Myocardial catecholamine concentrations in dilated cardiomyopathy and heart failure of different origins

V Regitz1, B Leuchs, C Bossaller

  • 1Abteilung für Innere Medizin/Kardiologie, Deutsches Herzzentrum Berlin, Germany.

European Heart Journal
|August 1, 1991
PubMed

Insights

Heart failure significantly reduces myocardial norepinephrine levels, a key neurotransmitter. This reduction is consistent across different heart disease causes and correlates with impaired left ventricular function.

Area of Science:

  • Cardiology
  • Neuroscience
  • Biochemistry

Background:

  • Myocardial catecholamine levels are crucial in heart function and disease.
  • Previous research suggests altered catecholamine levels in heart failure, but direct tissue measurements and their correlation with disease severity are less understood.

Purpose of the Study:

  • To investigate myocardial catecholamine concentrations in patients with heart failure.
  • To determine if these levels correlate with the severity of myocardial damage or the underlying disease aetiology.

Main Methods:

  • Endomyocardial biopsies were obtained from patients with heart failure.
  • Catecholamine concentrations were measured and normalized to non-collagen protein (NCP).
  • Levels were compared between patient groups and with controls, and correlated with left ventricular ejection fraction (LVEF).

Main Results:

  • Myocardial norepinephrine levels were significantly reduced in heart failure patients compared to controls (P < 0.0006).
  • Norepinephrine levels were comparable in dilated cardiomyopathy and coronary/valvular heart disease groups.
  • Lower norepinephrine levels were observed in patients with LVEF < 30% compared to those with LVEF 31-55% (P < 0.05).
  • A strong correlation was found between myocardial norepinephrine and LVEF in dilated cardiomyopathy (P < 0.001, r = 0.70).

Conclusions:

  • Reduced myocardial norepinephrine is a hallmark of heart failure, irrespective of its cause.
  • The depletion of myocardial norepinephrine is associated with the severity of left ventricular dysfunction.

Related Concept Videos

Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
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...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...