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

Digital Poster

Non-Proton MRI: Methods and Applications

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Non-Proton MRI: Methods and Applications
Digital Poster
Contrast Mechanisms
Tuesday, 12 May 2026
Digital Posters Row J
16:00 - 16:55
Session Number: 469-05
No CME/CE Credit
This session presents emerging clinical and preclinical applications of non-proton MRI.

  Figure 469-05-001.  Impact of Skin Barrier Function on Skin Sodium Quantification with 23Na MRI at 7T
Aditya Jhajharia, Jie Zhu, Zanib Naeem, Katrina Abuabara, Michael Ohliger, An Vu, Jeremy Gordon
University Of California, San Francisco (UCSF), United States of America
Impact: This study establishes the repeatability and reliability of sodium (23Na) MRI for skin sodium quantification and demonstrates its capability to detect changes associated with skin barrier function, providing a foundation for non-invasive assessment of disease-related alterations.
  Figure 469-05-002.  Open-source implementation and validation of the 3D CRISTINA sodium MQC sequence
Valentin Jost, Dominik Zehender, Frank Zoellner
Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany
Impact: Releasing a Pulseq-based 3D-CRISTINA sodium multi-coherence imaging implementation enables reliable simultaneous single and triple quantum imaging across various scanner platforms, supporting cross-site validation and technological innovation in sodium MRI, thereby accelerating development of quantitative biomarkers of cellular viability.
  Figure 469-05-003.  Variability in 13C MRS measurement of Leg Glycogen in Children.
Abi Spicer, Elizabeth Simpson, Ian Macdonald, Penny Gowland, Stephen Bawden
University of Nottingham, Nottingham, United Kingdom
Impact: With both intra-subject and inter-subject reproducibility of leg skeletal muscle glycogen (LMGly) measures in children matching literature values for adults, this shows the viability of MRS as a tool to measure LMGly in a diverse populations.
  Figure 469-05-004.  Sub-Millimolar in vivo 1H/19F MRI Boosted by a Metamaterial Enhancer and Advanced Denoising
Teng Gong, Anfeng Li, Shuangchen Li, Lele Ma, Pingsheng Huang, Zhong-Xing Jiang, Xiaolei Song
Tsinghua University, Beijing, China
Impact: We enabled sub-millimolar in vivo 19F-MRI of a fluorinated nanoprobe, by integrating metamaterial enhancers, sequence optimization and BM3D denoising. The significant improvement of sensitivity (>5 folds) could facilitate the application of 19F-MRI cell tracking and cancer therapy monitoring.
  Figure 469-05-005.  Reproducibility Analysis of brain and calf muscle energy metabolism using 31P MRS at 3.0T
Mengyuan Xu, Jin Cai, Baiyan Jiang, Yinghui Ge, Zhiping Guo
Fuwai Central China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, China
Impact: This study demonstrates high test-retest repeatability of ³¹P-MRS for quantifying phosphate metabolism in the brain and calf muscle at 3T, supporting its use in longitudinal clinical studies for monitoring disease progression and treatment response.
  Figure 469-05-006.  Reference-Free Intensity Correction for 7T ²³Na MRI: A Comparative Study
Yuancheng Jiang, Jianxun Qu, Armin NAGEL, Caohui Duan
MR Research Collaboration, Siemens Healthineers Ltd., Beijing, China
Impact: This work provides a guideline for selecting an optimal reference-free intensity correction method for 7T ²³Na MRI. By enabling accurate quantification without extra scan time, our findings can accelerate the clinical translation of quantitative ²³Na MRI in neurological disorders.
  Figure 469-05-007.  ¹³C-lactate imaging without hyperpolarization using Selective Polarization Transfer (SPT) / NOE CSI-SSFP experiments
Elton Montrazi, Lucio Frydman
Weizmann Institute, Rehovot, Israel
Impact: Our results demonstrate that ¹³C-lactate can be detected in tumors by tracking injected ¹³C-glucose, without hyperpolarization, using SPT/NOE-CSI-SSFP experiments that enhance the SNR by a factor of 2–3 compared with conventional SSFP.
  Figure 469-05-008.  7T 31P MT-ISIS for Quantifying CK and ATPase in Human Skeletal Muscle
Ying-Hua Chu, Caixia Fu, Wenwen Yu, He Wang, Yi-Cheng Hsu
MR Research Collaboration Team, Shanghai, China
Impact: A 7T 31P magnetization transfer (MT-ISIS) protocol quantifies PCr↔ATP (CK) and Pi→ATP (ATPase) in ~5 minutes, yielding T₁ and exchange rates consistent with prior literature and robust to flip angle errors.
  Figure 469-05-009.  Subject-Specific Voxel Model for Assessing the Impact of B1- Correction on aTSC in Quantitative 23Na MRI at 7T
Jana Losch, Thomas Fiedler, Anna Scheipers, Armin NAGEL, Mark Ladd, Tanja Platt
German Cancer Research Center (DKFZ), Heidelberg, Germany
Impact: When simulating B1- for inhomogeneity corrections in quantitative ²³Na MRI, generic voxel models may suffice for reliable organ-specific aTSC estimation. This is encouraging, as using readily available models avoids complex personalized modelling, thus supporting wider adoption of quantitative sodium MRI.
  Figure 469-05-010.  Multicolor 19F MRI using Spectral Hadamard-Encoding
Kian Tadjalli Mehr, Felix Spreter, Simon Reiss, Johannes Fischer, Ali Özen, Natalie Hoppe, Gunjan Arya, Alexander Maier, Michael Bock
University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Impact: For Multicolor 19F MRI Hadamard-encoding is a simple alternative to selective refocusing or deconvolution methods, which can efficiently differentiate an arbitrary number of resonances, making it a powerful tool in combination with spectral fitting.
  Figure 469-05-011.  A Homogeneous Perfluorocarbon Phantom for Quantitative 19F MRI of Large Animals
Kian Tadjalli Mehr, Ali Özen, Felix Spreter, David Boll, Simon Reiss, Lisa Regler, Johannes Fischer, Alexander Maier, Michael Bock
University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Impact: The affordable, homogeneous 19F phantom enables accurate sensitivity mapping of 19F coils, supporting coil development and quality assurance of the imaging hardware.
  Figure 469-05-012.  Open-source Bloch–Siegert and Double Flip Angle B₁ mapping for sodium MRI with optional TV-accelerated reconstruction
Valentin Jost, Dominik Zehender, Safa Özdemir, Frank Zoellner
Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany
Impact: We propose two Pulseq sequences with high undersampling for sodium B1 mapping. Implemented within an open source framework, they allow for reproducible and compatible results, therefore, facilitating broader access to quantitative sodium MRI.
  Figure 469-05-013.  Orientation Dependence of the 1H Solid-State NMR Spectrum and T1Ds at the Myelin/Water Interface
Cariad Knight, Alex Ensworth, Cornelia Laule, Alex MacKay, Carl Michal
University of British Columbia, Vancouver, Canada
Impact: Directly probes the myelin membrane-water interface, resolving orientation-specific 1H features that link solid-state NMR approaches to T1D/ihMT mechanisms. Understanding myelin membrane organization and dynamics can improve design and interpretation of myelin-sensitive MRI and strengthen validation of demyelination biomarkers in vivo.
  Figure 469-05-014.  In vivo high-resolution phosphorus metabolite mapping using a novel multi-resolution approach for 31P MRSI at 7 Tesla
Jan-Philipp Schmitz, Justyna Platek, Bela Seng, Peter Bachert, Mark Ladd, Andreas Korzowski, Vanessa Franke
German Cancer Research Center (DKFZ), Heidelberg, Germany
Impact: To advance the research and clinical applicability of ³¹P MRSI, we demonstrate the utility of multi-resolution quantification in vivo. We validate its ability to improve quantification robustness for low-SNR metabolites and enable reliable extracellular pH mapping in accelerated acquisitions.
  Figure 469-05-015.  Modelling Stimulated Echoes in Single Shot Fixed Sodium Reconstruction for TQ/SQ correction
Dominik Zehender, Valentin Jost, Lothar Schad, Frank Zoellner
Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany
Impact: Using a Lorentzian model for the fixed TQTPPI wo180 reconstruction we are able to extract $T^*_{2s/f}$ despite stimulated echoes. This will potentially enable the correction of the sodium TQ-signal to the optimal evolution time when not measured at $t_{evo}=t_{opt}$.
  Figure 469-05-016.  A Birdcage Any-nucleus Distributed Active Programmable Transmit (ADAPT) Coil
Jóan Hofgaard Køtlum, Michiel Esvelt, Ingmar Voogt, Busra Kahraman, Mark Gosselink, Vitaliy Zhurbenko, Dennis Klomp, Jan Ardenkjaer-Larsen, Victor Han
Technical University of Denmark, Kgs. Lyngby, Denmark
Impact: We present a pathway towards an any-nucleus transmit coil that could replace traditional MRI body coils. This would enable routine X-nuclei imaging and spectroscopy by simply changing receive coils for different nuclei, providing information for early diagnosis and treatment evaluation.

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