Apical hypertrophic cardiomyopathy: clinical and metabolic studies

European Heart Journal
|November 1, 1983
PubMed

Insights

This study describes concentric apical hypertrophy, a type of hypertrophic cardiomyopathy. Patients showed characteristic ECG and echocardiogram findings, with some developing diffuse disease over time.

Area of Science:

  • Cardiology
  • Cardiovascular Diseases
  • Internal Medicine

Background:

  • Hypertrophic cardiomyopathy encompasses various forms, including non-obstructive types.
  • A specific subset presents with concentric apical hypertrophy, characterized by distinct electrocardiogram (ECG) findings.

Purpose of the Study:

  • To characterize patients with concentric apical hypertrophy.
  • To investigate the clinical presentation, diagnostic findings, and potential progression of this cardiomyopathy.

Main Methods:

  • Study included seven patients with giant negative T waves and concentric apical hypertrophy.
  • Diagnostic tools included heart catheterization, M-mode and 2D echocardiography, and coronary angiography.
  • Myocardial metabolism was assessed using atrial pacing and lactate sampling in some patients.

Main Results:

  • No outflow tract obstruction was found; coronary angiography was normal.
  • Ventriculography revealed a spade-like apical configuration with significantly increased apical wall thickness.
  • Myocardial metabolism abnormalities were detected in five patients; follow-up showed progression in some.

Conclusions:

  • Concentric apical hypertrophy is a distinct entity within hypertrophic cardiomyopathies.
  • This condition may progress to diffuse hypertrophic cardiomyopathy, indicated by increased wall thickness over time.
  • Further research is needed to understand the long-term prognosis and management.

Related Concept Videos

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...
828
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,...
798
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...
810
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...
957
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...
761
Cellular Adaptation II: Hypertrophy01:26

Cellular Adaptation II: Hypertrophy

Hypertrophy is the increase in the size of individual cells, resulting in the enlargement of a tissue or organ. Unlike hyperplasia, which involves an increase in cell number, hypertrophy is characterized by an increase in cell volume. This process often occurs in response to higher functional demand or hormonal stimulation, leading to the production of more structural proteins and organelles, thereby enhancing the cells' work capacity.There are two primary types of hypertrophy:...
78