Snapshot whole-brain T1 relaxometry using steady-state prepared spiral multislice variable flip angle imaging

3Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Purpose: Variable flip angle (VFA) imaging is widely used for whole-brain T1 quantification. Because of the requirement to acquire at least two sets of MR images at different flip angles, VFA relaxometry is relatively slow. Here, whole-brain VFA T1 mapping at 1.5 T is accelerated by using efficient spiral non-Cartesian imaging. Methods: To quantify T1 in the human brain, radiofrequency spoiled gradient-echo imaging is performed at two optimized flip angles using an interleaved 2D multislice sequence with high spoiling efficiency. The acquisitions are accelerated by using a spiral trajectory with 10 interleaves combined with a dedicated magnetization preparation to ensure steady-state conditions in minimal time. Results: The investigated MR scan protocol allowed the acquisition of whole-brain T1 maps at a clinically relevant resolution in only 40 s (0.7 s per slice) with high reproducibility. White and gray matter T1 peaks clearly could be delineated by calculation of whole-brain T1 histograms, and the delivered T1 values showed good agreement with the reference method in selected regions of interest. Conclusion: Due to the use of a fast spiral k-space trajectory, whole-brain VFA T1 mapping could be accelerated by an order of magnitude compared to conventional Cartesian sampling. Magn Reson Med 79:856–866, 2018. © 2017 International Society for Magnetic Resonance in Medicine.

Cite

CITATION STYLE

APA

Heule, R., Pfeuffer, J., & Bieri, O. (2018). Snapshot whole-brain T1 relaxometry using steady-state prepared spiral multislice variable flip angle imaging. Magnetic Resonance in Medicine, 79(2), 856–866. https://doi.org/10.1002/mrm.26746

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free