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The paper uses a cascaded spatial-temporal network to estimate tissue fractions directly from MR fingerprinting signals, skipping intermediate T1/T2 maps that can propagate errors. Reported gains over dictionary matching and pseudoinverse baselines come mainly from simulations and limited in vivo data, and the authors say clinical validation is still needed. For ML readers, the useful takeaway is the end-to-end design choice and how it is evaluated against classical pipelines.
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DeepPV-MRF: End-to-End Partial-Volume Fraction Estimation from MR Fingerprinting Time Series

arXiv2 min read

arXiv:2610.19894v1 Announce Type: cross Abstract: Background: Estimating subvoxel tissue fractions from magnetic resonance fingerprinting (MRF) is challenging. Conventional dictionary matching and segmentation pipelines can propagate errors from intermediate parametric maps into tissue fraction estimates. Purpose: We introduce DeepPV-MRF, a deep learning framework that directly estimates voxel-wise tissue fractions from raw MRF signals. Methods: A cascaded spatial-temporal network was trained on subject-derived Bloch simulations with radial k-space undersampling. The network combines temporal encoding and spatial U-Net refinement to estimate cerebrospinal fluid (CSF), gray matter (GM), and white matter (WM) fractions without intermediate T1/T2 maps. We compared DeepPV-MRF with partial-volume dictionary matching (PV-DM) and pseudoinverse estimation (PV-Pinv) using simulated and in vivo data. Results: DeepPV-MRF outperformed both methods across acquisition settings. In single-shot simulations, CSF/WM/GM mean absolute errors were 0.0418/0.0744/0.0757, versus 0.1281/0.2443/0.2958 for PV-DM and 0.2021/0.2793/0.2630 for PV-Pinv. Corresponding structural similarity values were 0.960/0.916/0.922. In vivo results showed sharper anatomical boundaries and smoother tissue transitions, while cross-shot analysis indicated improved consistency across volunteers. Conclusions: DeepPV-MRF enables accurate and efficient direct tissue fraction estimation from MRF signals, particularly with limited shots. Further validation is needed before clinical deployment.

Abstract:Background: Estimating subvoxel tissue fractions from magnetic resonance fingerprinting (MRF) is challenging. Conventional dictionary matching and segmentation pipelines can propagate errors from intermediate parametric maps into tissue fraction estimates. Purpose: We introduce DeepPV-MRF, a deep learning framework that directly estimates voxel-wise tissue fractions from raw MRF signals. Methods: A cascaded spatial-temporal network was trained on subject-derived Bloch simulations with radial k-space undersampling. The network combines temporal encoding and spatial U-Net refinement to estimate cerebrospinal fluid (CSF), gray matter (GM), and white matter (WM) fractions without intermediate T1/T2 maps. We compared DeepPV-MRF with partial-volume dictionary matching (PV-DM) and pseudoinverse estimation (PV-Pinv) using simulated and in vivo data. Results: DeepPV-MRF outperformed both methods across acquisition settings. In single-shot simulations, CSF/WM/GM mean absolute errors were 0.0418/0.0744/0.0757, versus 0.1281/0.2443/0.2958 for PV-DM and 0.2021/0.2793/0.2630 for PV-Pinv. Corresponding structural similarity values were 0.960/0.916/0.922. In vivo results showed sharper anatomical boundaries and smoother tissue transitions, while cross-shot analysis indicated improved consistency across volunteers. Conclusions: DeepPV-MRF enables accurate and efficient direct tissue fraction estimation from MRF signals, particularly with limited shots. Further validation is needed before clinical deployment.

Signal Processing (eess.SP); Artificial Intelligence (cs.AI)

arXiv:2610.19894 [eess.SP]

(or arXiv:2610.19894v1 [eess.SP] for this version)

https://doi.org/10.48550/arXiv.2610.19894 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 277 words

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