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The Valsartan Antihypertensive Long-term Use Evaluation (VALUE) trial of cardiovascular events in hypertension.
Insights
Essential hypertension affects many, with poor blood pressure control. The VALUE trial compared valsartan and amlodipine to reduce cardiovascular events in high-risk patients.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Essential hypertension is a significant public health concern, with suboptimal blood pressure control in a majority of treated patients.
- Despite proven benefits of treatment, cardiovascular morbidity and mortality rates remain high, necessitating drugs that not only control blood pressure but also reduce cardiovascular events.
- Angiotensin II plays a critical role in hypertension-related complications, including left ventricular hypertrophy, vascular hypertrophy, endothelial dysfunction, and heart failure.
Purpose of the Study:
- To evaluate whether valsartan, an angiotensin II antagonist, is more effective than amlodipine, a calcium channel blocker, in reducing cardiovascular mortality and morbidity in patients with essential hypertension.
- To assess the efficacy of valsartan versus amlodipine for an equivalent blood pressure reduction.
Main Methods:
- The Valsartan Antihypertensive Long-term Use Evaluation (VALUE) trial is a prospective, multinational, double-blind, randomized, active-controlled study.
- It involves 14,400 hypertensive patients aged 50 years or older with high cardiovascular risk, followed for 4 years or until 1450 primary endpoints occur.
- Patients were randomized to receive either valsartan or amlodipine with a response-dependent dose titration scheme.
Main Results:
- The VALUE trial is designed to compare the long-term effects of valsartan and amlodipine on cardiovascular outcomes.
- It aims to determine if targeting the renin-angiotensin system with valsartan offers superior protection against cardiovascular events compared to amlodipine in hypertensive patients.
- The study will also analyze the predictive power of a defined cardiovascular risk factor scale in a large hypertensive population.
Conclusions:
- The VALUE trial is uniquely positioned to provide critical data on the comparative effectiveness of an angiotensin II antagonist versus a calcium channel blocker in reducing cardiovascular events in high-risk hypertensive patients.
- Findings from VALUE are expected to inform clinical practice guidelines for hypertension management.
- The trial's design allows for robust assessment of cardiovascular risk stratification and the impact of different antihypertensive drug classes on patient outcomes.
Abstract:
Essential hypertension is a major Public Health issue. Although the number of treated hypertensive patients has increased, only 25% of treated patients have their blood pressure levels under control. The benefit of treating hypertension has been proven, but cardiovascular morbidity and mortality rates remain high. The ideal antihypertensive drug should not only normalize blood pressure levels, but also reduce the associated cardiovascular morbidity and mortality rates. The role of angiotensin II in systemic hypertension and its complications has been recently redefined. The potent trophic effects of angiotensin II on blood vessels and on cardiac cells have been well demonstrated, especially the role of angiotensin II in left ventricular hypertrophy, vascular hypertrophy, endothelial dysfunction, and congestive heart failure. Of all ongoing mortality and morbidity trials in systemic hypertension, VALUE (Valsartan Antihypertensive Long-term Use Evaluation) is the only one comparing an angiotensin II antagonist (valsartan) with a third-generation calcium channel blocker (amlodipine). The main hypothesis of the VALUE trial is that, for an equivalent decrease in blood pressure, valsartan will be more effective than amlodipine in decreasing cardiac mortality and morbidity. VALUE is a prospective, multinational, multicentre, double-blind, randomized, active-controlled, 2-arm parallel group comparison with a response-dependent dose titration scheme. VALUE involves 14,400 patients in over 30 countries, who will be followed for 4 years or until 1450 patients experience a primary endpoint. The population to be included in VALUE consists of hypertensive men and women, aged 50 years or older, and at a relatively high risk of sustaining a cardiovascular event. The high risk profile is defined taking into account age, gender, and a list of cardiovascular risk factors and disease factors. Risk factors are cigarette smoking, hypercholesterolaemia, diabetes mellitus, uncomplicated left ventricular hypertrophy, proteinuria, and high serum creatinine. Disease factors include documented history of myocardial infarction, peripheral vascular disease, stroke or transient ischaemic attack, or the presence of left ventricular hypertrophy with strain on the ECG. A unique feature of VALUE is the assessment of the predictive power of this cardiovascular risk factor scale in a large population of treated hypertensive patients. The trial started on 10 September 1997.
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