Arjama Halder1, Chad T. Harris2, Curtis N. Wiens2, Andrea Soddu3, and Blaine A. Chronik3
1Medical Biophysics, Western University, London, ON, Canada, 2Synaptive Medical, Toronto, ON, Canada, 3Western University, London, ON, Canada
Synopsis
Keywords: Low-Field MRI, Low-Field MRI, T2*,subcortical brain,SNR
Motivation: Accurate knowledge of T2* relaxation times is important for optimizing contrast and SNR in multi-echo gradient echo sequences.
Goal(s): To measure the nominal T2* relaxation parameter at 0.5 T over subregions in the brain.
Approach: A 2 mm isotropic 3D multi-echo GRE sequence was acquired in 5 healthy volunteers. T2* estimates were computed over regions of interest using a mono-exponential fit.
Results: T2* estimates of gray (86±8 ms) and white (78±5 ms) matter are in good agreement with previously published measurements in the mid-field. In the deep brain, average T2* values ranged between 70±2 ms to 89±5 ms.
Impact: For optimal T2* contrast in the brain at 0.5 T, echoes from multi-echo acquisitions should extend beyond 60 ms. For optimal SNR, echoes should be combined with a target T2* of ~80 ms.
INTRODUCTION
The recent renaissance in mid-field imaging with high-performance system components merits re-optimization of many pulse sequences. Accurate knowledge of T2* relaxation times in brain tissue is important for optimizing contrast in gradient echo sequences. In particular, for creating phase SNR optimal echo combination weighting coefficients for susceptibility weighted imaging (SWI) [1]. However, reported values of T2* in tissue at 0.5 T are sparse. In this work, we characterize the T2* relaxation parameter of common subgroups of the normal human brain at 0.5 T.METHOD
All imaging protocols were performed on a head-only 0.5 T MR scanner equipped with a high-performance gradient system and 16-channel head coil (Synaptive Medical, Toronto, ON, Canada). Imaging was performed on five healthy volunteers (male, age = 38 ± 8) with informed consent in compliance with health and safety protocols.
Segmentation of 3D T1-Weighted Imaging
Structural images were acquired at 1.1 mm isotropic resolution using a T1-weighted MPRAGE sequence with field of view (FOV) = 236 mm × 236 mm × 180 mm, zipped to a matrix size = 512 × 512 × 320, flip angle (FA) = 9◦, TE = 5 ms, and TR = 11.2 ms. Region of interest (ROI) masks were created for various brain regions using FMRIB’s Automated Segmentation Tool (FAST) and Integrated Registration and Segmentation Tool (FIRST) [2,3].
T2* Mapping of Segmented Regions
A 2 mm isotropic resolution 3D multi-echo GRE (meGRE) sequence was used with FOV = 240 mm × 240 mm × 120 mm, matrix size = 120 × 120 × 60, FA = 32◦ , TE (1) = 5 ms, echo spacing = 3.4 ms, echo train length (ETL) = 26, and TR = 97.25 ms. The 3D meGRE images were registered to the structural image using FMRIB’s Linear Image Registration Tool (FLIRT) [4,5]. Voxel-wise estimates of T2* were computed over the ROIs by fitting the data to a mono-exponential decay model [6].RESULTS
An exemplary structural image showing locations of the ROI masks is shown in figure 1. Figure 2 displays the respective T2* map for this volunteer over the masked ROIs. Individual and aggregate T2* values over notable brain regions are reported in Table 1.DISCUSSION AND CONCLUSION
The T2* relaxation parameter was measured at 2 mm isotropic resolution in the brain of five healthy volunteers at 0.5T. The measurements of gray (86 ± 8 ms) and white (78 ± 5 ms) matter are in good agreement with recent measurements for gray (86 ± 9 ms) and white (72 ± 12 ms) matter performed at 0.55 T [7]. To our knowledge, estimates of T2* in the subcortical brain at 0.5T have not been reported elsewhere in the literature.
In the deep brain, average T2* values across subjects ranged between 70 ± 2 ms and 89 ± 5 ms. Therefore, for optimal T2* contrast, echoes from multi-echo acquisitions should extend beyond 60 ms; and for optimal SNR, they should be combined with a target T2* value of ~80 ms.Acknowledgements
No acknowledgement found.References
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