Journal
FRONTIERS IN CARDIOVASCULAR MEDICINE
Volume 9, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fcvm.2022.917180
Keywords
cardiac magnetic resonance (CMR); T1 mapping; LGE imaging; myocardial tissue characterization; magnetic resonance imaging; MRI sequence development
Categories
Funding
- 4TU federation, a NWO Start-up
- ZonMW Off-Road [t STU.019.024]
- NIH [04510011910073]
- NSF CAREER CCF [R01HL153146, R21EB028369, P41EB027061]
- AHA Predoctoral Fellowship [1651825]
- BHF Intermediate Research Fellowship
- UCLH NIHR Biomedical Research Centre and Biomedical Research Unit at UCLH and Barts [FS/19/35/34374]
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This study proposes a method to obtain phase-resolved late gadolinium enhancement (LGE) images using cardiac magnetic resonance imaging. The method involves three steps and has been evaluated in phantom imaging, healthy subjects, and patients. The results demonstrate reliable imaging in the phantom and healthy subjects, while the imaging resolution and noise resilience in patients are lower compared to the reference technique. The proposed technique shows potential in integrating the advantages of phase-resolved cardiac magnetic resonance with LGE imaging, but further improvements are needed for clinical use.
Late gadolinium enhancement (LGE) with cardiac magnetic resonance (CMR) imaging is the clinical reference for assessment of myocardial scar and focal fibrosis. However, current LGE techniques are confined to imaging of a single cardiac phase, which hampers assessment of scar motility and does not allow cross-comparison between multiple phases. In this work, we investigate a three step approach to obtain cardiac phase-resolved LGE images: (1) Acquisition of cardiac phase-resolved imaging data with varying T-1 weighting. (2) Generation of semi-quantitative T-1* maps for each cardiac phase. (3) Synthetization of LGE contrast to obtain functional LGE images. The proposed method is evaluated in phantom imaging, six healthy subjects at 3T and 20 patients at 1.5T. Phantom imaging at 3T demonstrates consistent contrast throughout the cardiac cycle with a coefficient of variation of 2.55 +/- 0.42%. In-vivo results show reliable LGE contrast with thorough suppression of the myocardial tissue is healthy subjects. The contrast between blood and myocardium showed moderate variation throughout the cardiac cycle in healthy subjects (coefficient of variation 18.2 +/- 3.51%). Images were acquired at 40-60 ms and 80 ms temporal resolution, at 3T and 1.5, respectively. Functional LGE images acquired in patients with myocardial scar visualized scar tissue throughout the cardiac cycle, albeit at noticeably lower imaging resolution and noise resilience than the reference technique. The proposed technique bears the promise of integrating the advantages of phase-resolved CMR with LGE imaging, but further improvements in the acquisition quality are warranted for clinical use.
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