Apical hypertrophic cardiomyopathy: prevalence and correlates of apical outpouching

Josepha Binder1, Christine H Attenhofer Jost, Kyle W Klarich

  • 1Department of Cardiology, Medical University, Graz, Austria.

Insights

Apical hypertrophic cardiomyopathy (ApHCM) patients with apical outpouching showed no increased risk of major cardiac events. Cardiac complications were common but not linked to apical outpouching in this ApHCM analysis.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Genetics

Background:

  • Apical hypertrophic cardiomyopathy (ApHCM) is characterized by apical wall thickening.
  • Apical outpouching, including wall motion abnormalities and aneurysms, has been described in ApHCM.
  • The clinical significance of apical outpouching in ApHCM remains unclear.

Purpose of the Study:

  • To investigate the prevalence and clinical implications of apical outpouching in patients with ApHCM.
  • To determine if apical outpouching is associated with adverse cardiac events in ApHCM patients.

Main Methods:

  • Retrospective analysis of 193 patients diagnosed with ApHCM between 1976 and 2006.
  • Evaluation of apical outpouching using echocardiography, including contrast-enhanced studies.
  • Assessment of clinical outcomes, including mortality, sudden cardiac death, and arrhythmias during follow-up.

Main Results:

  • Apical outpouching was identified in 15% of ApHCM patients, with higher prevalence (28%) in contrast echocardiography.
  • Patients with apical outpouching had more diastolic gradients, prolonged QT intervals, increased apical wall thickness, and family history of sudden cardiac death.
  • No significant difference in overall mortality, sudden cardiac death, or other major adverse cardiac events was observed between ApHCM patients with and without apical outpouching.

Conclusions:

  • Cardiac complications are frequent in ApHCM patients.
  • Apical outpouching in ApHCM does not appear to be associated with an increased risk of major adverse cardiac events in this study.
  • Further research is needed to fully understand the impact of true apical aneurysms in ApHCM.
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...
Aneurysm I: Introduction01:30

Aneurysm I: Introduction

An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
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...
Aortic Regurgitation II: Clinical Features and Diagnostic Tests01:22

Aortic Regurgitation II: Clinical Features and Diagnostic Tests

Aortic valve regurgitation (AR) occurs when the aortic valve fails to close properly, allowing blood to flow backward from the aorta into the left ventricle. This backflow can result in two distinct clinical presentations: acute and chronic AR, each characterized by its own set of symptoms and physical findings.Acute Aortic RegurgitationAcute AR presents with a sudden onset of severe symptoms. Patients typically experience profound dyspnea (shortness of breath), chest pain, and signs of left...
Mitral Valve Prolapse I: Introduction01:27

Mitral Valve Prolapse I: Introduction

IntroductionThe mitral valve, one of the heart's four valves, regulates blood flow. These valves have flaps that open and close to direct blood properly through the heart and body. During each heartbeat, the flaps open for blood to pass through and seal shut to prevent backflow. Specifically, the mitral valve opens to allow blood flow from the heart's upper left chamber to the lower left chamber. It then closes securely as the lower left chamber contracts to pump blood to the body, preventing...
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,...