Cerebrospinal fluid-suppressed T -weighted MR imaging at 7 T for human brain.

Magn Reson Med

Magnetic Resonance Research Center, Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.

Published: May 2019

Purpose: T -weighted lesional imaging is most commonly performed using inversion recovery turbo spin echoes. At 7 T, however, this acquisition is limited for specific absorption rate and resolution. This work describes and implements a method to generate CSF-suppressed T -weighted imaging.

Methods: The strategy uses a driven equilibrium spin-echo preparation within an inversion recovery with multiple 3D gradient-echo imaging blocks. Images are combined using the self-normalization approach, which achieves CSF suppression through optimized timing of individual blocks and minimizes sources of variation due to coil receptivity, T , and proton density. Simulations of the magnetization-prepared fluid-attenuated inversion recovery gradient-echo (MPFLAGRE) method over T and T relaxation values are performed, and in vivo demonstrations using an 8 2 transceiver array in healthy controls are shown.

Results: The specific absorption rate of the calculated MPFLAGRE sequence is 11.1 ± 0.5 W (n = 5 volunteers), which is 74 ± 2% of the US Food and Drug Administration guidelines. This method acquires both contrasts for CSF suppression with detection of long T components and T -weighted imaging in a single acquisition. In healthy controls, the former contrast generates increased signal in the cortical rim and ependyma. A comparison is shown with a conventional 3D SPACE fluid-attenuated inversion recovery acquisition, and sensitivity to pathology is demonstrated in an epilepsy patient.

Conclusion: As applied with the 8 2 transceiver, the MPFLAGRE sequence generates both whole-brain contrast suitable for lesional and T -weighted imaging at 7 T in fewer than 10 minutes within the US Food and Drug Administration's specific absorption rate guidelines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590483PMC
http://dx.doi.org/10.1002/mrm.27598DOI Listing

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