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

Digital Poster

Spectroscopy and Spectroscopic Imaging: Methods

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Spectroscopy and Spectroscopic Imaging: Methods
Digital Poster
Contrast Mechanisms
Wednesday, 13 May 2026
Digital Posters Row J
16:00 - 16:55
Session Number: 569-05
No CME/CE Credit
This session highlights recent methodological advances in MR spectroscopy and spectroscopic imaging.
Skill Level: Advanced

  Figure 569-05-001.  Simultaneous detection of GABA and Glycine using MEGA-PRESS with TE optimization at 3T
Justin Singer, Kimberly Chan
University of Texas Southwestern Medical Center, Dallas, United States of America
Impact: The simultaneous measurement of GABA and glycine by 1H-MRS grants a more comprehensive profile of inhibitory tone without the expense of additional scans or reduction in GABA+ data quality.
  Figure 569-05-002.  Multi-center Validation of Plug'n Play 3D MRSI at 7 T Using an Online Reconstruction: A Song of ICE and FIRE
Bernhard Strasser, Korbinian Eckstein, Lukas Hingerl, Aaron Osburg, Hauke Fischer, Paul Weiser, Ekaterina Sazonova, Antoine Klauser, Ovidiu Andronesi, Yan Li, Jing Liu, Amirmohammad Shamaei, Barbara Dymerska, Martina Callaghan, Zeinab Eftekhari, Thomas Shaw, Markus Barth, Stanislav Motyka, Gilbert Hangel, Wolfgang Bogner
High-field MR Center, Vienna, Austria
Impact: This work enables fast, automated, and standardized 3D MRSI online reconstruction and fitting directly on the scanner, drastically reducing processing time and data size while improving reproducibility across sites—paving the way for multi-center studies in MRSI.
  Figure 569-05-003.  Comparing whole slice and localized brain rosette spectroscopic imaging at 3T
Emile Kadalie, Chathura Kumaragamage, Michel Lauzon, Mervyn Singh, Milton Camacho, Filomeno Cortese, Vicente Enguix, Neta Bar Am, Sneha Senthil, Ashley Harris , Gregory Lodygensky, Jamie Near
Sunnybrook Research Institute, Toronto, Canada
Impact: This work demonstrates that whole-slice rosette MRSI with post-processing lipid removal can achieve spectral quality comparable to PRESS-localized acquisitions, enabling improved brain coverage without rectangular localization, and without compromising metabolite quantification.
  Figure 569-05-004.  Whole-Brain Functional MRSI Using ECCENTRIC at 7T: Proof-of-Concept and Feasibility
Francesca Saviola, Antoine Klauser, Dimitri Van De Ville
École polytechnique fédérale de Lausanne - EPFL, Lausanne, Switzerland
Impact: This study leverages a recently proposed 7T functional MRSI to enable unprecedented whole-brain neurochemical mapping during cognitive and perceptual tasks. This protocol overcomes spatial limitations of traditional single-voxel fMRS, potentially enhancing understanding of metabolic dynamics in health and disease.
  Figure 569-05-005.  Quantitative 1H MRS in gray and white matter in the human brain with localized B1+ shimming at 11.7T
Alfredo Lopez Kolkovsky, Franck Mauconduit, Vincent Gras, Aurélien Massire, Son Chu, Shajan Gunamony, Nicolas Boulant, Alexis Amadon, Fawzi Boumezbeur
CEA NeuroSpin, Paris-Saclay University, CNRS, Gif-Sur-Yvette, France
Impact: This study opens the way for quantitative single-voxel 1H MRS in the human brain at 11.7T. The increased sensitivity and spectral resolution allow for short acquisition scans with elevated quantification accuracy.
  Figure 569-05-006.  TriPeak optimal combination: A multichannel X-nuclear MRSI coil combination method providing optimal SNR and zero bias
Jiying Dai, Dennis Klomp, Alexander Raaijmakers
University Medical Center Utrecht, Utrecht, Netherlands
Impact: The proposed TriPeak coil combination method enables bias-free, optimal-SNR reconstruction for X-nuclear MRSI, overcoming the limitations of traditional combinations. Its validated in silico and in vivo performance enhances spectral accuracy, improves quantitative reliability and advances metabolic imaging in low-sensitivity nuclei.
  Figure 569-05-007.  Robust Coil Combination for Low-SNR X-Nuclear MRSI
Rolf Schulte, Yang Fan, Chunsheng Wang, Feng Chen, Frank Riemer, Pierfrancesco Ambrosi, Paolo Cecchi, Michela Tosetti, Alixander Khan, Esben Hansen, Michael Væggemose, Christoffer Laustsen
GE Healthcare, Munich, Germany
Impact: In order to move X-nuclear MR into clinical routine, robust methods dealing with limited SNR are required. Multi-channel receive coils can improve spatial coverage and SNR, but require robust and fully-automatic coil combination methods for reproducible, high-SNR results.
  Figure 569-05-008.  Absolute MR Thermometry for RF Safety Assessment Using Spectroscopy and Metabolite Cycling
Mathijs Kikken, Koen Custers, Ettore Flavio Meliado, Cornelis van den Berg, Alexander Raaijmakers
University Medical Center Utrecht, Utrecht, Netherlands
Impact: A noninvasive MR spectroscopy–based approach is demonstrated for local absolute tissue temperature measurements, which could provide a more comprehensive understanding of RF-induced heating and serve as a biomarker for physiological and pathological conditions.
  Figure 569-05-009.  SpectroA: A Multi-Sequence MRS Package for Comprehensive MR-Detectable Neurochemical Profiling
Manoj Kumar Sarma, Saipavitra Murali-Manohar, Ioannis-Angelos Giapitzakis, Johanna Dorst, Bei Zhang, Anke Henning
University of Texas Southwestern Medical Center, Dallas, United States of America
Impact: The AIRC MRS sequence package enables high-quality, reproducible single-voxel 1H and 31P spectroscopy with robust B0 shimming, and optimized sequences, enhancing metabolic characterization, biomarker identification, personalized treatment, and translational research across clinical and research applications.
  Figure 569-05-010.  Time-Domain Quantitative Decomposition of MRS FID Signals: Comparison of Hankel SVD and Pade Transform Methods
Jian-xiong Wang
The University of Alabama at Birmingham, Birmingham, United States of America
Impact: Direct time-domain decomposition using Hankel SVD and Fast Padé Transform enables accurate quantification of weak metabolite peaks in hyperpolarized [2-¹³C]pyruvate MRS without phase correction, providing a major advance in quantitative metabolic spectroscopy with large dynamic range signals.
  Figure 569-05-011.  Simultaneous mapping metabolite and water T1, T2, absolute concentration using fast MR spectroscopic fingerprinting imaging
Shiyang You, Yi-Cheng Hsu, Yingchao Liu, Peng Zhao, Chenting Ye, Min Wang
College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, China
Impact: MRSFI based on Csar-EPSI enables ultrafast simultaneous mapping of metabolite and water T₁, T₂ and absolute concentration, providing a new framework for multiparametric spectroscopic imaging with potential applications in detecting pathological metabolic alterations and functional dynamics in the brain.
  Figure 569-05-012.  Can AI Assess MRS Data Quality from Single Transients?
Shuyuan Wang, Aaron Gudmundson, Christopher Davies-Jenkins, Yulu Song, Georg Oeltzschner, Richard AE Edden
Johns Hopkins University School of Medicine, Baltimore, United States of America
Impact: The network presented here demonstrates the potential for developing automated feedback, adaptive acquisition strategies, and more advanced AI (i.e., agents) in clinical settings. The proposed architecture is lightweight and opens possibilities for real-time monitoring.
  Figure 569-05-013.  Generalization analysis of low-rank regularized fine-tuning-based deep learning for magnetic resonance spectroscopy denoising
Jian Cao, Tianyu Qiu, Di Guo, Zhangren Tu, Yihui Huang, Chunyan Xiong, xianwang jiang, Xiaobo Qu
Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance, Xiamen University, Xiamen, China
Impact: Leverage implicit regularization of DNNs for pre-training and theoretically grounded explicit regularization to enhance low-rank structure and generalization in fine-tuned models, reaching high-quality MRS denoising.
  Figure 569-05-014.  A novel MRS fingerprinting approach to estimate concentrations and relaxation times of metabolites, macromolecules, and water
Helge Zöllner, Zahra Shams, Julia Stabinska, Kimberly Chan, Assaf Tal, Georg Oeltzschner, Richard AE Edden, Peter Barker
Johns Hopkins University School of Medicine, Baltimore, United States of America
Impact: A 10-minute MRSF experiment allows for fast and subject-specific estimation of metabolite, macromolecule, and water concentrations and relaxation times. This comprehensive biochemical profile is particularly interesting for applications in neurological diseases characterized by concurrent microenvironmental and metabolic changes.
  Figure 569-05-015.  Deep Learning–based Denoising of Magnetic Resonance Spectroscopy using a Denoising Autoencoder
Kou Kumagai, Hitoshi Kubo, Koshi Shigiyama, Urara Hirano, Takashi Iwanaga
Fukushima Medical University, Fukushima, Japan
Impact: DAE-based denoising enables reliable metabolite quantification from short-acquisition MRS, providing a foundation for dynamic metabolic imaging with clinically feasible temporal resolution.
  Figure 569-05-016.  Suppression of macromolecule signal removes the association between GABA+ and age
Tiffany Bell, Priya Chander, Ashley Harris
University of Reading, Reading, United Kingdom
Impact: Associations observed with GABA+ do not replicate when using macromolecule suppressed (MM-Sup) GABA measures, indicating macromolecules may drive these associations. Research using GABA+ measures needs to be mindful of macromolecule contamination when interpreting the data and temper conclusions accordingly.

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