[Heart rate variability in patients with hypertension and type 2 diabetes treated with long acting calcium

Kardiologiia
|August 2, 2003
PubMed

Insights

Calcium antagonists may increase sympathetic activity, potentially raising cardiovascular risks in patients with hypertension and type 2 diabetes. This heart rate variability study suggests careful consideration of treatment options.

Area of Science:

  • Cardiology
  • Pharmacology
  • Hypertension Management

Background:

  • Enhanced sympathetic activity is linked to cardiovascular complications in hypertension and type 2 diabetes.
  • Understanding the impact of antihypertensive medications on sympathetic activity is crucial.

Purpose of the Study:

  • To investigate the effect of calcium antagonists on sympathetic activity.
  • To assess changes in heart rate variability (HRV) during calcium antagonist treatment.

Main Methods:

  • Assessed heart rate variability (HRV) in 89 hypertensive patients.
  • Patients received 12-16 weeks of treatment with various long-acting calcium antagonists.
  • Monitored 24-hour blood pressure and analyzed HRV parameters.

Main Results:

  • Calcium antagonist treatment was associated with enhanced sympathetic activity, indicated by HRV changes.
  • Verapamil showed a favorable effect on morning blood pressure rise compared to other calcium antagonists.
  • Nifedipine and dihydropyridines demonstrated greater sympathetic enhancement than verapamil.

Conclusions:

  • Calcium antagonists negatively affect HRV parameters, suggesting increased sympathetic activity.
  • This finding necessitates careful selection of antihypertensive therapy for patients with hypertension and type 2 diabetes.
  • Consideration of HRV changes is important when prescribing calcium antagonists.
Abstract

Related Concept Videos

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which indirectly block calcium...
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
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,...
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...
Hypertension IV: Drug Therapy and Lifestyle Modifications01:28

Hypertension IV: Drug Therapy and Lifestyle Modifications

Multiple classes of antihypertensive medications are employed in treating hypertension. The most commonly recommended first-line treatments include:Thiazide Diuretics, such as chlorthalidone, increase sodium and water excretion from the body, reducing blood volume and blood pressure.Angiotensin-converting enzyme inhibitors, like lisinopril, block the conversion of angiotensin I to II, a potent vasoconstrictor lowering blood pressure.Angiotensin II Receptor Blockers (ARBs) prevent angiotensin II...
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...