Noncircumferential myofiber function: impact on early diastolic filling in children

E C Michelfelder1, P Khoury, S A Witt

  • 1Noninvasive Cardiac Imaging and Hemodynamic Research Laboratory, Division of Cardiology, Children's Hospital Medical Center, 3333 Burnet Ave., OSB-4, Cincinnati, OH 45229, USA. miche0@chmcc.org

Insights

Oblique myofiber shortening, measured by left ventricular systolic twist (LVST), significantly impacts early diastolic filling in children. This contrasts with circumferential and longitudinal shortening, which showed no relation to diastolic function.

Area of Science:

  • Pediatric Cardiology
  • Cardiac Physiology
  • Echocardiography

Background:

  • Myofiber contraction patterns influence systolic and diastolic function.
  • Understanding noncircumferential fiber mechanics is crucial for assessing global left ventricular function.

Purpose of the Study:

  • To investigate the relationship between circumferential, longitudinal, and oblique left ventricular (LV) fiber shortening and early diastolic filling in children.
  • To determine the impact of LV systolic twist (LVST) on pediatric diastolic function.

Main Methods:

  • Prospective echocardiographic evaluation in 25 healthy children (mean age 8.1 years).
  • Assessment of circumferential (shortening fraction, fractional area change), longitudinal (axial shortening), and oblique (LVST) fiber shortening.
  • Measurement of early diastolic filling parameters, including E-wave acceleration time.

Main Results:

  • No significant correlation was found between early diastolic filling indexes and circumferential or longitudinal shortening.
  • A significant inverse relationship was observed between heart rate-corrected E-wave acceleration time and LVST (r = 0.63, P <.001).

Conclusions:

  • Oblique fiber shortening, specifically LVST, plays a role in early diastolic filling in pediatric populations.
  • Further research into noncircumferential myofiber function can enhance the understanding of overall left ventricular function.

Related Concept Videos

Mitral Stenosis I: Introduction01:22

Mitral Stenosis I: Introduction

Mitral Valve Stenosis (MVS) is a heart condition where the mitral valve narrows, impeding blood circulation from the left atrium to the left ventricle. The etiology and pathophysiology of this condition are multifaceted, leading to a cascade of cardiovascular complications.Causes of Mitral Valve StenosisRheumatic Heart Disease: It is the main cause of mitral valve stenosis, particularly in developing nations. This condition arises from rheumatic fever, an inflammatory illness resulting from...
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...
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...
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...