Model-based T 1 mapping with sparsity constraints using single-shot inversion-recovery radial FLASH
To develop a model-based reconstruction technique for single-shot T mapping with high spatial resolution, accuracy, and precision using an inversion-recovery (IR) fast low-angle shot (FLASH) acquisition with radial encoding. The proposed model-based reconstruction jointly estimates all model paramet...
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Veröffentlicht in: | Magnetic resonance in medicine 2018-02, Vol.79 (2), p.730-740 |
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Sprache: | eng |
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Zusammenfassung: | To develop a model-based reconstruction technique for single-shot T
mapping with high spatial resolution, accuracy, and precision using an inversion-recovery (IR) fast low-angle shot (FLASH) acquisition with radial encoding.
The proposed model-based reconstruction jointly estimates all model parameters, that is, the equilibrium magnetization, steady-state magnetization, 1/ T1*, and all coil sensitivities from the data of a single-shot IR FLASH acquisition with a small golden-angle radial trajectory. Joint sparsity constraints on the parameter maps are exploited to improve the performance of the iteratively regularized Gauss-Newton method chosen for solving the nonlinear inverse problem. Validations include both a numerical and experimental T
phantom, as well as in vivo studies of the human brain and liver at 3 T.
In comparison to previous reconstruction methods for single-shot T
mapping, which are based on real-time MRI with pixel-wise fitting and a model-based approach with a predetermination of coil sensitivities, the proposed method presents with improved robustness against phase errors and numerical precision in both phantom and in vivo studies.
The comprehensive model-based reconstruction with L1 regularization offers rapid and robust T
mapping with high accuracy and precision. The method warrants accelerated computing and online implementation for extended clinical trials. Magn Reson Med 79:730-740, 2018. © 2017 International Society for Magnetic Resonance in Medicine. |
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ISSN: | 0740-3194 1522-2594 |
DOI: | 10.1002/mrm.26726 |