[Hypertrophic cardiomyopathy and viral, idiopathic myopericarditis]

Klinicheskaia Meditsina
|October 29, 2000
PubMed

Insights

Viral myopericarditis can lead to hypertrophic cardiomyopathy, often presenting asymptomatically. This study highlights the long-term cardiac changes following myopericarditis.

Area of Science:

  • Cardiology
  • Infectious Diseases
  • Genetics

Background:

  • Myopericarditis, inflammation of the heart muscle and outer lining, can be triggered by viral infections or have idiopathic causes.
  • Long-term sequelae of myopericarditis are not fully understood, necessitating further investigation into potential chronic cardiac conditions.

Observation:

  • A cohort of 64 patients with a history of acute myopericarditis was followed for 3 to 24 years.
  • Echocardiography revealed asymmetric septal hypertrophy in 10 patients, indicative of hypertrophic cardiomyopathy.

Findings:

  • Hypertrophic cardiomyopathy developed in 10 of 64 patients post-myopericarditis.
  • The condition often remained asymptomatic or presented with minimal symptoms, underscoring the challenge in early detection.
  • Laboratory and functional investigations during acute myopericarditis are presented.

Implications:

  • Viral infections may play a role in the pathogenesis of hypertrophic cardiomyopathy.
  • The findings suggest a need for long-term cardiac monitoring in patients with a history of myopericarditis.
  • Understanding the relationship between viral infections and cardiomyopathy can inform future diagnostic and therapeutic strategies.

Related Concept Videos

Myocarditis I: Introduction01:21

Myocarditis I: Introduction

Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
Myocarditis II: Clinical Features and Diagnostic Tests01:27

Myocarditis II: Clinical Features and Diagnostic Tests

Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...
Myocarditis III: Medical Management01:14

Myocarditis III: Medical Management

Myocarditis: Comprehensive Medical ManagementMyocarditis, the heart muscle inflammation, requires a comprehensive medical management strategy that addresses the underlying cause, provides supportive care, manages symptoms, and reduces cardiac workload.Infections and Autoimmune CausesAdminister appropriate antimicrobial therapy when an infectious agent causes myocarditis. For instance, penicillin treats infections caused by Group A Streptococcus. In cases where autoimmune processes are...
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...