Publication

Pulseq-CEST: Towards multi-site multi-vendor compatibility and reproducibility of CEST experiments using an open-source sequence standard

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Last modified
  • 09/05/2025
Type of Material
Authors
    Kai Herz, Max Planck Institute for Biological CyberneticsSebastian Mueller, Max Planck Institute for Biological CyberneticsOr Perlman, Massachusetts General HospitalMaxim Zaitsev, Medical University of ViennaPhillip Zhe Sun, Emory UniversityLinda Knutsson, Lund UniversityJinyuan Zhou, Johns Hopkins UniversityPeter van Zijl, Johns Hopkins UniversityKerstin Heinecke, Phys Tech BundesanstaltPatrick Schuenke, Phys Tech BundesanstaltChristian T Farrar, Massachusetts General HospitalManuel Schmidt, Friedrich Alexander Univ Erlangen NurnbergArnd Dörfler, Friedrich Alexander Univ Erlangen NurnbergKlaus Scheffler, Max Planck Institute for Biological CyberneticsMoritz Zaiss, Max Planck Institute for Biological Cybernetics
Language
  • English
Date
  • 2021-10-01
Publisher
  • WILEY
Publication Version
Copyright Statement
  • © 2021 International Society for Magnetic Resonance in Medicine
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 86
Issue
  • 4
Start Page
  • 1845
End Page
  • 1858
Supplemental Material (URL)
Abstract
  • Purpose: As the field of CEST grows, various novel preparation periods using different parameters are being introduced. At the same time, large, multisite clinical studies require clearly defined protocols, especially across different vendors. Here, we propose a CEST definition standard using the open Pulseq format for a shareable, simple, and exact definition of CEST protocols. Methods: We present the benefits of such a standard in three ways: (1) an open database on GitHub, where fully defined, human-readable CEST protocols can be shared; (2) an open-source Bloch-McConnell simulation to test and optimize CEST preparation periods in silico; and (3) a hybrid MR sequence that plays out the CEST preparation period and can be combined with any existing readout module. Results: The exact definition of the CEST preparation period, in combination with the flexible simulation, leads to a good match between simulations and measurements. The standard allowed finding consensus on three amide proton transfer–weighted protocols that could be compared in healthy subjects and a tumor patient. In addition, we could show coherent multisite results for a sophisticated CEST method, highlighting the benefits regarding protocol sharing and reproducibility. Conclusion: With Pulseq-CEST, we provide a straightforward approach to standardize, share, simulate, and measure different CEST preparation schemes, which are inherently completely defined.
Author Notes
  • Kai Herz, Max Planck Institute for Biological Cybernetics, Max-Planck-Ring 11, 72076 Tuebingen, Germany. Email: kai.herz@tuebingen.mpg.de
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