Endothelial function and arterial compliance are not impaired in subjects with heart failure of non-ischemic origin

Ashish Shah1, Eugenia Gkaliagkousi, James M Ritter

  • 1Department of Clinical Pharmacology, Cardiovascular Division, School of Medicine, King's College London, London, UK.

Journal of Cardiac Failure
|February 10, 2010
PubMed

Insights

Heart failure without ischemic heart disease does not show endothelial dysfunction or arterial stiffness. Non-ischemic heart failure patients had normal flow-mediated dilation and vascular compliance, unlike those with ischemic heart disease.

Area of Science:

  • Cardiology
  • Vascular Biology
  • Heart Failure Research

Background:

  • Patients with heart failure and ischemic heart disease (IHD) often have endothelial dysfunction and increased arterial stiffness.
  • This study investigated if these vascular abnormalities are present in heart failure of nonischemic origin.

Purpose of the Study:

  • To compare endothelial function and arterial stiffness in patients with heart failure due to ischemic heart disease (IHD) versus nonischemic dilated cardiomyopathy (DCM).
  • To determine if nonischemic heart failure is associated with endothelial dysfunction or increased arterial stiffness.

Main Methods:

  • Compared 11 IHD patients, 12 DCM patients, and 16 healthy controls.
  • Assessed endothelium-dependent (flow-mediated dilation, FMD) and independent (glyceryl trinitrate, GTN) function via brachial artery ultrasound.
  • Measured vascular compliance using carotid-femoral pulse wave velocity (PWV) and augmentation index (AIx).

Main Results:

  • FMD was impaired in IHD patients but not in DCM patients compared to controls.
  • PWV was increased in IHD patients but not in DCM patients compared to controls.
  • GTN-induced dilatation and AIx were similar across all groups.

Conclusions:

  • Heart failure of nonischemic etiology (DCM) is not associated with endothelial dysfunction or abnormal arterial compliance.
  • These findings suggest distinct pathophysiological mechanisms in ischemic versus nonischemic heart failure.
  • Larger studies are needed to confirm these results.
Abstract

Related Concept Videos

Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
Heart Failure I: Introduction01:27

Heart Failure I: Introduction

Heart failure refers to a clinical syndrome caused by structural or functional cardiac disorders that prevent the heart from pumping an adequate amount of blood to meet the body's metabolic needs. This condition often arises from myocardial infarction or ischemia, leading to decreased cardiac output, reduced tissue perfusion, impaired gas exchange, fluid volume imbalance, and decreased functional ability.Heart failure can result from disruptions in the mechanisms that regulate cardiac output...
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...
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...
Imbalances in Cardiac Output01:26

Imbalances in Cardiac Output

The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send blood...