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PRIME-SVR: Physics-infoRmed Implicit Multi-Echo Slice-to-Volume Reconstruction for Fetal T2 mapping

Authors

Do you know Busra Bulut?You can claim authorship or link another user.Do you know Maik Dannecker?You can claim authorship or link another user.Do you know Thomas Sanchez?You can claim authorship or link another user.Do you know Sara Neves Silva?You can claim authorship or link another user.Do you know Steven Jia?You can claim authorship or link another user.Do you know Jean-Baptiste Ledoux?You can claim authorship or link another user.Do you know Leo Pomar?You can claim authorship or link another user.Do you know Joanna Sichitiu?You can claim authorship or link another user.Do you know Yvan Gomez?You can claim authorship or link another user.Do you know Meriam Koob?You can claim authorship or link another user.Do you know Vincent Dunet?You can claim authorship or link another user.Do you know Maria Deprez?You can claim authorship or link another user.Do you know Guillaume Auzias?You can claim authorship or link another user.Do you know Francois Rousseau?You can claim authorship or link another user.Do you know Jana Hutter?You can claim authorship or link another user.Do you know Daniel Rueckert?You can claim authorship or link another user.Do you know Meritxell Bach Cuadra?You can claim authorship or link another user.

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.

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