Left atrial dysfunction in different morphologic phenotypes of hypertrophic cardiomyopathy: a cardiac magnetic

Yiyuan Gao1,2, Wenqi Liu2, Zhan Feng3

  • 1Department of Radiology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Insights

Hypertrophic cardiomyopathy (HCM) patients show impaired left atrial (LA) function across subtypes. Concentric HCM exhibits more severe LA dysfunction than septal HCM, highlighting subtype-specific mechanics.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Biomedical Engineering

Background:

  • Hypertrophic cardiomyopathy (HCM) presents diverse phenotypes, but left atrial (LA) function differences among subtypes are not well understood.
  • Cardiac magnetic resonance feature tracking (CMR-FT) can quantify LA deformation, but its use for subtype-specific mechanics is limited.

Purpose of the Study:

  • To investigate LA functional impairment in different HCM phenotypic subtypes using CMR-FT.
  • To characterize subtype-specific alterations in atrial mechanics.

Main Methods:

  • Retrospective analysis of 225 HCM patients (septal, apical, concentric) and 68 healthy controls (HC).
  • LA functional parameters (reservoir strain εs, conduit strain εe, booster strain εa) measured using CMR-FT.
  • Statistical analysis including ANOVA and regression to compare LA function and correlate with left ventricular parameters.

Main Results:

  • All HCM subgroups displayed significantly impaired LA strain compared to HC (P<0.05).
  • Concentric HCM showed more severe LA reservoir (εs) and booster (εa) strain impairment than septal HCM (P<0.05).
  • CMR-FT demonstrated excellent reproducibility for LA strain measurements (ICCs >0.75).

Conclusions:

  • Left atrial dysfunction varies significantly across HCM phenotypes.
  • Concentric HCM exhibits greater impairment in LA reservoir and booster function compared to septal HCM.
  • CMR-FT is a valuable tool for phenotypic characterization of HCM by assessing subtype-specific atrial mechanics.
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...
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
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...
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...