TY - JOUR
T1 - BUDA-MESMERISE
T2 - Rapid acquisition and unsupervised parameter estimation for T-1, T-2, M-0, B-0, and B-1 maps
AU - So, S.
AU - Park, H.W.
AU - Kim, B.
AU - Fritz, F.J.
AU - Poser, B.A.
AU - Roebroeck, A.
AU - Bilgic, B.
N1 - Funding Information:
This research was supported by the following: Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea (grant HI14C1135); the Korea Medical Device Development Fund (grant 202011B35); the MIT‐Korea ‐ KAIST Seed Fund of the MIT International Science and Technology Initiatives (MISTI); the Korea Institute of Science and Technology (grant 2E30971); the National Institutes of Health (NIH) (grants P41‐EB030006, U01‐EB026996, U01‐EB025162, R01‐EB028797, R03‐EB031175, and R01MH111444); the Dutch Science Foundation (NWO) VIDI (grants 016‐178‐052 and 14637); the European Research Council (ERC) (grants 885876 and 639938); the German Research Foundation (DFG) (grants MO 2397/5‐1, MO 2249/3–1, and MO 2397/4‐1); the German Federal Ministry of Education and Research (BMBF) (grants 01EW1711A and B); and the Forschungszentrums Medizintechnik Hamburg (FMTHH) (grant 01fmthh2017).
Funding Information:
information Bundesministerium für Bildung und Forschung, 01EW1711A; 01EW1711B; Deutsche Forschungsgemeinschaft, MO 2249/3-1; MO 2397/4-1; MO 2397/5-1; Dutch Science Foundation (NWO), 016-178-052; 14637; European Research Council (ERC), 639938; 885876; Forschungszentrums Medizintechnik Hamburg (FMTHH), 01fmthh2017; Korea Institute of Science and Technology, 2E30971; Korea Medical Device Development Fund, 202011B35; MIT-Korea - KAIST Seed Fund of the MIT International Science and Technology Initiatives (MISTI), Federal Ministry of Education and Research, Research Foundation, European Research Council, National Institutes of Health, P41-EB030006; R01-EB028797; R01MH111444; R03-EB031175; U01-EB025162; U01-EB026996; Ministry of Health, Korea Health Industry Development Institute, HI14C1135This research was supported by the following: Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea (grant HI14C1135); the Korea Medical Device Development Fund (grant 202011B35); the MIT-Korea - KAIST Seed Fund of the MIT International Science and Technology Initiatives (MISTI); the Korea Institute of Science and Technology (grant 2E30971); the National Institutes of Health (NIH) (grants P41-EB030006, U01-EB026996, U01-EB025162, R01-EB028797, R03-EB031175, and R01MH111444); the Dutch Science Foundation (NWO) VIDI (grants 016-178-052 and 14637); the European Research Council (ERC) (grants 885876 and 639938); the German Research Foundation (DFG) (grants MO 2397/5-1, MO 2249/3–1, and MO 2397/4-1); the German Federal Ministry of Education and Research (BMBF) (grants 01EW1711A and B); and the Forschungszentrums Medizintechnik Hamburg (FMTHH) (grant 01fmthh2017).
Publisher Copyright:
© 2022 International Society for Magnetic Resonance in Medicine.
PY - 2022/7
Y1 - 2022/7
N2 - Purpose Rapid acquisition scheme and parameter estimation method are proposed to acquire distortion-free spin- and stimulated-echo signals and combine the signals with a physics-driven unsupervised network to estimate T-1, T-2, and proton density (M-0) parameter maps, along with B-0 and B-1 information from the acquired signals. Theory and Methods An imaging sequence with three 90 degrees RF pulses is utilized to acquire spin- and stimulated-echo signals. We utilize blip-up/-down acquisition to eliminate geometric distortion incurred by the effects of B-0 inhomogeneity on rapid EPI acquisitions. For multislice imaging, echo-shifting is applied to utilize dead time between the second and third RF pulses to encode information from additional slice positions. To estimate parameter maps from the spin- and stimulated-echo signals with high fidelity, 2 estimation methods, analytic fitting and a novel unsupervised deep neural network method, are developed. Results The proposed acquisition provided distortion-free T-1, T-2, relative proton density (M0), B-0, and B-1 maps with high fidelity both in phantom and in vivo brain experiments. From the rapidly acquired spin- and stimulated-echo signals, analytic fitting and the network-based method were able to estimate T-1, T-2, M-0, B-0, and B-1 maps with high accuracy. Network estimates demonstrated noise robustness owing to the fact that the convolutional layers take information into account from spatially adjacent voxels. Conclusion The proposed acquisition/reconstruction technique enabled whole-brain acquisition of coregistered, distortion-free, T-1, T-2, M-0, B-0, and B-1 maps at 1 x 1 x 5 mm(3) resolution in 50 s. The proposed unsupervised neural network provided noise-robust parameter estimates from this rapid acquisition.
AB - Purpose Rapid acquisition scheme and parameter estimation method are proposed to acquire distortion-free spin- and stimulated-echo signals and combine the signals with a physics-driven unsupervised network to estimate T-1, T-2, and proton density (M-0) parameter maps, along with B-0 and B-1 information from the acquired signals. Theory and Methods An imaging sequence with three 90 degrees RF pulses is utilized to acquire spin- and stimulated-echo signals. We utilize blip-up/-down acquisition to eliminate geometric distortion incurred by the effects of B-0 inhomogeneity on rapid EPI acquisitions. For multislice imaging, echo-shifting is applied to utilize dead time between the second and third RF pulses to encode information from additional slice positions. To estimate parameter maps from the spin- and stimulated-echo signals with high fidelity, 2 estimation methods, analytic fitting and a novel unsupervised deep neural network method, are developed. Results The proposed acquisition provided distortion-free T-1, T-2, relative proton density (M0), B-0, and B-1 maps with high fidelity both in phantom and in vivo brain experiments. From the rapidly acquired spin- and stimulated-echo signals, analytic fitting and the network-based method were able to estimate T-1, T-2, M-0, B-0, and B-1 maps with high accuracy. Network estimates demonstrated noise robustness owing to the fact that the convolutional layers take information into account from spatially adjacent voxels. Conclusion The proposed acquisition/reconstruction technique enabled whole-brain acquisition of coregistered, distortion-free, T-1, T-2, M-0, B-0, and B-1 maps at 1 x 1 x 5 mm(3) resolution in 50 s. The proposed unsupervised neural network provided noise-robust parameter estimates from this rapid acquisition.
KW - distortion correction
KW - multicontrast MRI
KW - quantitative MRI
KW - stimulated echo
KW - unsupervised parameter estimation
KW - PROTON DENSITY
KW - TISSUE CHARACTERIZATION
KW - INCREASED SENSITIVITY
KW - QUANTITATIVE MRI
KW - WHITE-MATTER
KW - DOUBLE-ECHO
KW - T2
KW - T1
KW - DIFFUSION
KW - BRAIN
U2 - 10.1002/mrm.29228
DO - 10.1002/mrm.29228
M3 - Article
C2 - 35344611
SN - 0740-3194
VL - 88
SP - 292
EP - 308
JO - Magnetic Resonance in Medicine
JF - Magnetic Resonance in Medicine
IS - 1
ER -