Key result
Rosette cardiac MR fingerprinting enabled simultaneous quantification of myocardial T1, T2, and proton density fat fraction, yielding significantly higher T1 values (1081.1 ms) compared to spiral cMRF (1002 ms).
Why the study?
The study aimed to extend cardiac MR Fingerprinting using rosette k-space trajectories to allow simultaneous myocardial T1, T2, and proton density fat fraction mapping.
Absolute Event Rate: 1081.1% vs 1002%
p-value: p=<0.05
Rosette cMRF enables efficient simultaneous quantification of myocardial T1, T2, and PDFF, with potential for improved tissue characterization through effective fat suppression.
Supports feasibility of simultaneous cardiac T1/T2/PDFF mapping; leaves open validation before clinical adoption.
The goal of this work is to extend prior work on cardiac MR Fingerprinting (cMRF) using rosette k-space trajectories to enable simultaneous T 1 , T 2 , and proton density fat fraction (PDFF) mapping in the heart. A rosette trajectory designed for water-fat separation at 1.5T was used in a 2D ECG-triggered 15-heartbeat cMRF sequence. Water and fat specific T 1 and T 2 maps were generated from the cMRF data. A PDFF map was also retrieved using Hierarchical IDEAL by segmenting the rosette cMRF data into multiple echoes. The accuracy of rosette cMRF in T 1 , T 2 , and PDFF quantification was validated in the ISMRM/NIST phantom and an in-house built fat fraction phantom, respectively. The proposed method was also applied for myocardial tissue mapping of healthy subjects and cardiac patients at 1.5T. T 1 , T 2 , and PDFF values measured using rosette cMRF in the ISMRM/NIST phantom and the fat fraction phantom agreed well with the reference values. In 16 healthy subjects, rosette cMRF yielded T 1 values which were 80~90 ms higher than spiral cMRF and MOLLI. T 2 values obtained using rosette cMRF were ~3 ms higher than spiral cMRF and ~5 ms lower than conventional T 2 -prep bSSFP method. Rosette cMRF was also able to detect abnormal T 1 and T 2 values in cardiomyopathy patients and may provide more accurate maps due to effective fat suppression. In conclusion, this study shows that rosette cMRF has the potential for efficient cardiac tissue characterization through simultaneous quantification of myocardial T 1 , T 2 , and PDFF.
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Liu et al. (2022) studied Healthy and suspected cardiomyopathy (n=18). Rosette cardiac MR Fingerprinting (cMRF) vs. Spiral cMRF and conventional mapping was evaluated on Myocardial T1 relaxation time (ms) (p=<0.05). Rosette cardiac MR fingerprinting enabled simultaneous quantification of myocardial T1, T2, and proton density fat fraction, yielding significantly higher T1 values (1081.1 ms) compared to spiral cMRF (1002 ms).
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