Prognostic Impact of Hypertrabeculation and Noncompaction Phenotype in Dilated Cardiomyopathy: A CMR Study

Mihaela-Silvia Amzulescu1, Michel F Rousseau1, Sylvie A Ahn1

  • 1Division of Cardiology, Department of Cardiovascular Diseases, Cliniques Universitaires St. Luc and Pôle de Recherche Cardiovasculaire, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Brussels, Belgium.

Insights

The degree of left ventricular (LV) myocardial noncompaction, assessed by cardiac magnetic resonance (CMR), does not impact cardiovascular outcomes in patients with nonischemic dilated cardiomyopathy (DCM). This suggests noncompaction is not a marker of a more severe DCM form.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Heart Failure Research

Background:

  • Myocardial trabeculations and noncompaction are increasingly recognized in dilated cardiomyopathy (DCM) patients.
  • The prognostic significance of these findings in DCM remains unclear.

Purpose of the Study:

  • To determine the impact of hypertrabeculation and left ventricular (LV) myocardial noncompaction, identified via cardiac magnetic resonance (CMR), on outcomes in nonischemic DCM.
  • To assess if the degree of noncompaction indicates a more severe form of DCM.

Main Methods:

  • Prospective evaluation of 162 patients with nonischemic DCM using CMR.
  • Quantification of noncompaction using noncompacted/compacted (NC/C) length and mass ratios.
  • Comparison with 48 healthy controls and analysis of major adverse cardiovascular events (MACE) over a median follow-up of 3.4 years.

Main Results:

  • 36% of DCM patients exhibited increased NC/C length, and 44% had increased NC/C mass.
  • Neither NC/C length nor mass correlated with clinical, echocardiographic, or CMR parameters.
  • Multivariate analysis identified LV ejection fraction (EF) and late gadolinium enhancement as independent predictors of MACE; NC/C ratios did not predict outcomes.

Conclusions:

  • The extent of trabeculation in adult patients with nonischemic DCM does not appear to influence cardiovascular outcomes.
  • Findings suggest that a noncompaction phenotype does not signify a more severe form of DCM.
Abstract

Related Concept Videos

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...
741
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,...
776
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...
664
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...
830
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...
3.4K
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...
1.4K