Three-dimensional Mapping of Fibrosis Distribution in Desmoplakin Cardiomyopathy from Cardiac MRI

Javiera Jilberto1,2, Brennen McManus1, Ahmad Moghrabi1

  • 1Department of Biomedical Engineering, University of Michigan, 2200 Bonisteel Blvd, Ann Arbor, MI 48109.

Insights

High-resolution fibrosis mapping in desmoplakin cardiomyopathy using universal ventricular coordinates reveals distinct spatial patterns. Increased fibrosis correlates with impaired left ventricular function and dilatation.

Area of Science:

  • Cardiovascular Imaging
  • Cardiac Pathology
  • Computational Anatomy

Background:

  • Desmoplakin cardiomyopathy is a genetic heart condition characterized by progressive cardiac dysfunction.
  • Accurate spatial characterization of myocardial fibrosis is crucial for understanding disease progression and prognosis.
  • Current imaging techniques may lack the resolution to fully delineate fibrotic patterns in relation to ventricular geometry.

Purpose of the Study:

  • To develop and apply high-resolution fibrosis mapping using universal ventricular coordinates.
  • To spatially characterize fibrotic patterns across varying severities of desmoplakin cardiomyopathy.
  • To correlate fibrosis burden with left ventricular structure and function.

Main Methods:

  • Retrospective analysis of cardiac MRI data from 29 patients with desmoplakin cardiomyopathy.
  • Three-dimensional ventricular model reconstruction from cine MRI.
  • Mapping of late gadolinium enhancement (LGE) identified fibrosis to universal ventricular coordinates for spatial analysis.
  • Classification of disease severity (mild, moderate, severe) based on fibrosis extent.
  • Statistical evaluation of associations between fibrosis burden and left ventricular metrics.

Main Results:

  • Fibrosis patterns varied with disease severity, starting subepicardially in mild cases and progressing to circumferential involvement in severe cases.
  • Significant negative correlation between fibrosis burden and left ventricular ejection fraction (r = -0.80, P < .001).
  • Significant positive correlation between fibrosis burden and left ventricular end-diastolic volume index (r = 0.54, P = .002).
  • Distinct differences in cardiac metrics were observed between moderate and severe disease groups.

Conclusions:

  • Universal ventricular coordinates facilitate high-resolution fibrosis mapping in desmoplakin cardiomyopathy.
  • Characteristic spatial fibrosis patterns emerge with increasing disease severity.
  • Higher fibrosis burden is associated with left ventricular dilatation and reduced systolic function, even in non-dilated ventricles.

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