Myocardial transit time mapping by CMR: A novel potential parameter of microcirculatory dysfunction in hypertrophic

Junlin Yang1, Yong Cheng1, Jinxiu Yang1

  • 1Department of Radiology, The First Affiliated Hospital of Anhui Medical University, No.218 Jixi Road, Hefei, Anhui 230022, China.

PubMed

Insights

Myocardial transit time (MyoTT) measured by cardiovascular magnetic resonance (CMR) is elevated in hypertrophic cardiomyopathy (HCM) patients, especially those with atrial fibrillation (AF). This parameter may indicate coronary microvascular dysfunction (CMD) in HCM.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Biophysics

Background:

  • Hypertrophic cardiomyopathy (HCM) is a genetic heart condition often associated with coronary microvascular dysfunction (CMD).
  • Atrial fibrillation (AF) is a common complication in HCM patients, potentially worsening prognosis.
  • Current methods for assessing CMD in HCM have limitations.

Purpose of the Study:

  • To investigate myocardial transit time (MyoTT) using cardiovascular magnetic resonance (CMR) as a potential biomarker for CMD in HCM.
  • To evaluate the association of MyoTT with HCM and AF status.
  • To compare the diagnostic performance of MyoTT with other CMR-derived parameters.

Main Methods:

  • A cohort of 50 HCM patients and 50 healthy controls underwent CMR scans.
  • Parameters assessed included cardiac function, native T1, extracellular volume (ECV), myocardial strain, and MyoTT.
  • Logistic regression and receiver operating characteristic (ROC) analyses were used to evaluate associations and discriminative performance.

Main Results:

  • HCM patients showed significantly altered cardiac function, increased native T1, ECV, and MyoTT compared to controls.
  • MyoTT, native T1, ECV, and LV-GLS were significantly associated with HCM status.
  • In HCM patients, higher native T1 and MyoTT values were observed in those with AF.
  • MyoTT demonstrated good discriminative performance for HCM (AUC=0.848) and for AF within HCM (AUC=0.740).

Conclusions:

  • MyoTT is elevated in HCM patients and is associated with the presence of AF.
  • MyoTT may serve as a valuable non-invasive imaging marker for CMD in HCM, particularly in the context of AF.
  • Further research is warranted to explore the clinical implications of MyoTT in HCM management.
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...
433
Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
11.7K
Amyloid Fibrils03:03

Amyloid Fibrils

6.4K
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,...
492
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...
488
Phase Transitions02:31

Phase Transitions

Whether solid, liquid, or gas, a substance's state depends on the order and arrangement of its particles (atoms, molecules, or ions). Particles in the solid pack closely together, generally in a pattern. The particles vibrate about their fixed positions but do not move or squeeze past their neighbors. In liquids, although the particles are closely spaced, they are randomly arranged. The position of the particles are not fixed—that is, they are free to move past their neighbors to...
22.8K