PurposeTo develop and evaluate a cardiac phase‐resolved myocardial T1mapping sequence. MethodsThe 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 T1andestimation is performed for reconstruction of cardiac phase‐resolved T1andmaps. 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) T1mapping sequence in terms of accuracy and precision. ResultsIn phantom, TOPAZ T1values with integratedcorrection are in good agreement with spin‐echo T1values (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 T1times between the cardiac phases (analysis of variance:P = 0.14, coefficient of variation = 3.2 ± 0.8%), but underestimation compared with SAPPHIRE (T1time ± precision: 1431 ± 56 ms versus 1569 ± 65 ms). In vivo precision is comparable to SAPPHIRE T1mapping until middiastole (P > 0.07), but deteriorates in the later phases. ConclusionsThe proposed sequence allows cardiac phase‐resolved T1mapping with integratedassessment 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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Phase stabilization with motion compensated diffusion weighted imaging
Abstract PurposeDiffusion encoding gradient waveforms can impartintra‐voxelandinter‐voxeldephasing owing to bulk motion, limiting achievable signal‐to‐noise and complicating multishot acquisitions. In this study, we characterize improvements in phase consistency via gradient moment nulling of diffusion encoding waveforms. MethodsHealthy volunteers received neuro () and cardiac () MRI. Three gradient moment nulling levels were evaluated: compensation for position (), position + velocity (), and position + velocity + acceleration (). Three experiments were completed: (Exp‐1) Fixed Trigger Delay Neuro DWI; (Exp‐2) Mixed Trigger Delay Neuro DWI; and (Exp‐3) Fixed Trigger Delay Cardiac DWI. Significant differences () of the temporal phase SD between repeated acquisitions and the spatial phase gradient across a given image were assessed. Resultsmoment nulling was a reference for all measures. In Exp‐1, temporal phase SD for diffusion encoding was significantly reduced with (35% oft‐tests) and (68% oft‐tests). The spatial phase gradient was reduced in 23% oft‐tests for and 2% of cases for . In Exp‐2, temporal phase SD significantly decreased with gradient moment nulling only for (83% oft‐tests), but spatial phase gradient significantly decreased with only (50% oft‐tests). In Exp‐3, gradient moment nulling significantly reduced temporal phase SD and spatial phase gradients (100% oft‐tests), resulting in less signal attenuation and more accurate ADCs. ConclusionWe characterized gradient moment nulling phase consistency for DWI. UsingM1for neuroimaging andM1 + M2for cardiac imaging minimized temporal phase SDs and spatial phase gradients.
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- Award ID(s):
- 2205103
- PAR ID:
- 10536157
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Magnetic Resonance in Medicine
- ISSN:
- 0740-3194
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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