Redefining beta-blocker use in hypertension: selecting the right beta-blocker and the right patient

Samuel J Mann1

  • 1NY Presbyterian Hospital-Weill Cornell medicine, New York, USA.

Insights

Beta-blockers are often overused for hypertension. This perspective argues for targeted use in specific patients, particularly those with neurogenic hypertension, and suggests combined alpha/beta-blockers may offer advantages.

Area of Science:

  • Cardiology
  • Pharmacology
  • Hypertension Management

Background:

  • Randomized controlled trials indicate traditional beta-blockers are inferior for initial hypertension treatment compared to other drug classes.
  • Beta-blocker use is linked to adverse effects, leading some guidelines to deem them less suitable for first-line therapy.
  • Despite evidence, beta-blockers remain widely prescribed and potentially overused in hypertension management.

Purpose of the Study:

  • To advocate for a more targeted approach to beta-blocker use in hypertension.
  • To identify specific patient profiles and hypertension mechanisms where beta-blockers are most effective.
  • To highlight the potential benefits of combined alpha/beta-blockers and specific pharmacokinetic properties.

Main Methods:

  • Review of existing randomized controlled trials and clinical guidelines on hypertension treatment.
  • Analysis of hypertension pathophysiology to delineate appropriate beta-blocker patient selection.
  • Evaluation of different beta-blocker subclasses, including combined alpha/beta-blockers and pharmacokinetic considerations.

Main Results:

  • Beta-blockers are generally ineffective for sodium/volume-mediated or renin-angiotensin system-mediated hypertension.
  • They are best suited for sympathetically driven (neurogenic) hypertension, as first-line or add-on therapy.
  • Combined alpha/beta-blockade and non-lipophilic beta-blockers with favorable pharmacokinetics show promise.

Conclusions:

  • Beta-blockers have a valuable role in hypertension but require precise patient and drug selection.
  • Targeting neurogenic hypertension and considering pharmacokinetic profiles can optimize beta-blocker effectiveness.
  • Further research into combined alpha/beta-blockers and specific beta-blocker formulations is warranted.

Related Concept Videos

Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers01:27

Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers

β-receptor blockers significantly impact the cardiovascular system by counteracting catecholamine-induced sympathetic responses. These medications decrease heart rate, contractility, and cardiac output, potentially leading to cardiac depression, life-threatening bradycardia, and death. Therapeutically, β-blockers function as mild antihypertensives and are utilized in treating angina pectoris and cardiac arrhythmias. However, nonselective β-blockers inhibit β2-receptors in...
1.8K
Antihypertensive Drugs: Types of β-Blockers01:28

Antihypertensive Drugs: Types of β-Blockers

β receptors are classified into three subclasses: β1, β2, and β3. β1 receptors are primarily located in the heart and kidneys. When they get activated, they increase heart rate, contractility, and renin release. This process enhances blood pressure and aids in stress management. In contrast, β2 receptors are situated mainly in the lungs, blood vessels, and skeletal muscles. Upon activation, they trigger smooth muscle relaxation, causing bronchodilation and...
1.8K
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,...
1.0K
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...
1.3K
Antihypertensive Drugs: Action of β1 Blockers01:17

Antihypertensive Drugs: Action of β1 Blockers

β1-receptors are primarily located in the heart and kidneys. In cardiac myocytes, these receptors interact with neurotransmitters released by the sympathetic nervous system during heightened activity or danger. As a result, β1-receptors get activated, initiating a series of biochemical processes. Excessive activation of beta receptors due to chronic stress can abnormally increase heart rate and contractility, resulting in high blood pressure or hypertension. To counteract this,...
2.2K
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...
1.6K