PRIME-SVR is presented, the first implicit neural representation (INR) framework for joint HR reconstruction from multi-echo MRI, which improves reconstruction sharpness, anatomical accuracy, and cross-TE structural consistency by 14%, and accelerates quantitative imaging by reducing the data needed for multi-TE reconstruction.
Abstract
Slice-to-volume reconstruction (SVR) is the standard method for obtaining high-resolution (HR) 3D fetal brain volumes from motion-corrupted 2D MRI slice stacks acquired in multiple orientations. Existing SVR methods are optimized and validated only for clinical-range echo times (TEs), limiting their use at non-clinical TEs and making them incompatible with quantitative T2 mapping, a protocol- and center-independent biomarker of fetal brain maturation requiring HR reconstructions across multiple TEs. We present PRIME-SVR, the first implicit neural representation (INR) framework for joint HR reconstruction from multi-echo MRI. A single fully connected network models a continuous function from spatial coordinates to signal intensities across TEs, while a second network estimates slice-specific acquisition degradations. Cross-TE coherence is enforced via a Bloch equation-derived regularization penalizing deviations from expected T2 decay, with adaptive weighting that strengthens coupling for degraded stacks. The method is fully self-supervised. We validate PRIME-SVR on 39 in vivo fetal acquisitions (13 subjects x 3 TEs) from two centers, two vendors, and two field strengths (1.5 T and 0.55 T). Compared to state-of-the-art SVR, PRIME-SVR improves reconstruction sharpness by 47%, anatomical accuracy by 30%, and cross-TE structural consistency by 14%. It enables reconstruction at late TEs previously inaccessible to SVR, yielding the first 0.8 mm isotropic T2 maps at 0.55 T and the first T2 maps derived from INR-based SVR. PRIME-SVR also accelerates quantitative imaging by reducing the data needed for multi-TE reconstruction, cutting acquisition from 15 to 10 minutes while keeping T2 accuracy within 1.7% in white and deep gray matter, or to 5 minutes with a mean T2 error of 2.3% for high-quality acquisitions.
To extend localized quadratic (LQ) RF encoded spin‐echo imaging with acquisition and reconstruction strategies that improve efficiency and artifact robustness, positioning it as a practical alternative to 3D FSE for high‐resolution volumetric brain MRI.
Guruprasad Krishnamoorthy, J. Velikina, James G Pipe· Magnetic Resonance in Medici...· 0 citations
AGW-PBR improves brain MRI SR while preserving tissue-transition information relevant to downstream analysis and support tissue-mixture entropy as an effective supervision signal for partial-volume-aware MRI reconstruction.
Xiaoli Tong, Wen-Yun Yang, Zi-Heng Zhang et al.· 0 citations
Deep Resolve improved the robustness of automated brain segmentation in accelerated T2-weighted MRI, reducing cross-protocol variability and improving spatial reproducibility, with the largest reduction in reference-relative error in the most acceleration-sensitive pipeline.
J. Lasek, R. Obuchowicz, M. Strzelecki et al.· medRxiv· 0 citations
VIPP-SR (View-Independent Patched Projection Super-Resolution), a cross-contrast guided super-resolution framework that restores the inter-plane resolution of an existing anisotropic T2w volume without an isotropic ground-truth T2w, is proposed.
M. Shen, Haicheng Wang, Meghna Trivedi et al.· 0 citations
CineDiff enabled high-quality reconstruction of highly accelerated 2D RT cine CMR and reduced block-like artifacts and preserved finer anatomical detail compared with traditional compressed sensing and a variational network method, termed CineVN.
Xuan Lei, Philip Schniter, Juliet Varghese et al.· 0 citations
SL-MOLED provides accurate, repeatable, and artifact-robust quantitative mapping within a substantially reduced acquisition time, offering a promising framework for reliable multi-parametric MRI with potential for clinical translation.
Wei-Kun Chen, Qing Lin, Tai-Shan Kang et al.· Physics in Medicine and Biol...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.