Barnidipine Real-Life Efficacy and Tolerability in Arterial Hypertension: Results from Younger and Older Patients in the BASIC-HT Study
Robert Lins1, *, Caroline De Vries2
Identifiers and Pagination:Year: 2017
First Page: 120
Last Page: 132
Publisher ID: TOCMJ-11-120
Article History:Received Date: 07/07/2017
Revision Received Date: 03/11/2017
Acceptance Date: 07/11/2017
Electronic publication date: 17/11/2017
Collection year: 2017
open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The aim of this study was to compare the efficacy and tolerability of barnidipine, a strong lipophilic calcium channel blocker, in younger (≤55 for efficacy or <65 years for adverse events) versus older (>55 or ≥65 years) patients with uncomplicated hypertension.
20,275 patients received barnidipine, 10 or 20 mg/day, as monotherapy or in combination with other antihypertensive drug(s) in the observational BArnidipine real-life Safety and tolerability In Chronic HyperTension (BASIC-HT) study. Efficacy and tolerability were assessed over a 3-month period. The present paper describes results from prespecified subgroup analyses by age not reported elsewhere.
Both age groups showed a clinically meaningful decrease in blood pressure (BP) over time (p<0.0001). The mean systolic and diastolic BP after approximately 3 months of barnidipine therapy was well below the target value of <140/90 mmHg for individual patients, with no notable differences between age groups. The decrease in mean pulse pressure was greater in patients >55 years (-10.8 mmHg) than in patients ≤55 years (-8.7 mmHg) (p<0.0001) and the proportion of patients with pulse pressure >60 mmHg decreased from 61.1% at baseline to 24.8% at Visit 3 in patients >55 years and from 47.7% to 16.5% in patients ≤55 years (p<0.0001).
The overall incidence of adverse events was low, leading to treatment discontinuation in only 3.0-3.6% of patients. Peripheral edema, a common adverse effect with calcium channel blockers in clinical practice, was reported by 2.7% of patients aged <65 years and by 4.6% of patients aged ≥65 years.
The efficacy and tolerability profiles of barnidipine as monotherapy or in combination with other antihypertensive drugs were shown to be favorable in both younger and older patients in a real-life practice setting. Randomized double-blind controlled studies are needed to confirm these results.
Hypertension has become increasingly prevalent in recent years due to increased longevity and other contributing life-style factors such as obesity, physical inactivity and an unhealthy diet [1-3]. Hypertension is a major risk factor for cardiovascular disease and it is well established that control of blood pressure (BP) reduces the risk of myocardial infarction and stroke [4, 5]. The 2013 joint guidelines of the European Society for Hypertension/European Society for Cardiology (ESH/ESC) suggest, along with a comprehensive approach to cardiovascular risk management, a target BP of <140/90 mmHg for patients with hypertension . BP control is however often poorly achieved in clinical practice [7-9]. Although monotherapy may sometimes suffice, mostly a combination of antihypertensive drugs from different classes is required to obtain good control [6, 10, 11].
According to the 2011 British Hypertension Society/National Institute of Clinical Excellence (NICE) guidelines for the clinical management of primary hypertension in adults , monotherapy with calcium channel blockers is indicated as a first-line treatment for patients aged 55 years or older with uncomplicated hypertension, unless such treatment is not suitable, for example because of edema or intolerance, or if there is evidence of heart failure or a high risk of heart failure [6, 11]. Calcium channel blockers either alone or in combination with other agent classes are also recommended by the 2013 joint guidelines of the ESH/ESC in low-to-moderate risk patients with uncomplicated hypertension  and are among the first choice options in the guidelines of the ESH/ESC and the U.S. eighth Joint National Committee (JNC 8) [6, 11].
Barnidipine is a long-acting and strong lipophilic dihydropyridine calcium channel blocker, with similar clinical efficacy to amlodipine and other calcium channel blockers [12-15] and is effective in combination with enalapril and losartan [16, 17]. Barnidipine has shown to be an effective antihypertensive agent in the management of hypertension in elderly patients [13, 18] and its efficacy is not negatively affected by age . The tolerability of barnidipine is considered to be generally good or excellent in most patients, including the elderly (≥75 years) [13, 18, 19]. Barnidipine has one of the lowest discontinuation rates in its drug class . The incidence of peripheral edema – one of the most common adverse events with calcium channel blockers especially in the elderly [22, 23] – is lower with barnidipine than with previous generation dihydropyridines [13, 20]. Other reported adverse events such as headache, flushing, vertigo and palpitations are mostly mild or moderate and transient in nature [13, 20] and are expected from its pharmacologic profile.
The tolerability and efficacy of barnidipine (10 or 20 mg) was studied in a large-scale open-label, prospective observational study in a population with essential hypertension, including patients with diabetic mellitus (n=20,279) (BASIC-HT; BArnidipine real-life Safety and tolerability In Chronic HyperTension) . The results confirmed the efficacy of barnidipine in the real-life setting of routine clinical practice as an effective treatment for BP reduction. The results also showed the good tolerability profile of barnidipine.
The overall results from the BASIC-HT study were reported in 2015 . The present paper describes the efficacy and tolerability of barnidipine monotherapy or combination treatment in elderly versus younger patients. These subgroup analyses by age were prespecified in the protocol and have not been reported elsewhere. Results were broken down in the age groups of patients aged ≤55 years and >55 years, as the age cut-off is of specific importance for BP target and for drug choice as a first-line treatment as per international guidelines [10, 11]. Frequencies of adverse events were broken down by the age groups of patients aged <65 years and ≥65 years, as patients with a chronological age of 65 years old or older are more likely to develop adverse events that are common with many calcium channel blockers, including edema and cardiac adverse events, such as tachycardia and/or palpitations [23, 25, 26].
2. MATERIALS AND METHODS
The BASIC-HT study was a post-marketing open-label, prospective, observational study conducted in routine practice in a large population in Belgium and Luxembourg. The full methodology of BASIC-HT was previously described . Eligible patients were those diagnosed with essential hypertension, including patients with diabetic mellitus, for whom barnidipine was considered to be a clinically appropriate treatment by the treating physician. The protocol was approved by an independent ethics committee [Clinical Research Ethical Committee (CREC) in Kortenberg, Belgium] and followed the Belgian code of deontology. Written informed consent was obtained from all patients before any study procedure was conducted.
Patients received barnidipine as monotherapy or in combination with other antihypertensive drug(s). Patients were prescribed barnidipine at the recommended dose of 10 mg orally once daily. If deemed necessary by the treating physician, a higher dose, i.e. 20 mg orally once daily, could be prescribed.
Efficacy was assessed from systolic BP (SBP) and diastolic BP (DBP) office recordings at baseline and at 2 additional routine visits, which took place during the 3-month follow-up period. At each visit, BP was measured on the same arm with a sphygmomanometer having a precision of 2 mmHg. Each measurement was repeated 3 times and the mean value of these measurements was used in the analyses. Pulse pressure was calculated as the difference between SBP and DBP.
Tolerability was assessed from the frequency and severity of adverse events and by recording of heart rates (HR). HR was recorded at the beginning and at the end of each visit and was measured in beats/min (bpm).
At each visit, the treating physician checked if any adverse event had occurred since the last visit. For each adverse event, a structured questionnaire was completed by the treating physician with a separate questionnaire for serious adverse events. Dropout rates were used to indirectly assess adherence to treatment. Treatment satisfaction was evaluated by the investigator based on the tolerability and efficacy after 3 months of therapy.
2.2. Statistical Analysis
The statistical analysis was performed using SAS software for WINDOWS version 9.2. Descriptive statistics of SBP, DBP, pulse pressure and HR at each visit were calculated for quantitative variables and consisted of the number of available and missing observations, mean, standard deviation (SD), minimum, maximum, median, and 95% confidence intervals (CIs). Frequency distributions were provided for ordinal and nominal variables and consisted of the numbers and percentages for each score or group.
BP and HR data were assessed in the subgroups of patients aged ≤55 years versus patients aged >55 years.
Adverse events were coded using the Medical Dictionary for Regulatory Activities (MedDRA) version 12.0. The frequencies of adverse events for younger (<65 years) and elderly patients (≥65 years) were compared using descriptive statistics.
3.1. Demographics and Other Baseline Characteristics
A total of 20,275 out of the 20,479 enrolled patients were included in the intent-to-treat (ITT) set, which comprised of all patients who were enrolled and treated, and for whom follow-up information was available. Subgroup analyses by age were performed on all patients from the ITT set for whom age was reported (n=19,558 in total; i.e., 10,313 patients <65 years and 9,245 patients ≥65 years).
Most patients were aged >55 years (n=14,023; 71.7%), with a mean age of 69.3 years (Table 1). Approximately one-quarter of all patients (n=4,778; 24.4%) were aged between 55-64 years, and about half of the patients were aged ≥65 years (n=9,245; 47.3%) of which 3,597 patients (18.4%) were older than 75 years (data not shown).
|–||–||≤55 years||>55 years|
|Age (years)||n (%)||5,535||(28.3%)||14,023||(71.7%)|
|Body mass index (kg/m2)||n||5,418||13,684|
|SD: Standard deviation|
The mean age of the patients aged ≤55 years (n=5,535; 28.3%) was 47.6 years. Although there were approximately equal numbers of males and females in the study, the younger age group comprised of more males (59%) than females (41%) while the older age group included more females (53%) than males (47%).
The mean body mass index (BMI) was comparable in both age groups. Older patients more often had diabetes than younger patients (18.7 vs 10.9%).
Barnidipine was more often prescribed as monotherapy in younger (63.4%) than in older patients (42.7%) (Table 2). In contrast, barnidipine in combination with other antihypertensive drug(s) was prescribed more often in older (57.3%) than in younger patients (36.6%).
|–||–||≤55 years||>55 years|
|Monotherapy||n (%)||2,322 (63.4%)||3,985 (42.7%)|
|Combination with other antihypertensive drug(s)||n (%)||1,341 (36.6%)||5,343 (57.3%)|
The start dose of barnidipine was 10 mg in the vast majority of patients, with no clinically relevant difference between age groups (n=5,132 patients ≤55 years; 93.3%; and n=12,772 patients >55 years; 91.7%). The remaining patients received a start dose of 20 mg (n=369; 6.7% and n=1,158; 8.3%, respectively). The percentages of patients in these dosage groups were calculated with the total number of patients for whom the age and also the dosage were reported (n=19,431 in total; n=5,501 younger and n=13,930 older patients).
The mean SBP and DBP values at baseline were 158.2/94.9 mmHg and 160.2/92.2 mmHg for the younger and older age group respectively, and were well above the target value of <140/90 mmHg , with no clinically meaningful differences between age groups (Table 3).
The mean pulse pressure, however, was higher in patients >55 years compared with younger patients (68.1 and 63.3 mmHg, respectively; p<0.001), and more patients >55 years had a pulse pressure >60 mmHg at baseline (61.1% compared with 47.7% of patients aged ≤55 years).
The mean HR value at the end of the baseline visit in the 10 mg barnidipine dosage group was 75.5 bpm for patients aged ≤55 years and 74.2 for patients aged >55 years (95% confidence interval for group difference 0.98 < 1.27 <1.57; p<0.001).
3.2. Efficacy Analysis
There was a statistically significant and clinically meaningful decrease in mean SBP and mean DBP in both younger and older patients (aged >55 and ≤55 years, respectively) treated with barnidipine over the course of the 3-month follow-up period (p<0.0001), with no notable clinical differences between age groups (Table 3). The mean SBP and DBP values at the end of the 3-month follow-up period were below the blood pressure target of <140/90 mmHg for individual patients.
|–||–||–||≤55 years||>55 years|
|Pressure (mmHg)||mean (SD)||158.2 (13.9)||160.2 (14.9)|
|95% CI||157.8; 158.6||160.0; 160.5|
|mean (SD)||142.7 (12.6)||144.2 (12.8)|
|95% CI||142.3; 143.0||144.0; 144.4|
|Change from baseline||-15.5 (p<0.0001)||-16.0 (p<0.0001)|
|mean (SD)||137.1 (11.3)||138.6 (11.3)|
|95% CI||136.8; 137.4||138.4; 138.8|
|Change from baseline||-21.1 (p<0.0001)||-21.6 (p<0.0001)|
|Pressure (mmHg)||mean (SD)||94.9 (9.0)||92.2 (9.2)|
|95% CI||94.6; 95.1||92.0; 92.3|
|mean (SD)||85.9 (8.2)||84.3 (7.9)|
|95% CI||85.6; 86.1||84.2; 84.4|
|Change from baseline||-9.0 (p<0.0001)||-7.9 (p<0.0001)|
|mean (SD)||82.5 (7.2)||81.3 (6.9)|
|95% CI||82.3; 82.7||81.2; 81.5|
|Change from baseline||-12.4 (p<0.0001)||-10.9 (p<0.0001)|
|(mmHg)||mean (SD)||63.3 (13.8)||68.1 (14.9)|
|95% CI||63.0; 63.7||67.8; 68.3|
|mean (SD)||56.8 (11.6)||59.9 (12.0)|
|95% CI||56.5; 57.1||59.7; 60.1|
|Change from baseline||-6.5 (p<0.0001)||-8.2 (p<0.0001)|
|mean (SD)||54.6 (10.3)||57.3 (10.9)|
|95% CI||54.3; 54.9||57.1; 57.5|
|Change from baseline||-8.7 (p<0.0001)||-10.8 (p<0.0001)|
95% CIs which do not overlap between groups are in bold; SD: Standard deviation; CI: confidence interval;
p-values for change from baseline calculated with Student's t-test
The mean change in SBP in older (>55 years) and younger (≤55 years) patients at Visit 2 was -16.0 mmHg and -15.5 mmHg, respectively, and the mean change in DBP was -7.9 mmHg and -9.0 mmHg, respectively (Fig. 1).
|Fig. 1. Mean systolic blood pressure (SBP) and diastolic blood pressure (DBP) at each visit for patients treated with barnidipine as monotherapy or in combination, split by age.|
A further decrease in SBP and DBP was observed at Visit 3, with a mean change from baseline of -21.6 mmHg and -21.1 mmHg, respectively for SBP, and a mean change from baseline of -10.9 mmHg and -12.4 mmHg, respectively, for DBP.
The decrease in mean pulse pressure after approximately 3 months of barnidipine therapy was larger in patients >55 years (-10.8 mmHg) compared with patients ≤55 years (-8.7 mmHg; p<0.0001). This trend was already visible at Visit 2 (-8.2 mmHg and -6.5 mmHg, respectively; p<0.0001).
3.3. Pulse Pressure
The proportion of patients with pulse pressure >60 mmHg decreased over the course of the 3-month follow-up period from 61.1% at baseline to 24.8% at Visit 3 in patients >55 years and from 47.7% to 16.5% in patients ≤55 years (Fig. 2). The difference was considered clinically meaningful as elevated pulse pressure >60 mmHg is an established marker of adverse outcome in elderly patients with hypertension [27-29].
|Fig. 2. Mean pulse pressure at each visit for patients treated with barnidipine as monotherapy or in combination, split by age.|
3.4. Heart Rate
The mean HR tended to decrease over the 3-month follow-up period for both older (>55 years) and younger patients (≤55 years) and for both dosage groups (10 mg and 20 mg). Overall, the decrease tended to be somewhat larger in younger patients than in older patients, and also somewhat larger with the 20 mg dosage than with the 10 mg dosage.
Younger patients who received a dose of 10 mg barnidipine had a change of -2.2 bpm (95% CI -2.0; -2.4) in HR whereas patients >55 years showed a mean change of -1.4 bpm (95% CI -1.30; -1.6). The difference was statistically significant (p<0.001).
Similarly, the mean reduction in HR in the age group of patients ≤55 years who received barnidipine 20 mg was -3.1 bpm (95% CI -2.3; -3.9) whereas the mean HR reduction in the older age group (>55 years) was -2.0 bpm (95% CI -1.5; -2,5, and p=0.074).
It should however be noted that baseline values in the age group of patients ≤55 years were higher than in patients >55 years, thereby leaving more room for improvement. Also, despite the smaller decrease from baseline, patients >55 years still had better (lower) mean HR values at the end of Visit 3 compared with patients ≤55 years.
3.5. Adverse Events
Barnidipine was well tolerated. The incidence of adverse events was low and generally comparable among age groups (Table 4). Peripheral edema was the most commonly reported adverse event, and was observed in 2.7% of patients aged <65 years and in 4.6% of patients aged ≥65 years. Headache was reported in 1.8% of patients aged <65 years and in 1.4% of patients aged ≥65 years.
|–||<65 years (n=10,313)||≥65 years (n=9,245)|
|Adverse Event||Number of Patients (%)||Number of Patients (%)|
|Edema peripheral||281 (2.7%)||426 (4.6%)|
|Headache||190 (1.8%)||130 (1.4%)|
|Flushing||94 (0.9%)||63 (0.7%)|
|Dizziness||64 (0.6%)||56 (0.6%)|
|Palpitations||50 (0.5%)||26 (0.3%)|
|Hot flush||43 (0.4%)||24 (0.3%)|
|Nausea||38 (0.4%)||52 (0.6%)|
|Erythema||30 (0.3%)||21 (0.2%)|
|Edema||21 (0.2%)||51 (0.6%)|
|Tachycardia||17 (0.2%)||21 (0.2%)|
|Fatigue||10 (0.1%)||11 (0.1%)|
|Malaise||6 (0.1%)||11 (0.1%)|
The incidence of vascular adverse events (flushing, hot flush) and cardiac adverse events (tachycardia, palpitations) was low (<1.0%) with no notable or clinically meaningful differences between age groups.
3.6. Dropout Rate
The vast majority of patients completed the 3-month follow-up period. The dropout rate was low, i.e. 447 (8.6%) patients aged ≤55 years and 989 (7.5%) patients aged >55 years, discontinued treatment at any time during the study. The dropout rates due to adverse events were 3.0% (168 out of 5,535) and 3.6% (501 of 18,642), respectively. Over 95% of patients intended to continue the barnidipine treatment after the end of the study.
3.7. Treatment Satisfaction
Efficacy was considered very good or good for approximately 93% of younger and older patients receiving barnidipine monotherapy and for approximately 90% of the patients receiving barnidipine in combination with other antihypertensive drugs (Table 5).
|–||≤55 years||>55 years||≤55 years||>55 years|
|Efficacy, n (%)|
|Tolerance n (%)|
Likewise, the tolerability of barnidipine was very good or good in over 92% of patients, with no relevant differences between age groups.
Hypertension is a major risk factor for the development of cardiovascular disease, and unlike other risk factors such as race or family history, can be controlled, treated or modified. As BP tends to rise with age, BP control in the elderly may significantly contribute to reduced mortality and morbidity in this age group [6, 10, 11].
With advanced age, systolic hypertension becomes predominant, which is largely accounted for by loss of elasticity and increasing rigidity of large arteries. Also, in elderly patients, the activity of the renin-angiotensin system is generally suppressed, and as a consequence BP reduction with an angiotensin converting enzyme (ACE) inhibitor or an angiotensin II receptor blocker may be small [30, 31]. Therefore, calcium channel blockers are the preferred first-line treatment for patients aged 55 years or older as monotherapy (according to the NICE guidelines)  or among the first choice options in the guidelines of the ESH/ESC  and the JNC 8 .
If more than one drug is needed, combination therapy with a calcium channel blocker and either an ACE inhibitor or an angiotensin II receptor blocker is recommended. This combination has been proven superior to other combinations (e.g. a β-blocker plus a diuretic, or an ACE inhibitor/angiotensin II receptor blocker plus a diuretic) in patients of all ages, as it shows a lower incidence of cardiovascular events and adverse events, while it has similar effects in lowering BP and preserving renal function [32-34]. In keeping with these results, Falaschetti et al. reported that BP management and control between 1994 and 2011 in England improved when the most commonly prescribed combination therapies changed from diuretics plus β-blockers to renin-angiotensin system blockers plus diuretics in 2006, and to renin-angiotensin system blockers plus calcium channel blockers in 2011 . Awareness, treatment, and control rates progressively improved across each stage of this 17-year period, with the prevalence of control across all treated patients almost doubling from 33% in 1994 to 63% in 2011. Nevertheless, of all adults in 2011, hypertension was controlled in only 37% . Similar percentages (i.e. 22-42% for men, and 27-39% for women, depending on age) were recently reported for BP control in treated patients in high-income countries . Therefore, hypertension awareness and appropriate treatment schemes, that avoid therapeutic inertia and enhance adherence, must continuously be the main focus.
Barnidipine is a strong lipophilic calcium channel blocker with efficacy similar to other dihydropyridines [12, 13]. The tolerability and efficacy of barnidipine (10 or 20 mg) given alone or in combination with one or more other antihypertensive drugs was recently studied in the real-life setting of routine clinical practice. Over 20,000 patients with hypertension were enrolled in the BASIC-HT study . The overall results from this open-label prospective observational study showed that barnidipine is an effective treatment for BP reduction, comparable to the results obtained from randomized studies [13, 24]. The results also confirmed the good tolerability profile of barnidipine in a real life setting. The present paper describes for the first time the results from the subgroup analysis by age that was prespecified in the protocol and has not been reported elsewhere. Most patients (71.7%) in the BASIC-HT study were aged >55 years. Approximately one-quarter of all patients (24.4%) were aged between 55-64 years, about half of the patients were aged ≥65 years (47.3%), and 18.4% of patients were older than 75 years. The age cut-offs that were used for the subgroup analyses (≤55 vs >55 years and <65 vs ≥65 years) were based on several current international hypertension guidelines that have dichotomized age groups around a cut-off value of 55-60 years for choice of first-line treatment [6, 11] and on literature data that suggest that elderly patients (i.e. those with a chronological age of 65 years old or older) are more likely to develop adverse events that are common with many calcium channel blockers [23, 25, 26].
The subgroup analysis by age showed a statistically significant and clinically meaningful decrease in mean SBP and DBP in both younger and older patients over the course of the 3-month follow-up period. The mean SBP and DBP values at the end of the 3-month follow-up period were below the BP target of <140/90 mmHg for individual patients, i.e. 137.1/82.5 mmHg for patients ≤55 years, and 138.6/81.3 mmHg for patients >55 years. The results of the SPRINT study  showed that a further reduction (i.e. a lower SBP target of <120 mmHg; in an unattended automated office BP measurement protocol, so rather compared with <135 mmHg SBP ) reduced the rates of fatal and nonfatal major cardiovascular events and death from any cause in a patient population of ≥50 years to a larger extent compared to a SBP target of <140 mmHg . However, in the SPRINT study, a more intensive BP management regimen was associated with higher rates of serious adverse events of hypotension, syncope, electrolyte abnormalities, and acute kidney injury or failure . Such an intensified approach may therefore be not safe enough for treatment of elderly, more fragile patients with co-morbidities. In a prespecified subgroup of elderly aged 75 years or older in the SPRINT study, the beneficial results of lower BP targets were confirmed, but the frail elderly remain a risk group .
In older patients with hypertension, pulse pressure appears to be a major determinant of cardiovascular risk related to arterial stiffness. Elevated pulse pressure (above 60 mmHg) in the elderly is a risk factor for asymptomatic organ damage [27-29]. In the present BASIC-HT study, a reduction in pulse pressure was observed after 1 and 3 months of barnidipine treatment. The reduction from baseline was larger in patients older than 55 years (-10.8 mmHg) compared with younger patients (-8.7 mmHg). Moreover, after approximately 3 months of treatment, only 24.8% of the older patients still presented with a pulse pressure of >60 mmHg, compared with 61.1% of patients at baseline. This is in line with an earlier study with barnidipine, in which the pulse pressure was significantly lowered to a mean of 58 mmHg after 6 months of treatment .
Various studies have reported a negative association between elevated resting HR and cardiovascular outcomes in hypertension, coronary artery disease and heart failure [40-42]. The mean resting HR in the present BASIC-HT study tended to decrease slightly with treatment duration for both older and younger patients. These results are in line with the results from earlier studies with barnidipine [38, 43] and supports the idea that barnidipine does not cause reflex neurohumoral activation .
Barnidipine was well tolerated. The incidence of adverse events was low and generally comparable among age groups, and less than 4% of patients dropped out due to adverse events. Events reported with the highest incidence (peripheral edema, headache, nausea, dizziness and flushing) are events generally reported in patients treated with calcium channel blockers and caused by drug-induced vasodilation.
Peripheral edema is one of the most common adverse effects with dihydropyridine calcium channel blockers in clinical practice and is likely to be related to the vasodilatory action of these drugs [22, 44, 45]. The incidence rates for peripheral edema reported in the literature range from 3-30%, partly also because the effect may be more common in women [23, 26, 45] and also varies (among others) with age [19, 25] and the type and dose of the calcium channel blocker [22, 23, 45-47]. While calcium channel blocker-associated edema is not life-threatening, it is distressing to many patients, and may contribute to an increased dropout rate and decreased compliance with therapy  or can even effectively deter a clinician from prescribing these drugs . The incidence of peripheral edema with barnidipine in the BASIC-HT study was low (i.e. observed in only 4.6% of patients aged 65 years or older) and comparable with that observed in randomized clinical studies including elderly and very elderly hypertensive patients [19, 20]. It has been hypothesized that this low incidence may be due to the slow onset of action of barnidipine and the fact that it has higher affinity for smooth muscles in the mesenteric and renal tissue vascular beds than for peripheral arteries in the extremities [12, 48]. The low incidence as observed in the present BASIC-HT study may also partly be due to the fact that more than half (54.1%) of the patients older than 55 years of age in were prescribed barnidipine in combination with another antihypertensive therapy. If these were combinations with an ACE inhibitor or with an angiotensin receptor blocker, as recommended in current international hypertension guidelines, the incidence rates of calcium channel blocker-related adverse events would be typically reduced compared with monotherapy [22, 46, 49]. The other hypertensive drugs that were prescribed in combination therapy with barnidipine in the present BASIC-HT study were however not further specified, so no distinct conclusions can be drawn.
Cardiac side effects such as tachycardia and/or palpitations are common with dihydropyridine calcium channel blockers in general. In the present BASIC-HT study, the incidence of cardiac adverse events was very low (≤0.5%) with no notable or clinically meaningful differences between older and younger patients. This is in line with previous studies with barnidipine, and is expected from its pharmacologic profile [12, 13].
Efficacy and tolerability were considered by the investigator to be very good or good in over 92% of patients.
In summary, the results from the present analysis show that barnidipine monotherapy or when given in combination with antihypertensive drugs from other drug classes can safely and effectively be used for treatment of patients with uncomplicated mild to moderate hypertension, including the elderly population. The mean SBP and DBP values at the end of the 3-month follow-up period were below the BP target of <140/90 mmHg for individual patients. Barnidipine monotherapy or as part of combination therapy was well tolerated. The incidence of peripheral edema, one of the most common adverse effects with dihydropyridine calcium channel blockers and often the cause of treatment discontinuation, was low in both age groups. Based on the results of the present study, the risk-benefit profile of barnidipine is considered favorable in both younger and older patients. Additional randomized double-blind controlled studies are needed to confirm these results.
The efficacy and tolerability profiles of barnidipine as monotherapy or in combination with other antihypertensive drugs in keeping with current international treatment guidelines were shown to be similar in younger and older patients with hypertension in a real-life practice setting. Barnidipine can therefore be effectively and safely used in patients of all ages, including elderly patients. The low incidences of peripheral edema, palpitations and tachycardia, suggest a role of barnidipine as antihypertensive drug for patients not tolerating other calcium channel blockers and patients at greater cardiovascular risk.
ETHICS APPROVAL AND CONSENT TO PARTICIPATE
The protocol was approved by an independent ethics committee [Clinical Research Ethical Committee (CREC) in Kortenberg, Belgium] and followed the Belgian code of deontology. Written informed consent was obtained from all patients before any study procedure was conducted.
HUMAN AND ANIMAL RIGHTS
No animals were used in this research. All research procedures followed were in accordance with the ethical standards of the committee responsible for human experimentation (institutional and national), and with the Helsinki Declaration of 1975, as revised in 2008 (http://www.wma.net/en/20activities/10ethics/10helsinki/.
CONSENT FOR PUBLICATION
CONFLICT OF INTEREST
The study was sponsored by Fournier Pharma SA. The manuscript was sponsored by Astellas Pharma B.V. Robert Lins received consulting fees from Astellas Pharma B.V. for revising the original set-up of the protocol, EC submission, revising the original results, interpreting the data and revising the article. Caroline de Vries is an employee of Astellas Pharma B.V. The authors did not have other actual or potential competing financial interests.
We would like to thank AUTHOR! (Netherlands) for medical writing assistance and DICE NV (Belgium) for the statistical analyses.
|||Cooper-DeHoff RM, Pepine CJ. Metabolic syndrome and cardiovascular disease: Challenges and opportunities. Clin Cardiol 2007; 30(12): 593-7.
|||Hayden MR, Sowers JR. Treating hypertension while protecting the vulnerable islet in the cardiometabolic syndrome. J Am Soc Hypertens 2008; 2(4): 239-66.
|||Velagaleti RS, Vasan RS. Heart failure in the twenty-first century: Is it a coronary artery disease or hypertension problem? Cardiol Clin 2007; 25(4): 487-495, v.
|||Law MR, Morris JK, Wald NJ. Use of blood pressure lowering drugs in the prevention of cardiovascular disease: Meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ 2009; 338: b1665.
|||Moran AE, Odden MC, Thanataveerat A, et al. Cost-effectiveness of hypertension therapy according to 2014 guidelines. N Engl J Med 2015; 372(5): 447-55.
|||Mancia G, Fagard R, Narkiewicz K, et al. 2013 ESH/ESC Guidelines for the management of arterial hypertension: The Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens 2013; 31(7): 1281-357.
|||Kotseva K, Wood D, De Bacquer D, et al. EUROASPIRE IV: A European Society of Cardiology survey on the lifestyle, risk factor and therapeutic management of coronary patients from 24 European countries. Eur J Prev Cardiol 2016; 23(6): 636-48.
|||Wolf-Maier K, Cooper RS, Banegas JR, et al. Hypertension prevalence and blood pressure levels in 6 European countries, Canada, and the United States. JAMA 2003; 289(18): 2363-9.
|||Yang F, Qian D, Hu D. Prevalence, awareness, treatment, and control of hypertension in the older population: Results from the multiple national studies on ageing. J Am Soc Hypertens 2016; 10(2): 140-8.
|||National Clinical Guideline Centre Hypertension: The clinical management of primary hypertension in adults Clinical Guideline 127 Methods, evidence, and recommendations Commissioned by the National Institute for Health and Clinical Excellence 2011. Available at: https://www.nice.org.uk/guidance/cg127|
|||James PA, Oparil S, Carter BL, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: Report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA 2014; 311(5): 507-20.
|||van Zwieten PA. The pharmacological properties of lipophilic calcium antagonists. Blood Press Suppl 1998; 2: 5-9.
|||Malhotra HS, Plosker GL. Barnidipine. Drugs 2001; 61(7): 989-96.
|||Spieker C. Efficacy and tolerability of once-daily barnidipine in the clinical management of patients with mild to moderate essential hypertension. Blood Press Suppl 1998; 1: 15-21.
|||Argenziano L, Izzo R, Iovino G, et al. Distinct vasodilation, without reflex neurohormonal activation, induced by barnidipine in hypertensive patients. Blood Press Suppl 1998; 1: 9-14.
|||Ruilope LM, Coca A. The role of combination therapy in the treatment of hypertension. Blood Press Suppl 1998; 1: 22-6.
|||Parati G, Giglio A, Lonati L, et al. Effectiveness of barnidipine 10 or 20 mg plus losartan 50-mg combination versus losartan 100-mg monotherapy in patients with essential hypertension not controlled by losartan 50-mg monotherapy: A 12-week, multicenter, randomized, open-label, parallel-group study. Clin Ther 2010; 32(7): 1270-84.
|||Naber FB, Häge R, Mortelmans J. Barnidipine monotherapy and combination therapy in older patients with essential hypertension: A long-term study. Int J Clin Pract Suppl 2000; 114(114): 27-35.
|||Otterstad JE, Ruilope LM. Treatment of hypertension in the very old. Int J Clin Pract Suppl 2000; 114(114): 10-9.
|||van der Velden JW, Beudeker HJ, Nishi M. Diversity and intensity of adverse events in the treatment of hypertension with barnidipine. Blood Press Suppl 1998; 1: 27-9.
|||Mancia G, Parodi A, Merlino L, Corrao G. Heterogeneity in antihypertensive treatment discontinuation between drugs belonging to the same class. J Hypertens 2011; 29(5): 1012-8.
|||Fogari R, Zoppi A, Derosa G, et al. Effect of valsartan addition to amlodipine on ankle oedema and subcutaneous tissue pressure in hypertensive patients. J Hum Hypertens 2007; 21(3): 220-4.
|||Messerli FH. Vasodilatory edema: A common side effect of antihypertensive therapy. Curr Cardiol Rep 2002; 4(6): 479-82.
|||Lins R, Marckx P, Vandebeek R, Vanhoutvinck C, Neuville O. Barnidipine real-life tolerability in arterial hypertension: Results from the BASIC-HT study. Acta Clin Belg 2015; 70(4): 244-50.
|||Fogari R, Malamani GD, Zoppi A, et al. Comparative effect of lercanidipine and nifedipine gastrointestinal therapeutic system on ankle volume and subcutaneous interstitial pressure in hypertensive patients: A double-blind, randomized, parallel-group study. Curr Ther Res 2000; 61: 850-62.
|||Sica D. Calcium channel blocker-related periperal edema: Can it be resolved? J Clin Hypertens (Greenwich) 2003; 5(4): 291-4.
|||Benetos A, Safar M, Rudnichi A, et al. Pulse pressure: A predictor of long-term cardiovascular mortality in a French male population. Hypertension 1997; 30(6): 1410-5.
|||Blacher J, Staessen JA, Girerd X, et al. Pulse pressure not mean pressure determines cardiovascular risk in older hypertensive patients. Arch Intern Med 2000; 160(8): 1085-9.
|||Briet M, Boutouyrie P, Laurent S, London GM. Arterial stiffness and pulse pressure in CKD and ESRD. Kidney Int 2012; 82(4): 388-400.
|||Dickerson JE, Hingorani AD, Ashby MJ, Palmer CR, Brown MJ. Optimisation of antihypertensive treatment by crossover rotation of four major classes. Lancet 1999; 353(9169): 2008-13.
|||Materson BJ, Reda DJ, Cushman WC. Department of veterans Affairs single-drug therapy of hypertension study. Revised figures and new data. Am J Hypertens 1995; 8(2): 189-92.
|||Chi C, Tai C, Bai B, et al. Angiotensin system blockade combined with calcium channel blockers is superior to other combinations in cardiovascular protection with similar blood pressure reduction: A meta-analysis in 20,451 hypertensive patients. J Clin Hypertens (Greenwich) 2016; 18(8): 801-8.
|||Dahlöf B, Sever PS, Poulter NR, et al. Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA): A multicentre randomised controlled trial. Lancet 2005; 366(9489): 895-906.
|||Jamerson K, Weber MA, Bakris GL, et al. Benazepril plus amlodipine or hydrochlorothiazide for hypertension in high-risk patients. N Engl J Med 2008; 359(23): 2417-28.
|||Falaschetti E, Mindell J, Knott C, Poulter N. Hypertension management in England: A serial cross-sectional study from 1994 to 2011. Lancet 2014; 383(9932): 1912-9.
|||Wright JT Jr, Williamson JD, Whelton PK, et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med 2015; 373(22): 2103-16.
|||Kjeldsen SE, Lund-Johansen P, Nilsson PM, Mancia G. Unattended blood pressure measurements in the systolic blood pressure intervention trial. Hypertension 2016; 67(5): 808-12.
|||Williamson JD, Supiano MA, Applegate WB, et al. Intensive vs standard blood pressure control and cardiovascular disease outcomes in adults aged ≥75 Years: A randomized clinical trial. JAMA 2016; 315(24): 2673-82.
|||Palombo C, Malshi E, Morizzo C, et al. Arterial wave reflection during antihypertensive therapy with barnidipine: A 6-month, open-label study using an integrated cardiovascular ultrasound approach in patients with newly diagnosed hypertension. Clin Ther 2009; 31(12): 2873-85.
|||Fox K, Ford I, Steg PG, Tendera M, Robertson M, Ferrari R. Heart rate as a prognostic risk factor in patients with coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): A subgroup analysis of a randomised controlled trial. Lancet 2008; 372(9641): 817-21.
|||Kolloch R, Legler UF, Champion A, et al. Impact of resting heart rate on outcomes in hypertensive patients with coronary artery disease: Findings from the INternational VErapamil-SR/trandolapril STudy (INVEST). Eur Heart J 2008; 29(10): 1327-34.
|||Böhm M, Swedberg K, Komajda M, et al. Heart rate as a risk factor in chronic heart failure (SHIFT): The association between heart rate and outcomes in a randomised placebo-controlled trial. Lancet 2010; 376(9744): 886-94.
|||Rossetti G, Pizzocri S, Brasca F, et al. Antihypertensive effect of barnidipine 10 mg or amlodipine 5 to 10 mg once daily in treatment-naive patients with essential hypertension: A 24-week, randomized, open-label, pilot study. Curr Ther Res Clin Exp 2008; 69(3): 192-206.
|||Pedrinelli R, Dell’Omo G, Mariani M. Calcium channel blockers, postural vasoconstriction and dependent oedema in essential hypertension. J Hum Hypertens 2001; 15(7): 455-61.
|||Weir MR. Incidence of pedal edema formation with dihydropyridine calcium channel blockers: Issues and practical significance. J Clin Hypertens (Greenwich) 2003; 5(5): 330-5.
|||Brown MJ, Palmer CR, Castaigne A, et al. Morbidity and mortality in patients randomised to double-blind treatment with a long-acting calcium-channel blocker or diuretic in the International Nifedipine GITS study: Intervention as a Goal in Hypertension Treatment (INSIGHT). Lancet 2000; 356(9227): 366-72.
|||Jamerson KA, Nwose O, Jean-Louis L, Schofield L, Purkayastha D, Baron M. Initial angiotensin-converting enzyme inhibitor/calcium channel blocker combination therapy achieves superior blood pressure control compared with calcium channel blocker monotherapy in patients with stage 2 hypertension. Am J Hypertens 2004; 17(6): 495-501.
|||Janssen BJ, Kam KL, Smits JF. Preferential renal and mesenteric vasodilation induced by barnidipine and amlodipine in spontaneously hypertensive rats. Naunyn Schmiedebergs Arch Pharmacol 2001; 364(5): 414-21.
|||Makani H, Bangalore S, Romero J, Wever-Pinzon O, Messerli FH. Effect of renin-angiotensin system blockade on calcium channel blocker-associated peripheral edema. Am J Med 2011; 124(2): 128-35.