Absence of enteroviral RNA in hearts explanted from patients with dilated cardiomyopathy

M G Crespo-Leiro1, M Hermida-Prieto, F Peña

  • 1Heart Transplant Programme, Hospital Juan Canalejo and Instituto de Ciencias de la Salud, Universidad de La Coruña, Spain. MarisaCrespo@canalejo.cesga.es

Insights

This study found no evidence of enterovirus in heart tissue from dilated cardiomyopathy (DCM) patients. This suggests enteroviruses may not persist in myocardial tissue during DCM development.

Area of Science:

  • Cardiology
  • Virology
  • Pathogenesis

Background:

  • The link between enterovirus infection and dilated cardiomyopathy (DCM) pathogenesis is not well understood.
  • Investigating enterovirus presence in DCM is crucial for understanding disease mechanisms.

Purpose of the Study:

  • To determine the prevalence of enterovirus in explanted hearts from DCM patients.
  • To compare enterovirus prevalence in DCM hearts versus hearts with other etiologies and healthy donor hearts.

Main Methods:

  • Analyzed 138 cardiac samples (70 healthy donors, 68 transplant recipients including 22 with DCM).
  • Utilized a highly sensitive enterovirus-specific nested reverse transcription-polymerase chain reaction (RT-PCR) for detection.

Main Results:

  • One positive enterovirus test result was observed but attributed to contamination.
  • Sequencing confirmed the single positive result was identical to the positive control, indicating no true viral presence.

Conclusions:

  • No evidence of enteroviral RNA was found in the explanted heart samples using nested RT-PCR.
  • This suggests that if enteroviruses contribute to DCM, they do not persist in myocardial tissue.
Abstract

Related Concept Videos

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 IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
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 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...
Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
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...