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Blip up-down acquisition for spin- and gradient-echo imaging (BUDA-SAGE) with self-supervised denoising enables efficient T-2, T-2, para- and dia-magnetic susceptibility mapping

Cited 13 time in Web of Science Cited 14 time in Scopus
Authors

Zhang, Zijing; Cho, Jaejin; Wang, Long; Liao, Congyu; Shin, Hyeong-Geol; Cao, Xiaozhi; Lee, Jongho; Xu, Jinmin; Zhang, Tao; Ye, Huihui; Setsompop, Kawin; Liu, Huafeng; Bilgic, Berkin

Issue Date
2022-08
Publisher
John Wiley & Sons Inc.
Citation
Magnetic Resonance in Medicine, Vol.88 No.2, pp.633-650
Abstract
Purpose To rapidly obtain high resolution T-2, T-2*, and quantitative susceptibility mapping (QSM) source separation maps with whole-brain coverage and high geometric fidelity. Methods We propose Blip Up-Down Acquisition for Spin And Gradient Echo imaging (BUDA-SAGE), an efficient EPI sequence for quantitative mapping. The acquisition includes multiple T-2*-, T-2 '-, and T-2-weighted contrasts. We alternate the phase-encoding polarities across the interleaved shots in this multi-shot navigator-free acquisition. A field map estimated from interim reconstructions was incorporated into the joint multi-shot EPI reconstruction with a structured low rank constraint to eliminate distortion. A self-supervised neural network (NN), MR-Self2Self (MR-S2S), was used to perform denoising to boost SNR. Using Slider encoding allowed us to reach 1 mm isotropic resolution by performing super-resolution reconstruction on volumes acquired with 2 mm slice thickness. Quantitative T-2 (=1/R-2) and T-2* (=1/R-2*) maps were obtained using Bloch dictionary matching on the reconstructed echoes. QSM was estimated using nonlinear dipole inversion on the gradient echoes. Starting from the estimated R-2/R-2* maps, R-2 ' information was derived and used in source separation QSM reconstruction, which provided additional para- and dia-magnetic susceptibility maps. Results In vivo results demonstrate the ability of BUDA-SAGE to provide whole-brain, distortion-free, high-resolution, multi-contrast images and quantitative T-2/T-2* maps, as well as yielding para- and dia-magnetic susceptibility maps. Estimated quantitative maps showed comparable values to conventional mapping methods in phantom and in vivo measurements. Conclusion BUDA-SAGE acquisition with self-supervised denoising and Slider encoding enables rapid, distortion-free, whole-brain T-2/T-2* mapping at 1 mm isotropic resolution under 90 s.
ISSN
0740-3194
URI
https://hdl.handle.net/10371/185939
DOI
https://doi.org/10.1002/mrm.29219
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