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Temporally resolved parametric assessment of Z-magnetization recovery (TOPAZ): Dynamic myocardial T 1 mapping using a cine steady-state look-locker approach
To develop and evaluate a cardiac phase-resolved myocardial T mapping sequence. The proposed method for temporally resolved parametric assessment of Z-magnetization recovery (TOPAZ) is based on contiguous fast low-angle shot imaging readout after magnetization inversion from the pulsed steady state....
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Published in: | Magnetic resonance in medicine 2018-04, Vol.79 (4), p.2087-2100 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | To develop and evaluate a cardiac phase-resolved myocardial T
mapping sequence.
The proposed method for temporally resolved parametric assessment of Z-magnetization recovery (TOPAZ) is based on contiguous fast low-angle shot imaging readout after magnetization inversion from the pulsed steady state. Thereby, segmented k-space data are acquired over multiple heartbeats, before reaching steady state. This results in sampling of the inversion-recovery curve for each heart phase at multiple points separated by an R-R interval. Joint T
and B1+ estimation is performed for reconstruction of cardiac phase-resolved T
and B1+ maps. Sequence parameters are optimized using numerical simulations. Phantom and in vivo imaging are performed to compare the proposed sequence to a spin-echo reference and saturation pulse prepared heart rate-independent inversion-recovery (SAPPHIRE) T
mapping sequence in terms of accuracy and precision.
In phantom, TOPAZ T
values with integrated B1+ correction are in good agreement with spin-echo T
values (normalized root mean square error = 4.2%) and consistent across the cardiac cycle (coefficient of variation = 1.4 ± 0.78%) and different heart rates (coefficient of variation = 1.2 ± 1.9%). In vivo imaging shows no significant difference in TOPAZ T
times between the cardiac phases (analysis of variance: P = 0.14, coefficient of variation = 3.2 ± 0.8%), but underestimation compared with SAPPHIRE (T
time ± precision: 1431 ± 56 ms versus 1569 ± 65 ms). In vivo precision is comparable to SAPPHIRE T
mapping until middiastole (P > 0.07), but deteriorates in the later phases.
The proposed sequence allows cardiac phase-resolved T
mapping with integrated B1+ assessment at a temporal resolution of 40 ms. Magn Reson Med 79:2087-2100, 2018. © 2017 International Society for Magnetic Resonance in Medicine. |
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ISSN: | 0740-3194 1522-2594 |
DOI: | 10.1002/mrm.26887 |