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

Digital Poster

Diffusion Microstructure and Beyond

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Diffusion Microstructure and Beyond
Digital Poster
Diffusion
Thursday, 14 May 2026
Digital Posters Row H
09:25 - 10:20
Session Number: 667-02
No CME/CE Credit
This session will have methods on dMRI derived microstructure

  Figure 667-02-001.  Investigating the effects of spectral anisotropy in b-tensor diffusion encoding using combined OGSE-STE waveforms at 15.2 T
Jake Hamilton, Ricardo Rios-Carrillo, Sam Laxer, Ravi Menon, Arthur Brown, Corey Baron
Robarts Research Institute - Western University, Canada
Impact: This work shows that spectral anisotropy in spherical tensor encoding has limited influence on tensor-valued metrics, but that the method used for spectral tuning between spherical and linear encoding acquisitions can impact microscopic anisotropy estimates.
  Figure 667-02-002.  Evaluating Cellular Proliferation and IDH mutation Status in Glioma Using Multiple Diffusion Models
Zhengyang Zhu, Yang Song, Huiquan Yang, Maolin Zhang, Zhiwei Zhang, Xin Zhang, Bing Zhang
Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
Impact: This study demonstrates that advanced diffusion models, particularly the tri-exponential model (TEM), can noninvasively and accurately predict key molecular markers in gliomas, offering a promising imaging biomarker approach to guide personalized treatment planning and improve patient prognosis.
  Figure 667-02-003.  Enhancing High b-value Diffusion MRI Microstructure Mapping with CASA Denoising
Mauro Zucchelli, Marco Palombo, Christos Papageorgakis, Carolyn McNabb, Derek Jones, Stefano Casagranda
Olea Medical, La Ciotat, France
Impact: Component Analysis based on Standard-deviation Attenuation (CASA) denoising can improve brain microstructure estimation obtained from diffusion MRI at high b-values, bringing brain tissue microstructure modelling closer to clinical feasibility and strengthening the link between diffusion MRI signals and neurobiological interpretation.
  Figure 667-02-004.  Diffusion MRI Reveals SF1 Overexpression–Induced Microstructural and Connectivity Changes in 3xTG Alzheimer’s Mice
Zhuoheng Liu, Jie Chen, Hongbo Wu, Xinyue Han, Nataliya Tod, Juan Liu, Nian Wang
University of Texas Southwestern Medical Center, Dallas, United States of America
Impact: Diffusion MRI reveals that SF1 overexpression partially restores microstructural integrity and long-range connectivity in 3xTg Alzheimer’s mice, particularly in auditory and motor-associated regions, suggesting NAD⁺-mediated modulation of neuroinflammation and network repair.
  Figure 667-02-005.  Assessing White Matter Damage in Mesial Temporal Lobe Epilepsy via Peak Width of Skeletonized Mean Diffusivity
Yuanyuan wei, Jinqin Li, Huiyan Zhang, Dengyan Song, Zhuo Wang, Hao Ye, Guangxu Han, Bing Chen
The First Clinical Medical College of Ningxia Medical University, Yinchuan, China
Impact: This study indicates that PSMD effectively reflects white matter damage in MRI-negative MTLE, offering a valuable imaging tool for assessment.
  Figure 667-02-006.  Kurtosis-based Imaging of Neurite and Soma Architecture (KINSA) with water exchange
Tianjia Zhu, Hao Huang
Children's Hospital of Philadelphia, Philadelphia, United States of America
Impact: We developed a KINSA model with water exchange dominantly reflected by neurite-extracellular exchange. Through water-exchange KINSA model, the kurtosis change sensitive to exchange was measured with real multi-diffusion-time marmoset dMRI data, enabling delineating the soma and neurite contributions to kurtosis.
  Figure 667-02-007.  In Vivo Axon Radius Asymmetry Mapping using Axonal Diameter Imaging (AXDI) on High Performance Gradient 3T MRI System
Ruicheng Ba, Yajing Zhang, Yuhui Xiong, Su Lui, Bing Wu
GE HealthCare MR Research, Beijing, China
Impact: Our findings establish Axonal Diameter Imaging (AXDI) for mapping hemispheric axon radius asymmetry, revealing a left-larger-than-right pattern. This provides neuroscientists a direct microstructural metric to re-evaluate white matter organization and its links to cognition, aging, and neuropsychiatric disorders.
  Figure 667-02-008.  Impact of Maximum b-Value in Q-Space Trajectory Imaging of White Matter
Oliver Gödicke, Jinyang Yu, Frederik Laun, Mark Ladd, Tristan Kuder
German Cancer Research Center (DKFZ), Heidelberg, Germany
Impact: Scaling the b-value scheme ($b_\mathrm{max}\!\in\![1250,2900]\,\mathrm{s/mm^2}$) yields modest absolute microparameter shifts and largely stable microscopic anisotropy in QTI of human white matter. This may guide pragmatic protocol design, e.g. in the presence of hardware limits.
  Figure 667-02-009.  Probing axonal loss and inflammation in a chronic stroke patient using clinical soma and neurite density imaging: case study
Dongsuk Sung, Hansol Lee, Hong Hsi Lee, Susie Huang, David Lin
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, United States of America
Impact: Clinical soma and neurite density imaging (SANDI)-derived parameters could serve as non-invasive biomarkers to characterize microstructural alterations in stroke patients on clinical scanners in 14 min, potentially useful for guiding individualized rehabilitation and monitoring treatment response.
  Figure 667-02-010.  Diffusion Complexity Mapping Enhances Visualization of Hippocampus Abnormalities in Focal Epilepsy
Antonio Carlos Senra Filho, Brunno Machado de Campos, Fernando Cendes, Andre Paschoal
University of Campinas, Campinas, Brazil
Impact: Conventional DTI metrics have poor gray matter contrast. Our novel Diffusion Complexity (DC) metric provides a high-contrast visualization of the epileptogenic hippocampus, offering a promising new biomarker to improve non-invasive analysis in focal epilepsy.
  Figure 667-02-011.  Solid-Fluid Coupling in the Brain by Mechanical and Microstructural Examination
Christoffer Olsson, Mikael Skorpil, Per Svenningsson, Rodrigo Moreno
KTH Royal Institute of Technology, Stockholm, Sweden
Impact: This study bridges diffusion and mechanical properties from MRI, enabling in vivo quantification of fluid-solid coupling in the human brain. The method opens up for new understanding of microstructural and mechanical relationships allowing probing of ECM alterations in neurological disorders.
  Figure 667-02-012.  Nonlinear Age-Related Changes in in Brain Microstructure from Middle- to Old-Age
Aziz Ulug, Christopher Filippi, Richard Watts
Cortechs Labs, Inc., San Diego, United States of America
Impact: Multi-shell diffusion imaging may reveal brain regions with accelerated decline in tissue microstructure during aging. This may be useful to detect early cognitive changes.
  Figure 667-02-013.  Quantitative mapping of brain tumour microenvironment heterogeneity with VERDICT-MRI
Matteo Figini, Samuel Rot, James Ruffle, Anestis Passalis, Bhavana Solanky, Daniel Alexander, Claudia Gandini Wheeler-Kingshott, Marco Palombo, Eleftheria Panagiotaki, Harpreet Hyare
University College London, London, United Kingdom
Impact: VERDICT-MRI could provide more specific biomarkers of brain tumour microenvironment than conventional dMRI techniques. If this is confirmed in larger groups, VERDICT could be a crucial non-invasive tool for brain tumour treatment planning and reduce the need for invasive procedures.
  Figure 667-02-014.  Relating microstructural properties of tendon and ligament to diffusion MRI metrics
Michael Focht, Advait Borole, Amir Moghaddam, Amy Wagoner Johnson, Roberto Pineda Guzman, Bruce Damon, Noel Naughton, Mariana Kersh
University of Illinois at Urbana-Champaign, Champaign, United States of America
Impact: The relationships identified in this study will improve the interpretability of DTI for clinical and computational studies of tendon structure and function.
  Figure 667-02-015.  NENSI: a new, clinically-feasible microstructure model of diffusion and relaxation in the brain tissue
Marco Pizzolato, Thina Lundsgaard Thøgersen, Mario Corral Bolaños, Tim Dyrby
Technical University of Denmark, Kgs. Lyngby, Denmark
Impact: Non-Exchanging Neurites and Somas Imaging (NENSI) enables a robust estimation of the quantities of Neurites and Somas, as well as proxies of their sizes, in the human brain on a clinical scanner using a three-shell PGSE protocol with limited assumptions.

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