Cape Town - 2026 ISMRM-ISMRT Annual Meeting and Exhibition • 09-14 May 2026

Power Pitch

Diffusion Modeling To Map Tissue Microstructure

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Diffusion Modeling To Map Tissue Microstructure
Power Pitch
Diffusion
Thursday, 14 May 2026
Power Pitch Theatre 1
13:40 - 15:16
Moderators: Ricardo Coronado-Leija & Adam Phipps
Session Number: 651-02
No CME/CE Credit
This Power Pitches session highlights recent work using diffusion MRI to map tissue microstructure in the brain and body, spanning methodological developments through to translational and application-driven studies.
Skill Level: Intermediate

13:40 Figure 651-02-001.  Assessing the reproducibility of grey and white matter microstructural metrics across magnetic field and gradient strengths
Elena Grosso, Eric Bardinet, Francesca Branzoli, Stéphane Lehéricy, Mélanie Didier
Paris Brain Institute - ICM, Inserm U1127, CNRS UMR 7225, Sorbonne Université, UMR S 1127, Paris, France
Impact: We plan to investigate the variability of diffusion metrics obtained using three MRI scanners at the same site, with different gradients (80, 135 and 200 mT/m) and field strengths (3T and 7T), for use as reliable pathological biomarkers.
13:42 Figure 651-02-002.  Harmonization of NODDI parameters improves brain tumor characterization across scanners at a single site
Melanie Bauer, Stephanie Mangesius, Michaela Wagner, Johannes Kerschbaumer, Daniel Pinggera, Julian Mangesius, Astrid Grams, Elke Gizewski, Christoph Birkl
Medical University of Innsbruck, Innsbruck, Austria
Impact: Harmonization of NODDI parameters reduces scanner bias within single-site multi-scanner data, enhancing the reliability of NODDI-based biomarkers for brain tumor characterization. This improves data pooling and clinical decision-making without compromising the assessment of biological effects.
13:44 Figure 651-02-003.  SANDI diffusion imaging for brain tumor microstructure: clinical feasibility and initial histopathological validation
Giovanni Savini, Luca Cappellini, Nadia Milanesi, Francesca Geroli, Luca Raspagliesi, gaia ressa, Riccardo Levi, Alessia Lindemann, Thorsten Feiweier, DOMENICO ZACA', Matteo Battocchio, Clorindo Notte, Pietro Bontempi, Marco Riva, Federico Pessina, Letterio Politi
Humanitas University, Pieve Emanuele, Italy
Impact: SANDI enables noninvasive quantification of tumor cellularity and microstructure, potentially improving treatment response assessment and biopsy targeting. This approach establishes a pathway to evaluate tumor biology in vivo, informing surgical and therapeutic decisions.
13:46 Figure 651-02-004.  Unveiling Extra-Cellular Statistical Microstructural Information Encoded in Diffusion MRI Signals
Adam Threlfall, Yang Yang, Emiliano Spezi, Salvatore Torquato, Derek Jones, Marco Palombo, Leandro Beltrachini
Cardiff University, Cardiff, United Kingdom
Impact: This work initiates the statistical characterisation of dMRI signals, comparing the microstructural information encoded about the extended extra-cellular space, and establishing a foundation for advanced signal interpretation in isotropic tissue environments.
13:48 Figure 651-02-005.  TRACED: a novel diffusion model for characterizing extracellular diffusivity, tortuosity, and cell size and density in tumors
Joshua Marchant, Hong Hsi Lee, Elizabeth Gerstner, Susie Huang, Bruce Rosen
Massachusetts General Hospital, Boston, United States of America
Impact: TRACED provides a computationally-efficient framework for modeling time-dependent diffusion in heterogenous tissue microstructure. We demonstrate the first in vivo estimation of extracellular intrinsic diffusivity and tortuosity in a glioblastoma patient. Future work may explore the clinical applications of TRACED parameters.
13:50 Figure 651-02-006.  A fusion model of time-dependent diffusion MRI and serum biomarkers for differentiating ICC from HCC: a preliminary study
Xingqing Qin, Jin-yuan Liao, Yu-chen Wei, Yong-mei Huang, Yan-yan YU, Hui Zhang, Thorsten Feiweier, Meining Chen
The First Affiliated Hospital of Guangxi Medical University,, Nanning, China
Impact: The clinic-td-dMRI fusion model demonstrated superior diagnostic performance (AUC=0.867) in non-contrast discrimination between HCC and ICC. This approach provides detailed microstructural characterization compared to conventional DWI/IVIM techniques, thereby overcoming the inherent limitations of EOB-MRI without the requirement for contrast administration.
13:52 Figure 651-02-007.  Time-Dependent Diffusion MRI in Cervical Cancer: Noninvasive Classification and Pathologic Correlation
Wenyi Yue, Junzhong Xu, Dandan Zheng, Xiaoyu Jiang, Chaoyang Jin, Qi Yang
Beijing Chaoyang Hospital, Capital Medical University, beijing, China
Impact: Time-dependent diffusion MRI enables noninvasive microstructural assessment of cervical cancer, improving lesion subtype differentiation and pathological characterization. This approach may guide individualized treatment planning and inspire further research on tumor microenvironment imaging biomarkers.
13:54 Figure 651-02-008.  Diffusion MRI Assessment of Renal Fibrosis in Glomerulonephritis: Compartmental vs Non-Compartmental Models
JIAN LIU, Yu Wu, Daoyu Yang, Lisha Nie, Xianchun Zeng
Guizhou Provincial People’s Hospital, Guizhou, China
Impact: Integrating DKI and IVIM yields a noninvasive, standardized readout for GN fibrosis—screen early with medullary D*, stage with cortical MK. These metrics enable quantitative trial endpoints, reduce biopsy dependence, and inform timely intervention and monitoring.
13:56 Figure 651-02-009.  High-Frequency OGSE at 28.2T in a Cortical Brain Organoid and Fiber Phantom
Tatiana Nikolaeva, Maxime Yon, Maria Paula Del Popolo, Chantal Tax
University Medical Center Utrecht, Utrecht, Netherlands
Impact: High-fidelity imaging at 28.2T with strong gradients can provide a platform for validation of diffusion MRI microstructural markers.
13:58 Figure 651-02-010.  When fiber bundles are not axially symmetric: 4-dimensional fiber distributions in the human brain
Santiago Coelho, Els Fieremans, Dmitry Novikov
New York University Grossman School of Medicine, New York, United States of America
Impact: Fiber bundle orientations are characterized by 3 angles, defining orientation distributions on the 3d rotation group manifold (3-dimensional sphere)—instead of conventional distributions on a 2-dimensional sphere. We uncover such 4-dimensional distributions and bundle axial asymmetry in the human brain.
14:00 Figure 651-02-011.  Dynamic Diffusion Weighted Imaging Reveals Impaired Glymphatic Cerebrospinal Fluid Dynamics in cSVD Pathogenesis
Yurong Ma, Songhong Yue, Na Han, Mingsong Tang, Yuhui Xiong, Guangxu Han, Yanli Jiang, Pengfei Wang, Jing Zhang
Department of Magnetic Resonance, Lanzhou, China
Impact: This work establishes dynDWI as a non-invasive tool to assess glymphatic function in cSVD, providing a potential biomarker for early detection and monitoring of microstructural damage previously unattainable in clinical practice.
14:02 Figure 651-02-012.  Beyond resolution limit of in vivo axon diameter mapping with diffusion-relaxometry MRI using Multi-Echo AxCaliberSMT
Kwok-Shing Chan, Yohan Jun, Aneri Bhatt, Berkin Bilgic, Susie Huang, Hong Hsi Lee
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, United States of America
Impact: We develop a diffusion-relaxometry MRI framework that achieves comprehensive axon calibre sensitivity with a large dynamic range, allowing accurate mapping of both small and large axons in vivo and promising to improve non-invasive characterization of white matter microstructure.
14:04 Figure 651-02-013.  Characterizing heterogeneity in white matter microstructure among patients with obsessive-compulsive disorder
Shuangwei Chai, Hailong Li, Zilin Zhou, Jiaxin Jiang, Lingxiao Cao, Yuanyuan Luo, Bin Li, Xiaoqi Huang
Huaxi MR Research Center (HMRRC), Institute of Radiology and Medical Imaging, West China Hospital of Sichuan University, Chengdu, China
Impact: Our findings demonstrate that OCD is composed of neuroanatomical subtypes that have distinct microstructural alterations compared to healthy controls. Furthermore, these subtypes exhibit normalization of WM measures within sensorimotor network, fronto-limbic network and visual network, but correspond to different hemispheres.
14:06 Figure 651-02-014.  Simulating contributions of incoherent and coherent CSF motion to magnitude and phase of low-b-value diffusion-weighted MRI
Megan Martin, Zhangxuan Hu, Divya Varadarajan, Amelia Strom, Carlos Castillo-Passi, Grant Hartung, Laura Lewis, Jonathan Polimeni
Stanford University, Stanford, United States of America
Impact: Many studies assess CSF motion using parameters derived from the magnitude of dMRI data. Here we show that many forms of motion will yield the same parameter values and how the phase of the dMRI data can help distinguish them.
14:08 Figure 651-02-015.  Denoising structural connectivity matrices across a study population using random matrix theory
Bradley Karat, Sofia Nikolaidou, Zifei Ling, Jiangyang Zhang, Erika Raven, Jelle Veraart
Bernard and Irene Schwartz Center for Biomedical Imaging, Department of Radiology, New York University Grossman School of Medicine, New York, New York, United States of America
Impact: Network analyses of the brain are hindered by noise in the structural connectivity matrix. Here we propose a solution which extends contemporary denoising techniques to connectivity matrices, improving the reliability and precision of brain network analyses at the population-level.

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