Angiotensin receptor blockers versus angiotensin-converting enzyme inhibitors: where do we stand now?

Michael Böhm1

  • 1Department of Internal Medicine III, Cardiology/Angiology and Intensive Cardiac Medicine, University of Saarland, Homburg/Saar, Germany. michael.boehm@uniklinikum-saarland.de

Insights

Renin-angiotensin-aldosterone system (RAAS) blockade using ACE inhibitors or ARBs benefits cardiovascular health across all disease stages. Ongoing trials will further clarify the advantages of RAAS blockade in high-risk patients.

Area of Science:

  • Cardiology
  • Pharmacology
  • Nephrology

Background:

  • Cardiovascular disease progresses from risk factors like hypertension to atherosclerosis, organ damage, heart failure, and stroke.
  • Renin-angiotensin-aldosterone system (RAAS) blockade, via ACE inhibitors or ARBs, offers benefits throughout this continuum.
  • ACE inhibitors have demonstrated cardiovascular event reduction, but ARB data is limited in this area.

Purpose of the Study:

  • To review the established benefits of RAAS blockade in cardiovascular disease.
  • To highlight the need for further research on ARBs and RAAS blockade across the cardiorenovascular continuum.
  • To introduce insights from trials like ONTARGET and TRANSCEND.

Main Methods:

  • Review of existing clinical trial data on ACE inhibitors and ARBs.
  • Focus on studies examining effects on atherosclerosis, endothelial function, and target organ damage.
  • Analysis of data from high-risk patient populations in trials like ONTARGET and TRANSCEND.

Main Results:

  • Both ACE inhibitors and ARBs mitigate endothelial dysfunction and atherosclerosis.
  • ACE inhibitors reduce cardiovascular events in coronary artery disease patients.
  • Both drug classes protect organs like the heart and kidneys and reduce mortality/morbidity in heart failure.

Conclusions:

  • RAAS blockade is beneficial across the cardiovascular disease continuum.
  • Further insights into ARB benefits and RAAS blockade are expected from ongoing trials.
  • These trials will clarify the role of telmisartan and ramipril in high-risk patients with end-organ damage.

Related Concept Videos

Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors01:30

Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors

Angiotensin-converting enzyme (ACE), a vital component of the renin-angiotensin-aldosterone system, is abundant in lung endothelial cells. ACE converts the inactive decapeptide, angiotensin I, into the active octapeptide, angiotensin II. This potent vasoconstrictor narrows blood vessels, increasing resistance to blood flow and elevating blood pressure. Angiotensin II also stimulates aldosterone production, encouraging kidney cells to reabsorb more sodium and water from urine, thereby increasing...
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
Antihypertensive Drugs: Angiotensin II Receptor Blockers01:30

Antihypertensive Drugs: Angiotensin II Receptor Blockers

In the renin-angiotensin-aldosterone system, a hormone called angiotensin II plays a crucial role. It binds to the AT1 receptors in vascular smooth muscles coupled with Gq proteins. The activation of these receptors activates an enzyme called phospholipase C, which releases two molecules: inositol trisphosphate and diacylglycerol. These molecules cause a chain reaction that leads to the phosphorylation of myosin light chains and promotes interaction between actin and myosin, leading to smooth...
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme (ECE). Of...
Adrenergic Antagonists: Chemistry and Classification of β-Receptor Blockers01:25

Adrenergic Antagonists: Chemistry and Classification of β-Receptor Blockers

β-adrenergic antagonists, or β-blockers, modulate the sympathetic nervous system by targeting β-adrenoceptors and inhibiting catecholamine-mediated sympathetic responses. β-blockers differ in their adrenoceptor subtype affinity, lipophilicity, and α-blocking capabilities. The history of β-blocker development began with the prototype, dichloroisoprenaline, which exhibited partial agonist activity. As a result, propranolol was developed as a pure antagonist but nonselective agent, paving the way...