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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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Bibliographic Details
Published in:Magnetic resonance in medicine 2018-04, Vol.79 (4), p.2087-2100
Main Authors: Weingärtner, Sebastian, Shenoy, Chetan, Rieger, Benedikt, Schad, Lothar R, Schulz-Menger, Jeanette, Akçakaya, Mehmet
Format: Article
Language:English
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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.
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.26887