Problem: The clinical utility of myelin water fraction (MWF) mapping based on multi-echo-spin-echo (MESE) T2-relaxometry is prohibitively slow (~90-120 minutes for acquisition matrix 128x128x50; TR 3s). MWF-values from T2-prep based approach and mcDESPOT (Multicomponent-driven-equilibrium-single-pulse-observation-of-T1-and-T2) matches poorly with MESE based quantification.
Methods: We compare GRASE (Gradient-and-Spin-Echo) based MWF quantifications against those from MESE and compare our algorithm against current state of the art. 3D non-selective GRASE, MESE were optimized. Implemented post-processing method utilizes spatial correlations in 3D local neighborhoods to improve noise stability, while simultaneously accounting for stimulated echo contributions.
Results & Conclusions: Results demonstrate good consistency between both sequences.
The clinical utility of myelin water fraction (MWF) mapping based multi-echo-spin-echo (MESE) T2-relaxometry is impeded due to prohibitively slow scan time, needing ~60-90 minutes for whole brain coverage (matrix 128x128x50; TR 3 sec). There are alternative clinical feasible methods to measure MWF-maps, such as T2-prep based approach and mcDESPOT (Multicomponent-driven-equilibrium-single-pulse-observation-of-T1-and-T2), though they do not show good correspondence with MESE based MWF-quantification1-5. The purpose of this study is to evaluate the effect of filling up outer k-space using gradient echoes on MWF-quantification in GRASE (gradient and spin echo) based quantifications. ROI-averaged MWF-values extracted using 3D non-selective GRASE have been shown to correspond very well with corresponding values from 3D non-selective MESE6; those voxelwise match appear less consistent.
We have recently proposed an expectation-maximization (EM) based algorithm (submitted in another abstract; also refer to Fig 1 for flow chart), which utilizes the local spatial correlation in 3 dimensional neighborhood to improve noise stability of underlying T2-distributions. In this abstract, we compare the performance of our EM based algorithm against that proposed by Prasloski et al.7. We demonstrate better consistency with MESE-based quantification in WM-tracts.
For a known flip angle error (FAE), the T2-decay can be written as the linear function of underlying T2 distributions (x)8: yEPG = AEPGx + ε, with AEPG(i,j) = intensity at echo time-point TE(i) due to unit water fraction at T2 value T2(j) . The single voxel parameters x, y, ε can be stacked as multi voxel column vectors $$$\overline{x}, \overline{y}, \overline{\epsilon}$$$ and the corresponding multi voxel equivalent can be written as: $$$\overline{y} = A_{MV}\overline{x}+\overline{\epsilon}$$$ . Here, AMV is the block diagonal matrix, constructed with voxelwise-AEPG along its block. It was previously shown8 that by simultaneous implementation of conventional and spatial regularization, a more noise robust reconstruction of MWF-map is possible:
$$\widehat{x} = arg min_x {||A_{MV}\overline{x}- \overline{y} ||}^2+M_T{||\overline{x}||}^2+\mu_s{||D_s \overline{x}||}^2$$
Data: QT2R data was acquired from 2 healthy volunteers using CPMG based non-selective MESE and GRASE sequences (3T Philips-Ingenia) with: axial FOV 230x190 mm, voxel resolution 2 x 2 x 3.5 mm3, receiver bandwidth 355 kHz, 12 slices, TR 2000 ms, 32 echoes, SENSE-factor: inplane = 2 & Slice-encoding = 2; echo spacing 6 ms; Average 2. Additionally, EPI-factor of 3 was used for GRASE sequence. It took ~14 and ~42 minutes to acquire MESE and GRASE data with limited coverage. Average of 2 was essential for the FID correction.
Algorithm: The flow-chart is shown in Fig 1. As an initialization step, first the joint estimation of μT-map and flip angle error map (or equivalently B1-error) is performed using extended L-curve approach. Following this, we iteratively improve over T2-distribution map (M-step) and refine over flip angle error until the convergence of solutions (T2 distributions). In practice, the convergence is achieved with in fourth iteration.
This project was partly supported by the National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health (Grant Number P41-EB015893) and the National Institute of Neurological Disorders and Stroke (Award Number R01NS087516).
All authors would like to thank Dr. Hendrik Kooijman, Philips Healthcare, Hamburg, Germany for providing valuable support and guidance regarding the optimization of sequence. We would also like to thank Prof. Stephen Becker, Applied Mathematics, University of Colorado at Boulder, USA for sharing his L-BFGS-B code. We would also like to thank Mr. Mohamad Nawab Alam, Dept. of Electric Engineering, Indian Institute of Technology, Roorkee, India for help in develop genetic algorithm for minimizing expression in E-step, though it was not used in here as we were able to get better performance from “lsqnonlin” solver.
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