Effect of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers After Coronary Artery Bypass

Arden R Barry1,2, Hamed Helisaz3,4, Abdollah Safari3,5

  • 1Faculty of Pharmaceutical Sciences The University of British Columbia Vancouver British Columbia Canada.

Insights

Angiotensin-converting enzyme inhibitors/angiotensin receptor blockers (ACEI/ARBs) reduced major adverse cardiovascular events (MACE) in patients after coronary artery bypass graft surgery. This benefit was observed regardless of heart failure status, indicating broad cardiovascular protection.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology
  • Health Services Research

Background:

  • The impact of ACEI/ARBs on MACE post-coronary artery bypass graft (CABG) surgery remains unclear.
  • This study investigates ACEI/ARB use and MACE in a large Canadian population undergoing CABG.

Purpose of the Study:

  • To evaluate the association between ACEI/ARB exposure and MACE in patients following CABG surgery.
  • To determine if heart failure (HF) status modifies the effect of ACEI/ARBs on MACE.

Main Methods:

  • Retrospective, population-based cohort study using linked administrative health data.
  • Included 15,439 adult patients undergoing CABG between 2002-2020.
  • Primary outcome: time to MACE (all-cause death, MI, ischemic stroke) analyzed with Cox models and inverse probability treatment weighting.

Main Results:

  • 40% of patients received ACEI/ARBs; 16% had pre-existing heart failure.
  • ACEI/ARB exposure was associated with significantly lower MACE risk at 1 and 5 years post-CABG.
  • The protective effect was evident in both patients with and without heart failure (interaction P <0.0001).

Conclusions:

  • ACEI/ARBs are associated with reduced MACE in patients post-CABG.
  • This benefit is consistent across patients with and without heart failure.
  • Findings support the use of ACEI/ARBs in CABG patients for cardiovascular risk reduction.
Abstract

Related Concept Videos

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...
421
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...
711
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...
617
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,...
585
Antianginal Drugs: Nitrates and &#946;-Blockers01:16

Antianginal Drugs: Nitrates and β-Blockers

In cardiovascular health, antianginal drugs combat angina pectoris — a condition marked by chest pain owing to diminished blood flow to the heart.
Organic nitrates,  such as nitroglycerin, play a pivotal role. Once metabolized, they liberate nitric oxide, a molecular marvel. Nitric oxide triggers guanylyl cyclase and augments cGMP production. This biochemical cascade orchestrates the relaxation of vascular smooth muscles, ushering in vasodilation and enhancing coronary blood flow....
573
Heart Failure Drugs: &#946;-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
336