Haikun Qi1, Aurelien Bustin2, Gastao Cruz2, Olivier Jaubert2, Huijun Chen3, René M Botnar4, Claudia Prieto4. 1. School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom. Electronic address: haikun.qi@kcl.ac.uk. 2. School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom. 3. Center for Biomedical Imaging Research, Department of Biomedical Engineering, Tsinghua University, Beijing, China. 4. School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom; Escuela de Ingeniería, Pontificia Universidad Católica de Chile, Santiago, Chile.
Abstract
PURPOSE: To develop a free-running framework for 3D isotropic simultaneous myocardial T1/T2 mapping and cine imaging. METHODS: Continuous data acquisition with 3D golden angle radial trajectory is used in conjunction with T2 preparation of varying echo times and inversion recovery (IR) pulses to enable simultaneous myocardial T1/T2 mapping and cine imaging. Data acquisition is retrospectively synchronized with ECG signal, and 1D respiratory self-navigation signal is extracted from the k-space center of all radial spokes. Respiratory binning is performed based on the estimated respiratory signal, enabling estimation and correction of 3D translational respiratory motion. Using high-dimensionality patch-based undersampled reconstruction with dictionary-based low-rank inversion, whole-heart T1/T2 maps and cine images can be generated with 2 mm isotropic spatial resolution. The proposed technique was validated in a standardised phantom and ten healthy subjects in comparison to conventional 2D imaging techniques. RESULTS: Phantom T1 and T2 measurements demonstrated good agreement with 2D spin echo techniques. Septal T1 estimated with the proposed technique (1185.6 ± 49.8 ms) was longer than with a conventional breath-hold 2D IR-prepared sequence (1044.3 ± 26.7 ms), whereas T2 measurements (47.6 ± 2.5 ms) were lower than a breath-hold 2D gradient spin echo sequence (52.0 ± 1.8 ms). Precision of the proposed 3D mapping was higher than conventional 2D mapping techniques. Ejection fraction measured with the proposed 3D approach (63.8 ± 6.8%) agreed well with conventional breath-held multi-slice 2D cine (62.3 ± 6.4%). CONCLUSIONS: The proposed technique provides co-registered 3D T1/T2 maps and cine images with isotropic spatial resolution from a single free-breathing scan, thereby providing a promising imaging tool for whole-heart myocardial tissue characterization and functional evaluation.
PURPOSE: To develop a free-running framework for 3D isotropic simultaneous myocardial T1/T2 mapping and cine imaging. METHODS: Continuous data acquisition with 3D golden angle radial trajectory is used in conjunction with T2 preparation of varying echo times and inversion recovery (IR) pulses to enable simultaneous myocardial T1/T2 mapping and cine imaging. Data acquisition is retrospectively synchronized with ECG signal, and 1D respiratory self-navigation signal is extracted from the k-space center of all radial spokes. Respiratory binning is performed based on the estimated respiratory signal, enabling estimation and correction of 3D translational respiratory motion. Using high-dimensionality patch-based undersampled reconstruction with dictionary-based low-rank inversion, whole-heart T1/T2 maps and cine images can be generated with 2 mm isotropic spatial resolution. The proposed technique was validated in a standardised phantom and ten healthy subjects in comparison to conventional 2D imaging techniques. RESULTS: Phantom T1 and T2 measurements demonstrated good agreement with 2D spin echo techniques. Septal T1 estimated with the proposed technique (1185.6 ± 49.8 ms) was longer than with a conventional breath-hold 2D IR-prepared sequence (1044.3 ± 26.7 ms), whereas T2 measurements (47.6 ± 2.5 ms) were lower than a breath-hold 2D gradient spin echo sequence (52.0 ± 1.8 ms). Precision of the proposed 3D mapping was higher than conventional 2D mapping techniques. Ejection fraction measured with the proposed 3D approach (63.8 ± 6.8%) agreed well with conventional breath-held multi-slice 2D cine (62.3 ± 6.4%). CONCLUSIONS: The proposed technique provides co-registered 3D T1/T2 maps and cine images with isotropic spatial resolution from a single free-breathing scan, thereby providing a promising imaging tool for whole-heart myocardial tissue characterization and functional evaluation.
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