Blip up-down acquisition for spin- and gradient-echo imaging (BUDA-SAGE) with self-supervised denoising enables efficient T2, T2*, para- and dia-magnetic susceptibility mapping

link to paper

Blip up-down acquisition for spin- and gradient-echo imaging (BUDA-SAGE) with self-supervised denoising enables efficient T2, T2*, para- and dia-magnetic susceptibility mapping

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

Abstract

Purpose

To rapidly obtain high resolution T2, T2*, 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 T2*-, T2′-, and T2-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 T2 (=1/R2) and T2* (=1/R2*) 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 R2/R2* maps, R2′ 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 T2/T2* 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 T2/T2* mapping at 1 mm isotropic resolution under 90 s.