English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Rapid whole-brain quantitative MT imaging

MPS-Authors
/persons/resource/persons216029

Heule,  R       
Institutional Guests, Max Planck Institute for Biological Cybernetics, Max Planck Society;

Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Afshari, R., Santini, F., Heule, R., Meyer, C., Pfeuffer, J., & Bieri, O. (2023). Rapid whole-brain quantitative MT imaging. Zeitschrift für Medizinische Physik, Epub ahead. doi:10.1016/j.zemedi.2023.02.005.


Cite as: https://hdl.handle.net/21.11116/0000-000C-EC67-7
Abstract
Purpose: To provide a robust whole-brain quantitative magnetization transfer (MT) imaging method that is not limited by long acquisition times.
Methods: Two variants of a spiral 2D interleaved multi-slice spoiled gradient echo (SPGR) sequence are used for rapid quantitative MT imaging of the brain at 3 T. A dual flip angle, steady-state prepared, double-contrast method is used for combined B1 and-T1 mapping in combination with a single-contrast MT-prepared acquisition over a range of different saturation flip angles (50 deg to 850 deg) and offset frequencies (1 kHz and 10 kHz). Five sets (containing minimum 6 to maximum 18 scans) with different MT-weightings were acquired. In addition, main magnetic field inhomogeneities (ΔB0) were measured from two Cartesian low-resolution 2D SPGR scans with different echo times. Quantitative MT model parameters were derived from all sets using a two-pool continuous-wave model analysis, yielding the pool-size ratio, F, their exchange rate, kf, and their transverse relaxation time, T2r.
Results: Whole-brain quantitative MT imaging was feasible for all sets with total acquisition times ranging from 7:15 min down to 3:15 min. For accurate modeling, B1-correction was essential for all investigated sets, whereas ΔB0-correction showed limited bias for the observed maximum off-resonances at 3 T.
Conclusion: The combination of rapid B1-T1 mapping and MT-weighted imaging using a 2D multi-slice spiral SPGR research sequence offers excellent prospects for rapid whole-brain quantitative MT imaging in the clinical setting.