Aortic elastic properties : effects of carvedilol versus nebivolol

M R Sayin1, M Aydin, S M Dogan

  • 1Department of Cardiology, Bülent Ecevit University, Zonguldak, Turkey. sayinmr@mynet.com

Herz
|December 25, 2012
PubMed

Insights

This study found that both carvedilol and nebivolol effectively lowered blood pressure and heart rate in patients with hypertension. While nebivolol showed a slight edge in improving heart function, neither drug significantly altered aortic elastic properties.

Area of Science:

  • Cardiology
  • Pharmacology
  • Hypertension Management

Background:

  • Aortic elastic properties are crucial indicators of cardiovascular morbidity and mortality in hypertension.
  • Newer generation beta-blockers, such as carvedilol and nebivolol, offer potential therapeutic benefits for hypertensive patients.
  • Understanding their impact on vascular elasticity is essential for optimizing treatment strategies.

Purpose of the Study:

  • To compare the effects of carvedilol and nebivolol on aortic elastic properties in patients with stage 1 hypertension.
  • To evaluate changes in aortic strain (AS), aortic distensibility (AD), and aortic stiffness index (ASI) following treatment.
  • To assess the comparative efficacy of these beta-blockers on hemodynamic parameters and cardiac function.

Main Methods:

  • A randomized study involving 47 treatment-naive stage 1 hypertensive patients.
  • Participants received either carvedilol (25 mg/day) or nebivolol (5 mg/day) for 3 months.
  • Aortic elastic parameters were measured using echocardiography.

Main Results:

  • Both carvedilol and nebivolol significantly reduced systolic and diastolic blood pressure and heart rate.
  • Improvements in left ventricular diastolic function were observed in both groups, with nebivolol showing a slight advantage.
  • While aortic elastic properties showed a trend towards improvement with both drugs, these changes were not statistically significant.

Conclusions:

  • Carvedilol and nebivolol are effective in lowering blood pressure and heart rate and improving left ventricular diastolic function in hypertensive patients.
  • Neither drug significantly impacted aortic elastic properties, though nebivolol demonstrated a slightly greater benefit.
  • Further long-term studies with larger cohorts are warranted to fully elucidate the vascular effects of these agents.
Abstract

Related Concept Videos

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, vasodilation, and...
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 clinically...
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 vasodilation. This widens airways and...
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, β1-blockers...
Antihypertensive Drugs: Vasodilators01:23

Antihypertensive Drugs: Vasodilators

Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
Antianginal Drugs: Nitrates and β-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. Administered...