISH patients, and selection of patients for study entry was based not only on office but also on ambulatory BP). In the 561 patients of the pooled ABPM data analysis, the 24-h antihypertensive effect was similar between the two drugs, regardless of the dose employed: 24-h SBP was reduced by 7.6 (9.5, 5.7) mmHg under zofenopril and by 9.5 (11.2, 7.7) mmHg under irbesartan (p = 0.155), whereas DBP dropped by 5.5 (6.6, 4.4) mmHg and by 6.6 (7.6, 5.5) mmHg (p = 0.170).
As shown in Fig. 2a, both drugs displayed a similarly smooth and long-lasting antihypertensive effect, with similar smoothness indices for SBP [zofenopril: 0.57 (0.41, 0.73) vs. irbesartan: 0.76 (0.61, 0.91); p = 0.100] and DBP [0.50 (0.36, 0.63) vs. 0.61 (0.49, 0.74); p = 0.217]. Interestingly, the magnitude of the 24-h BP reduction yielded by zofenopril and irbesartan in the “Z” studies was comparable with that observed in previous studies based on ABPM and making use of the same doses of the two drug combinations [28, 29].
The BP-lowering effect of the two tested drugs was also similar in the low (n = 157, 28% of patients) and the high drug dose (n = 404; 72%) subgroup, either over 24 h or in the last 6 h from the last drug intake: in this subperiod the BP reduction was still comparable between zofenopril and irbesartan and corresponded to 75–85% of the overall 24-h effect (Fig. 3).
In the low drug dose subgroup BP was effectively reduced both under zofenopril (30 mg) and irbesartan (150 mg) plus HCTZ 12.5 mg for each hour of the 24 h (Fig. 2b). Twenty-four hour BP was also similarly reduced in subgroups of high risk patients such as males, aged persons (≥55 years for males and ≥65 years for females), smokers and alcohol drinkers, patients with diabetes or impaired fasting glucose, patients with a high or very high cardiovascular risk, and patients with sustained hypertension (namely those simultaneously displaying elevated office and 24-h BP) (Table 2).
Long-Term Efficacy of the Combinations
In the ZODIAC and ZENITH studies long-term follow-up of patients treated with high dose combination at study end was planned in order to collect more information on study drug efficacy and safety. Both drugs ensured a consistent efficacy, together with a good tolerability (see next section), also in the long-term follow-up observation.
In the ZODIAC study at the end of the 18 weeks of double-blind treatment, 229 patients among those receiving high dose combination treatment entered an open-label extension phase and were followed up for an additional 14 weeks. As shown in the upper panel of Fig. 4, both SBP and DBP reductions were well maintained during long-term treatment and did not differ between the two study arms.
In the 223 patients of the ZENITH study receiving drug dose up-titration at the end of the 18 weeks of treatment and continuing the double-blind treatment for additional 30 weeks, no difference was observed in office BP response between the two treatment groups (28.6% zofenopril vs. 22.1% irbesartan; p = 0.178) [13]. As shown in Fig. 4, in these patients, office and 24-h BPs were similarly reduced under zofenopril and irbesartan combinations either at the end of the 18 weeks or at the end of the extension phase. Likewise, the impact of treatment on organ damage did not significantly differ between the two study drugs.
Tolerability of Both Drug Combinations
The overall tolerability profile of zofenopril and irbesartan in the “Z” studies was good and comparable with that in previous reports [26, 30]. The safety population consisted of 1535 patients, of which 762 received the zofenopril and 773 the irbesartan combination (Table 3). Both drugs were well tolerated, with a very limited number of adverse events, which were well balanced between the two study arms (25.2% of patients receiving zofenopril and 21.9% receiving irbesartan; p = 0.715). The percentage of drug-related adverse events was much smaller than that of overall adverse events and still homogeneously distributed between the two groups (9.4% zofenopril vs. 6.2% irbesartan; p = 0.273). In total, only 66 patients (4.3%) were withdrawn from the studies because of an adverse event, 38 in the zofenopril (4.9%) and 28 in the irbesartan treatment group (3.6%; p = 0.593). The most common drug-related adverse event observed under zofenopril was cough (1.8% of patients), whereas dizziness was the most prevalent drug adverse reaction in irbesartan-treated patients (1.4%). All these side effects could be expected with these classes of drugs. Interestingly, the prevalence of cough with zofenopril in the “Z” studies (1.8%) was very close to that observed in previous double-blind or open-label post-marketing studies including 5794 hypertensive patients (2.4%) [31]. The relatively low incidence of cough in patients receiving zofenopril might be related to its limited ACE inhibitor potency at the lung level, responsible for a lesser accumulation of bradykinin and a reduced synthesis of prostaglandins in this tissue, as found in some experimental and animal studies [31].
In the ZODIAC and ZENITH studies safety was also evaluated during a long-term follow-up under high drug dose. In the ZODIAC study, 6.3% of zofenopril-treated patients and 1.9% of irbesartan-treated patients reported a drug-related adverse event (p = 0.172) during the prolonged follow-up. No patients treated with irbesartan were withdrawn from the study during the extension phase, whereas five patients (4.5%) dropped out in the zofenopril group (p = 0.060). In the extension phase of the ZENITH study, 12.3% of patients under high dose zofenopril plus HCTZ and 11.4% under high dose irbesartan plus HCTZ reported an adverse event (p = 0.843). Treatment-related adverse events occurred in 3.8% and 3.5% of patients under the two study drugs (p = 0.859); of these patients four were definitely withdrawn from the extension phase (three taking zofenopril vs. one taking irbesartan; p = 0.368) [13].
Limitations of This Review
A major limitation of this review is that it reports mixed information from previous original publications and from new pooled data or subgroup analyses, particularly those based on ABPM data. For this reason, it may be argued that it cannot be classified either as a review or an original paper. Indeed, in our review we briefly summarized the main results of the single studies, which helped introduce the reader to the secondary results which were available at the time of the original publications, but which were only outlined or even omitted for reasons of space. The current review gave us the possibility to add this information in order to provide a comprehensive presentation of all the available data of the “Z” studies. We think that this review may help complete the large amount of information deriving from the “Z” studies, which stand amongst the largest double-blind randomized studies comparing the effect of an ACE inhibitor and an ARB in hypertensive patients with multiple risk factors not controlled by a previous monotherapy.
Conclusions
In all the “Z” studies the combination between zofenopril and HCTZ was always similarly effective as that of irbesartan plus HCTZ, and it performed well either at the lowest dose (30 mg), which is the currently marketed one, or at the highest (60 mg) dose. Zofenopril also showed some ancillary features which suggest that the fixed combination of this drug with HCTZ may have a particular place in the treatment of high-risk or monotherapy-treated uncontrolled hypertensive patients requiring a more prompt, intensive, and sustained BP reduction, in line with the recommendations of current guidelines [6, 7]. The effective BP reduction and the large proportion of responders in both treatment arms in the “Z” studies also support the findings of previous studies that, in most patients not responding to a single antihypertensive medication, combination treatment with two drugs may substantially increase the chance of response [32, 33]. Vascular protection afforded by the sulfhydryl ACE inhibitor zofenopril may be related to its direct antiatherogenic effects [19, 34, 35], both reduction of systemic oxidative stress [17, 19, 34–38] and nitric oxide deficiency [17, 19, 38, 39], and enhancement of circulating endothelial progenitor cells [36] together with improved vascular function [40, 41].
In conclusion, results of the large “Z” studies confirm that combination treatment between a drug acting on the RAAS and a thiazide diuretic should be among the preferred choices when monotherapies fail to lower BP to or below target levels, particularly in patients displaying multiple CV risk factors.
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Acknowledgements
The “Z” studies were financially supported by Menarini International Operations Luxembourg S.A., through an unconditional and unrestricted grant. Article processing charges and open access fee for the present paper were funded by Menarini International Operations Luxembourg S.A. Concerning the current review paper, the funding source did not influence or comment on planned methods, protocol, data analysis, and interpretation of the results, preparation, review, or approval of the manuscript, and decision to submit the manuscript for publication. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval to the version to be published.
Disclosures
Stefano Omboni has received honorarium from Menarini International for manuscript preparation. Ettore Malacco has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Claudio Napoli has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Pietro Amedeo Modesti has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Athanasios Manolis has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Gianfranco Parati has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Enrico Agabiti-Rosei has occasionally received grants for lectures or for scientific meeting attendance from Menarini International. Claudio Borghi has occasionally received grants for lectures or for scientific meeting attendance from Menarini International.
Compliance with Ethics Guidelines
This article is based on previously conducted studies and does not involve any new studies of human or animal subjects performed by any of the authors.
Data Availability
The datasets generated during and/or analyzed during the current study are not publicly available because they are property of the sponsor of the studies, Menarini International Operations Luxembourg S.A., but they are available from the corresponding author on reasonable request.
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Omboni, S., Malacco, E., Napoli, C. et al. Efficacy of Zofenopril vs. Irbesartan in Combination with a Thiazide Diuretic in Hypertensive Patients with Multiple Risk Factors not Controlled by a Previous Monotherapy: A Review of the Double-Blind, Randomized “Z” Studies. Adv Ther 34, 784–798 (2017). https://doi.org/10.1007/s12325-017-0497-8
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DOI: https://doi.org/10.1007/s12325-017-0497-8