Bempedoic Acid: A New Tool for LDL-Cholesterol Control in Patients with Coronary Artery Disease

Claudio Bilato1, Giorgio Sesti2, Maurizio Averna3

  • 1Division of Cardiology, West Vicenza General Hospitals, 36071 Arzignano-Vicenza, Italy.

Insights

Bempedoic acid effectively lowers LDL-cholesterol in patients unable to reach targets with other therapies. This new oral agent offers a well-tolerated option for managing atherosclerotic cardiovascular disease risk.

Area of Science:

  • Cardiology
  • Pharmacology
  • Biochemistry

Background:

  • Many patients with high atherosclerotic cardiovascular disease (ASCVD) risk do not achieve target LDL-cholesterol levels.
  • Challenges include drug intolerance, poor adherence, and limitations of current stepwise lipid-lowering strategies.

Purpose of the Study:

  • To evaluate the efficacy and safety of bempedoic acid as an add-on therapy for LDL-cholesterol reduction in high-risk patients.

Main Methods:

  • Bempedoic acid inhibits adenosine triphosphate-citrate lyase, an enzyme in cholesterol synthesis.
  • Clinical trials assessed bempedoic acid alone or in combination with statins and/or ezetimibe.
  • Activation is liver-specific, minimizing skeletal muscle side effects.

Main Results:

  • Bempedoic acid significantly reduced LDL-cholesterol and high-sensitivity C-reactive protein in clinical trials.
  • The drug was well-tolerated, with no significant increase in muscle-related symptoms.
  • Effective in patients not reaching LDL-cholesterol goals despite maximally tolerated lipid-lowering therapy.

Conclusions:

  • Bempedoic acid is a valuable oral agent for further reducing LDL-cholesterol in high-risk ASCVD patients.
  • It offers an effective and well-tolerated treatment option for patients with suboptimal lipid management.
  • Addresses unmet needs in managing hypercholesterolemia and reducing cardiovascular risk.

Related Concept Videos

Lipid-Lowering Drugs: Statins and Miscellaneous Agents01:20

Lipid-Lowering Drugs: Statins and Miscellaneous Agents

Hyperlipidemia, a medical condition often referred to as high cholesterol, is characterized by abnormally elevated levels of lipids in the bloodstream. When present in excess, these lipids, specifically cholesterol and triglycerides, can lead to serious health complications, often involving cardiovascular diseases. Illnesses like atherosclerosis, heart attacks, and pancreatitis have all been linked to untreated hyperlipidemia. This means controlling and regulating cholesterol and triglyceride...
613
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
481
Adrenergic Antagonists: ɑ and β-Receptor Blockers01:31

Adrenergic Antagonists: ɑ and β-Receptor Blockers

Third-generation β-blockers, such as labetalol and carvedilol, represent a significant advancement in managing cardiovascular conditions. Unlike conventional β-blockers, which can induce peripheral vasoconstriction, third-generation drugs block α1 adrenoceptors. This promotes vasodilation through several mechanisms, such as increased nitric oxide production, inhibition of calcium ion entry, opening of potassium ion channels, and antioxidant action. Labetalol, for instance, is...
429
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...
413
Antihypertensive Drugs: Action of Calcium Channel Blockers01:18

Antihypertensive Drugs: Action of Calcium Channel Blockers

Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
483
Heart Failure Drugs: β-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,...
332