Comparative effectiveness of renin-angiotensin system inhibitors in hypertension

C Michael White1

  • 1University of Connecticut School of Pharmacy, 80 Seymour Street, Hartford, CT 06102-5037, USA. cmwhite@harthosp.org.

Insights

For hypertension, angiotensin receptor blockers (ARBs) and angiotensin-converting enzyme inhibitors (ACEIs) offer comparable blood pressure control and health outcomes. ARBs are associated with fewer adverse events and less cough.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology
  • Clinical Effectiveness Research

Background:

  • Hypertension is a prevalent chronic condition in the USA.
  • The renin-angiotensin system (RAS) is a key target for antihypertensive therapies.
  • Primary RAS blockade strategies include direct renin inhibitors, ACEIs, and ARBs.

Purpose of the Study:

  • To summarize a direct comparative effectiveness review of trials comparing antihypertensive medications.
  • To evaluate the comparative effectiveness and safety of ACEIs, ARBs, and direct renin inhibitors in patients with hypertension.

Main Methods:

  • Systematic review and meta-analysis of direct comparative trials.
  • Focused on studies involving patients with hypertension.

Main Results:

  • ACEIs and ARBs demonstrated similar effects on blood pressure and overall health outcomes.
  • Angiotensin receptor blockers (ARBs) showed a lower incidence of ACE-induced cough and fewer adverse event-related withdrawals compared to ACEIs.
  • Data comparing direct renin inhibitors with ACEIs or ARBs were limited, leaving their comparative role less defined.

Conclusions:

  • ACEIs and ARBs represent effective and comparable therapeutic options for managing hypertension.
  • ARBs offer a potential advantage in terms of tolerability due to reduced cough and adverse event withdrawals.
  • Further research is needed to clarify the role of direct renin inhibitors in hypertension management.

Related Concept Videos

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,...
1.9K
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...
2.7K
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...
2.1K
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...
3.0K