Optimization of IVIM-DKI MR Imaging model using Automatic Differentiation Methods: Enhancing the Computation Efficacy by 100 Fold
Motivation: Spatially constrained IDTV method have shown improved IVIM-DKI parameter estimation, although suffers from high time complexity preventing it to be used in clinical setup in real-time. Goal(s): This study aims to improve the computational time and efficiency of IVIM-DKI model optimization and proposes a novel spatially constrained IDIV-AD method using automatic differentiation framework. Approach: The proposed novel IDTV-AD method demonstrated at least 100 times faster computation time than the IDTV method maintaining the robustness and quality of parameter estimation. Results: Proposed novel IDTV-AD method demonstrated a time-efficient implementation and robust parameters estimation of IVIM-DKI parameters in pancreatic tumors and healthy pancreatic tissue. Impact: Novel spatially constrained IDTV-AD method using automatic differentiation demonstrated significantly fast (at least 100 times faster than the state-of-the-art method) and accurate IVIM-DKI parameter estimation, tested in clinical dataset of pancreatic cancer cohort.
Authors
- Raju Sharma (ORCID: https://orcid.org/0000-0001-5181-263X)
- Amit Mehndiratta (ORCID: https://orcid.org/0000-0001-6477-2462)
- Esha Baidya Kayal (ORCID: https://orcid.org/0000-0002-0377-826X)
- Kedar Khare (ORCID: https://orcid.org/0000-0002-3104-3850)
- Devasenathipathy Kandasamy (ORCID: https://orcid.org/0000-0002-8615-4937)
- M Ganeshkumar (ORCID: https://orcid.org/0000-0001-5559-6428)
- Hisham Hanif
- Himansu Maurya
- Rithvik Hariprasad
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2025-09-16
- DOI
- https://doi.org/10.58530/2025/2106
- Primary Topic
- Advanced MRI Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00