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

Digital Poster

Hyperpolarization: Novel Applications

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Hyperpolarization: Novel Applications
Digital Poster
Contrast Mechanisms
Tuesday, 12 May 2026
Digital Posters Row F
08:20 - 09:15
Session Number: 465-01
No CME/CE Credit
For researchers and clinicians interested in the latest advances of hyperpolarization

  Figure 465-01-001.  Evidence of compartmentalized redox equilibria in hyperpolarized 13C MRI of the brain
Dylan Dingwell, Biranavan Uthayakumar, Nicole Cappelletto, Albert Chen, Hany Soliman, Charles Cunningham
University of Toronto, Toronto, Canada
Impact: Modelling of human hyperpolarized 13C MRI reproduced in vivo evidence of lactate oxidation using a multi-compartment model, clarifying the importance of compartment-specific redox dynamics and facilitating further investigation of mitochondrial lactate consumption and intercellular monocarboxylate shuttling using 13C MRI.
  Figure 465-01-002.  Probing intratumoral metabolic compartmentalisation in FHd-RCC using clinical HP 13C-MRI and MSI
Ines Horvat-Menih, Ruth Casey, James Denholm, Gregory Hamm, Heather Hulme, John Gallon, Alixander Khan, Joshua Kaggie, Andrew Gill, Andrew Priest, Joao Duarte, Cissy Yong, Cara Brodie, James Whitworth, Simon Barry, Richard Goodwin, Shubha Anand, Marc Dodd, Katherine Honan, Sarah Welsh, Anne Warren, Tevita Aho, Grant Stewart, Thomas Mitchell, Mary McLean, Ferdia Gallagher
University of Cambridge, Cambridge, United Kingdom
Impact: HP 13C-MRI may be a promising technique to characterise FHd-RCC. This could guide biopsies to regions of highest metabolic dysregulation to obtain the tumour samples of greatest clinical significance, which in turn can guide treatment decisions and inform response.
  Figure 465-01-003.  Accelerating hyperpolarized 13C urea brain perfusion imaging using L+S reconstruction with dual-tree wavelet regularization
Minjie Zhu, Yaewon Kim, Dan Vigneron, Jeremy Gordon
University Of California, San Francisco (UCSF), United States of America
Impact: The proposed reconstruction method enables a threefold acceleration in 13C urea perfusion imaging without introducing significant artifacts, thereby enhancing temporal resolution and improving the quantification of cerebral blood flow.
  Figure 465-01-004.  UV-induced hyperpolarization for in vivo 13C-MRI in awake mice: comparison with the trityl radical method
Maiko Ono, Andrea Capozzi, Kosei Hirata, Chikara Yamauchi, Keita Saito, Mor Mishkovsky, Yuhei Takado
National Institutes for Quantum Science and Technology, Chiba, Japan
Impact: This study highlights the biological applicability of UV-induced hyperpolarized [1-13C]D-pyruvate. Using MRSI, we detected early hippocampal metabolic alterations in an Alzheimer’s disease mouse model, supporting its potential as a translational tool for probing metabolic pathology in neurodegenerative diseases.
  Figure 465-01-005.  Comparative evaluation of hyperpolarized [13C]pyruvate and [13C]lactate for imaging neuronal and glioma metabolism
Jun Chen, Jaideep Chaudhary, Zohreh Erfani, Sarah Al Nemri, Erik Plautz, Erin Seeley, Xiaodong Wen, Brenda Bartnik-Olson, Ian Corbin, Jae Hong Park
University of Texas Southwestern Medical Center, Dallas, United States of America
Impact: This work presents the relative strengths of hyperpolarized pyruvate and lactate as neurometabolic imaging agents, establishing guidelines for interpreting cerebral products of hyperpolarized lactate and pyruvate and for assessing neuronal and glioma metabolism in vivo.
  Figure 465-01-006.  Pharmacokinetic Modeling with a Convolutional Neural Network of Hyperpolarized 13C-Pyruvate MRI Metabolism in the Human Heart
Mario Quicana, Anna Bennett Haller, Dillon Yeh, Sule Sahin, Nikhil Deveshwar, Avantika Sinha, Peder Larson
University of California at Berkeley, berkeley, United States of America
Impact: This digital phantom-based framework enables training and validation of deep learning models for quantification of cardiac metabolism with hyperpolarized 13C-pyruvate MRI. These models can integrate spatial and kinetic information for more robust maps of metabolism.
  Figure 465-01-007.  SABRE-Hyperpolarized [1-13C]ketoisocaproate-d2 Allows Profiling of Branched-Chain-Amino-Acid Transferase in vitro and in vivo
Stefan Petersen, Philipp Groß, Paul Schmidt, Henri de Maissin, Robert Willing, Adriana Sacristán-Martín, Lisa Heß, Sebastian Lucas, Maxim Zaitsev, Dominik von Elverfeldt, Martin Grashei, Franz Schilling, Max von Delius, Thomas Reinheckel, Andreas Schmidt
University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Impact: This work establishes SLIC-SABRE-hyperpolarized [1-¹³C]ketoisocaproate-d2 as a rapid, cost-effective approach to probe branched-chain-amino-acid metabolism, enabling metabolic phenotyping of breast cancer and expanding the repertoire of parahydrogen-based hyperpolarized ¹³C agents for biomedical MRI
  Figure 465-01-008.  An integrated HP [¹³C,¹⁵N₂]Urea + [1-¹³C]Pyruvate MRI Approach for Measuring Human BBB Integrity and Cerebral Metabolism
Yaewon Kim, Hsin-Yu Chen, Minjie Zhu, Duy Dang, James Slater, Charlie Wang, Jeremy Gordon, Chris Suszczynski, Sri Maddali, Adam Gaunt, Rui Chen, Javier Villanueva-Meyer, Duan Xu, Peder Larson, Robert Bok, Susan Chang, Dan Vigneron
University Of California, San Francisco (UCSF), United States of America
Impact: 
This study demonstrated the feasibility of combining hyperpolarized [13C,15N2]urea and [1-13C]pyruvate MRI to probe cerebral perfusion and metabolism, enabling new opportunities for noninvasive assessment of blood–brain barrier integrity and neurovascular dysfunction in neurological diseases.
  Figure 465-01-009.  Extraction of the vascular component of 13C-pyruvate signal: correlation with ASL
Biranavan Uthayakumar, Dylan Dingwell, Nicole Cappelletto, Albert Chen, Nathan Ma, Chris Heyn, Hany Soliman, Charles Cunningham
University of Toronto, Toronto, Canada
Impact: Kinetic modelling of hyperpolarized [1-13C]-pyruvate MRI enabled regional CBF estimation, yielding more physiologically meaningful perfusion measures compared to unmodeled signals. However, weak correlations with arterial spin labelling CBF suggest that additional physiological factors influence the distribution of [1-13C]- pyruvate distribution.
  Figure 465-01-010.  The 13C-metabolite profile of white matter hyperintensities measured with hyperpolarized 13C-pyruvate MRI
Nicole Cappelletto, Hany Soliman, Biranavan Uthayakumar, Arjun Sahgal, Albert Chen, Ruby Endre, Nathan Ma, William Perks, Chris Heyn, Charles Cunningham
University of Toronto, Toronto, Canada
Impact: Hyperpolarized 13C-pyruvate MRI reveals decreased 13C-metabolism in white matter hyperintensities and may aid in understanding their underlying pathophysiology, etiology, and developmental phases. To our knowledge, this is the first report of hyperpolarized 13C MRI signals measured in white matter hyperintensities.
  Figure 465-01-011.  Hyperpolarized ¹³C-pyruvate first-pass metabolism reflects the first-pass perfusion pattern observed with [¹⁵O]H₂O PET/CT
Niels Jespersen, Esben Hansen, Steen Joergensen, Christoffer Laustsen, Henrik Wiggers, Lars Gormsen, Lotte Bonde Bertelsen, Rasmus Tougaard
Aarhus University, Aarhus, Denmark
Impact: The strong correlations between hyperpolarized MRSI metabolites and PET-derived myocardial blood flow supports the potential of hyperpolarized cardiac MRSI in ischemic heart disease. This opens new avenues for novel insights into cardiac substrate use, viability assessment, and metabolic remodeling.
  Figure 465-01-012.  Exercise-Induced Modulation of Myocardial Substrate Utilization Measured with Hyperpolarized [1-¹³C] Pyruvate CMR
Avantika Sinha, Anna Bennett Haller, Minjie Zhu, Adam Gaunt, Donghyun Hong, Irvane Kamga, Erin Argentieri, Michael Salerno, Moriel Vandsburger, Roselle Abraham, Peder Larson
University Of California, San Francisco (UCSF), United States of America
Impact: We demonstrate the feasibility of HP ¹³C-pyruvate MRI to capture acute metabolic changes in the left-ventricular myocardium using low to moderate lower-limb exercise in the scanner. Our results showed increased lactate and bicarbonate production after exercise in a fasted state.

  Figure 465-01-013.  1H PRESS Detection of Hepatic Lactate at 3T and Correlation with Hyperpolarized 13C MRI
Wen Yen Chai, Ching-Yi Hsieh, Cheng-En Hsieh, Ying-Chieh Lai, Gigin Lin
Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan
Impact: This study demonstrates that long-TE $^1$H PRESS at 3 T can reliably detect hepatic lactate and correlates with hyperpolarized $^{13}$C MRI, highlighting its potential as a noninvasive biomarker for assessing metabolic alterations and therapeutic response in liver cancer.
  Figure 465-01-014.  Stimulus-Locked Metabolic Response Functions Across ¹H-fMRS, ²H Labeling, and Hyperpolarized ¹³C.
Camille Begon, Fatemeh Anvari Vind, Sotirios Katsikis, Rolf Gruetter, Mor Mishkovsky, Nathalie Just
EPFL, Lausanne, Switzerland
Impact: This work provides a predictive framework for matching stimulation paradigms to MRS modalities, enhancing the sensitivity and interpretability of glutamate imaging. It enables more precise probing of neuroenergetics across timescales, advancing functional MRS as a tool for brain metabolism research.
  Figure 465-01-015.  ¹³C carbonyl polarization via intermolecular water NOE in multiple biomolecules
Elton Montrazi, Korin Butbul, Lucio Frydman
Weizmann Institute, Rehovot, Israel
Impact: We found that ¹³C carbonyls in multiple biomolecules –bicarbonate, acetate, pyruvate, alanine lactate– can be polarized by intermolecular NOE from water. This can be combined with hyperpolarized water, enriching the 13C sensitivity for spectroscopy or imaging purposes.
  Figure 465-01-016.  Understanding metabolic differences in amyloid-beta and tau pathology by in vivo hyperpolarized mri
Julia Zickus, José Enriquez, Khloe Kelley, Bill Sun, Aldo Morales, Jorge DeLaCerda, Xudong Qiu, Muxin Wang, David Piwnica-Worms, Seth Gammon, Jeffrey Wefel, William Ray, Pratip Bhattacharya
The University of Texas MD Anderson Cancer Center, Houston, United States of America
Impact: Current approaches to study AD as a solely plaque-based pathology has been unsuccessful. Diagnostic tools are invasive and expose patients to radioactivity. HP-MRI can distinguish Ab and tauopathies that may delineate the mechanism of AD development and interrogate treatment efficacy.

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