Article 2019

Relaxation-compensated APT and rNOE CEST-MRI of human brain tumors at 3 T

{Purpose: Relaxation-compensated CEST-MRI (i.e., the inverse metrics magnetization transfer ratio and apparent exchange-dependent relaxation) has already been shown to provide valuable information for brain tumor diagnosis at ultrahigh magnetic field strengths. This study aims at translating the established acquisition protocol at 7 T to a clinically relevant magnetic field strength of 3 T. Methods: Protein model solutions were analyzed at multiple magnetic field strengths to assess the spectral widths of the amide proton transfer and relayed nuclear Overhauser effect (rNOE) signals at 3 T. This prior knowledge of the spectral range of CEST signals enabled a reliable and stable Lorentzian-fitting also at 3 T where distinct peaks are no longer resolved in the Z-spectrum. In comparison to the established acquisition protocol at 7 T, also the image readout was extended to three dimensions. Results: The observed spectral range of CEST signals at 3 T was approximately $\pm$15 ppm. Final relaxation-compensated amide proton transfer and relayed nuclear Overhauser effect contrasts were in line with previous results at 7 T. Examination of a patient with glioblastoma demonstrated the applicability of this acquisition protocol in a clinical setting. Conclusion: The presented acquisition protocol allows relaxation-compensated CEST-MRI at 3 T with a 3D coverage of the human brain. Translation to a clinically relevant magnetic field strength of 3 T opens the door to trials with a large number of participants, thus enabling a comprehensive assessment of the clinical relevance of relaxation compensation in CEST-MRI.}

Author(s): Goerke, S and Soehngen, Y and Deshmane, A and Zaiss, M and Breitling, A and Boyd, PS and Herz, K and Zimmermann, F and Klika, KD and Schlemmer, H-P and Paech, D and Ladd, ME and Bachert, P
Journal: {Magnetic Resonance in Medicine}
Volume: 82
Number (issue): 2
Pages: 622--632
Year: 2019
Publisher: Wiley-Liss
Bibtex Type: Article (article)
DOI: 10.1002/mrm.27751
Address: New York
Electronic Archiving: grant_archive

BibTex

@article{item_3047040,
  title = {{Relaxation-compensated APT and rNOE CEST-MRI of human brain tumors at 3 T}},
  journal = {{Magnetic Resonance in Medicine}},
  abstract = {{Purpose: Relaxation-compensated CEST-MRI (i.e., the inverse metrics magnetization transfer ratio and apparent exchange-dependent relaxation) has already been shown to provide valuable information for brain tumor diagnosis at ultrahigh magnetic field strengths. This study aims at translating the established acquisition protocol at 7 T to a clinically relevant magnetic field strength of 3 T. Methods: Protein model solutions were analyzed at multiple magnetic field strengths to assess the spectral widths of the amide proton transfer and relayed nuclear Overhauser effect (rNOE) signals at 3 T. This prior knowledge of the spectral range of CEST signals enabled a reliable and stable Lorentzian-fitting also at 3 T where distinct peaks are no longer resolved in the Z-spectrum. In comparison to the established acquisition protocol at 7 T, also the image readout was extended to three dimensions. Results: The observed spectral range of CEST signals at 3 T was approximately $\pm$15 ppm. Final relaxation-compensated amide proton transfer and relayed nuclear Overhauser effect contrasts were in line with previous results at 7 T. Examination of a patient with glioblastoma demonstrated the applicability of this acquisition protocol in a clinical setting. Conclusion: The presented acquisition protocol allows relaxation-compensated CEST-MRI at 3 T with a 3D coverage of the human brain. Translation to a clinically relevant magnetic field strength of 3 T opens the door to trials with a large number of participants, thus enabling a comprehensive assessment of the clinical relevance of relaxation compensation in CEST-MRI.}},
  volume = {82},
  number = {2},
  pages = {622--632},
  publisher = {Wiley-Liss},
  address = {New York},
  year = {2019},
  slug = {item_3047040},
  author = {Goerke, S and Soehngen, Y and Deshmane, A and Zaiss, M and Breitling, A and Boyd, PS and Herz, K and Zimmermann, F and Klika, KD and Schlemmer, H-P and Paech, D and Ladd, ME and Bachert, P}
}