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Updated: Aug 6, 2026

3D Whole-heart Myocardial Tissue Analysis
Published on: April 12, 2017
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.
Abstract:
Purpose To generate high-resolution fibrosis maps using universal ventricular coordinates for spatial characterization of fibrotic patterns across disease severity in desmoplakin cardiomyopathy. Materials and Methods This retrospective study included patients with desmoplakin cardiomyopathy who underwent cardiac MRI between March 2012 and October 2024. Three-dimensional ventricular models were reconstructed from cine MRI acquisitions. Fibrosis identified at late gadolinium enhancement MRI was mapped to ventricular geometry using universal ventricular coordinates, enabling analysis within a common reference framework. Patients were classified as having mild, moderate, or severe disease based on fibrosis extent. Associations between fibrosis burden and left ventricular structural and functional metrics were evaluated using Tukey and Wald tests. Results Twenty-nine patients (mean age, 37.39 years [range, 10-77 years]; 20 female patients) were included. In mild disease, fibrosis was primarily located in the subepicardial midinferior region. With increasing fibrosis burden, moderate and severe disease demonstrated subepicardial circumferential involvement with a ringlike pattern in severe cases. Fibrosis burden correlated negatively with left ventricular ejection fraction (r = -0.80, P < .001) and positively with left ventricular end-diastolic volume index (r = 0.54, P = .002). Group comparisons showed significant differences between moderate and severe disease groups across all metrics (P < .05) but not between mild and moderate groups. Conclusion Use of universal ventricular coordinates enabled high-resolution mapping of fibrosis and demonstrated characteristic spatial patterns across disease severity in desmoplakin cardiomyopathy. Fibrosis was observed in nondilated ventricles, whereas higher fibrosis burden was associated with left ventricular dilatation and impaired systolic function. Keywords: Cardiomyopathies, Left Ventricle, Computer Applications-3D, MR Imaging Supplemental material is available for this article. © RSNA, 2026.
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