Abstract

BackgroundQuantification of non-ischemic myocardial scar remains a challenge due to the patchy diffuse nature of fibrosis. Extracellular volume (ECV) to guide late gadolinium enhancement (LGE) analysis may achieve a robust scar assessment.MethodsThree cohorts of 80 non-ischemic-training, 20 non-ischemic-validation, and 10 ischemic-validation were prospectively enrolled and underwent 3.0 Tesla cardiac MRI. An ECV cutoff to differentiate LGE scar from non-scar was identified in the training cohort from the receiver-operating characteristic curve analysis, by comparing the ECV value against the visually-determined presence/absence of the LGE scar at the highest signal intensity (SI) area of the mid-left ventricle (LV) LGE. Based on the ECV cutoff, an LGE semi-automatic threshold of n-times of standard-deviation (n-SD) above the remote-myocardium SI was optimized in the individual cases ensuring correspondence between LGE and ECV images. The inter-method agreement of scar amount in comparison with manual (for non-ischemic) or full-width half-maximum (FWHM, for ischemic) was assessed. Intra- and inter-observer reproducibility were investigated in a randomly chosen subset of 40 non-ischemic and 10 ischemic cases.ResultsThe non-ischemic groups were all female with the HIV positive rate of 73.8% (training) and 80% (validation). The ischemic group was all male with reduced LV function. An ECV cutoff of 31.5% achieved optimum performance (sensitivity: 90%, specificity: 86.7% in training; sensitivity: 100%, specificity: 81.8% in validation dataset). The identified n-SD threshold varied widely (range 3 SD–18 SD), and was independent of scar amount (β = −0.01, p = 0.92). In the non-ischemic cohorts, results suggested that the manual LGE assessment overestimated scar (%) in comparison to ECV-guided analysis [training: 4.5 (3.2–6.4) vs. 0.92 (0.1–2.1); validation: 2.5 (1.2–3.7) vs. 0.2 (0–1.6); P < 0.01 for both]. Intra- and inter-observer analyses of global scar (%) showed higher reproducibility in ECV-guided than manual analysis with CCC = 0.94 and 0.78 versus CCC = 0.86 and 0.73, respectively (P < 0.01 for all). In ischemic validation, the ECV-guided LGE analysis showed a comparable scar amount and reproducibility with the FWHM.ConclusionsECV-guided LGE analysis is a robust scar quantification method for a non-ischemic cohort.Trial registration ClinicalTrials.gov; NCT00000797, retrospectively-registered 2 November 1999; NCT02501811, registered 15 July 2015.

Highlights

  • Quantification of non-ischemic myocardial scar remains a challenge due to the patchy diffuse nature of fibrosis

  • A–D Case 1, which presented with scar on Extracellular volume (ECV)-guided late gadolinium enhancement (LGE) analysis

  • E–H Case 2, which presented without scar on ECV-guided LGE analysis

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Summary

Introduction

Quantification of non-ischemic myocardial scar remains a challenge due to the patchy diffuse nature of fibrosis. A number of LGE scar quantification methods with semi-automated thresholds have been proposed and utilized [5, 9, 17,18,19,20,21,22,23] These methods use a fixed calculation formula to define a signal intensity (SI) threshold value above which the tissue is identified as a myocardial scar. Their performance is well recognized in ischemic cases while in non-ischemic cases, it is not infrequent that substantial manual correction is needed after semi-automated thresholding. Manual analysis is challenging as the nonischemic patchy fibrosis presents a rather low contrast on LGE when compared to the ischemic dense fibrotic scar [24]

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