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Rapid whole brain motion-robust mesoscale in-vivo MR imaging using multi-scale implicit neural representation.

Authors

Lyu J,Ning L,Consagra W,Liu Q,Rushmore RJ,Bilgic B,Rathi Y

Affiliations (5)

  • Mass General Brigham, Harvard Medical School, MA, United States. Electronic address: [email protected].
  • Mass General Brigham, Harvard Medical School, MA, United States.
  • Department of Statistics, University of South Carolina, SC, United States.
  • Department of Anatomy and Neurobiology, Boston University Chobanian & Avedisian School of Medicine, MA, United States.
  • Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, MA, United States; Department of Radiology, Harvard Medical School, MA, United States; Harvard/MIT Health Sciences and Technology, MA, United States.

Abstract

High-resolution whole-brain in vivo MR imaging at mesoscale resolutions remains challenging due to long scan durations, motion artifacts, and limited signal-to-noise ratio (SNR). While acquiring multiple anisotropic scans from rotated slice orientations offers a practical compromise, reconstructing accurate isotropic volumes from such inputs remains non-trivial due to the lack of high-resolution ground truth and the presence of inter-scan motion. To address these challenges, we proposes Rotating-view super-resolution (ROVER)-MRI, an unsupervised framework based on multi-scale implicit neural representations (INR), enabling accurate recovery of fine anatomical details from multi-view thick-slice acquisitions. ROVER-MRI employs coordinate-based neural networks to implicitly and continuously encode image structures at multiple spatial scales, simultaneously modeling anatomical continuity and correcting inter-view motion through an integrated registration mechanism. Validation on ex-vivo monkey brain data and multiple in-vivo human datasets demonstrates substantially improved reconstruction performance compared to bi-cubic interpolation and state-of-the-art regularized least-squares super-resolution reconstruction (LS-SRR) with 2-fold reduction in scan time. Notably, ROVER-MRI enables whole-brain in-vivo T2-weighted imaging at 180μm isotropic resolution in just 17 min on a 7T scanner, achieving a 22.4% reduction in relative error compared to LS-SRR. We also demonstrate improved SNR using ROVER-MRI compared to a time-matched 3D GRE acquisition. Quantitative results on several datasets demonstrate better sharpness of the reconstructed images with ROVER-MRI for different super-resolution factors (5 to 11). These findings highlight ROVER-MRI's potential as a rapid, accurate, and motion-resilient mesoscale imaging solution, promising substantial advantages for neuroimaging studies.

Topics

Journal Article

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