Abnormal left ventricular contraction sequence in hypertrophic cardiomyopathy patients: first description of

Josselin Duchateau1, Claire Cornolle1, Jérome Peyrou1

  • 1Unité des cardiopathies valvulaires et laboratoire d'échocardiographie, Hôpital Cardiologique du Haut Lévèque, Pessac, France.

Insights

Hypertrophic cardiomyopathy (HCM) alters the normal sequence of left ventricular contraction, causing a loss of the apex-to-base delay (ABD) essential for efficient heart function. This change in cardiac mechanics is independent of other clinical factors.

Area of Science:

  • Cardiology
  • Biomedical Engineering
  • Cardiac Physiology

Background:

  • Normal left ventricular contraction exhibits an apex-to-base delay (ABD), a form of physiologic asynchrony crucial for efficient cardiac mechanics.
  • Hypertrophic cardiomyopathy (HCM) is a condition affecting the heart muscle, potentially altering its contraction patterns.

Purpose of the Study:

  • To compare the left ventricular contraction sequence in patients with HCM and healthy individuals.
  • To investigate the presence and significance of apex-to-base delay (ABD) in HCM patients.

Main Methods:

  • Prospective analysis of echocardiographic data from 40 HCM patients and 20 healthy controls.
  • Measurement of endocardial longitudinal and circumferential strains and ABD using custom software.
  • Statistical comparison of strain parameters and ABD between HCM patients and controls.

Main Results:

  • HCM patients demonstrated increased circumferential strain and decreased longitudinal strain compared to controls.
  • Physiologic ABD was observed in healthy controls (35.7 ± 18.1 ms).
  • HCM patients showed a significantly reduced ABD (5.5 ± 22.7 ms) compared to controls, indicating a loss of normal contraction sequencing.

Conclusions:

  • Left ventricular contraction sequence is modified in HCM patients, characterized by the loss of physiologic apex-to-base delay.
  • The observed alteration in contraction sequence in HCM is independent of commonly measured clinical and echocardiographic parameters.

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...
801
Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
5.4K
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
1.5K
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,...
805
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...
869
The Cardiac Cycle01:13

The Cardiac Cycle

The heart beats rhythmically in a sequence called the cardiac cycle—a rapid coordination of contraction (systole) and relaxation (diastole).
The Process
Electrical signals—sent from the sinoatrial (SA) node in the right atrial wall to the atrioventricular (AV) node between the right atrium and right ventricle—cause both atria to simultaneously contract. When the signal reaches the AV node, it pauses for approximately a tenth of a second, allowing the atria to contract and...
102.3K