Min-xiong Zhou1, Huiting Zhang2, Yang Song3, Guang Yang3, and Xu Yan2
1Shanghai University of Medicine & Health Sciences, Shanghai, China, 2MR Scientific Marketing, Siemens Healthcare, Shanghai, China, 3Shanghai Key Laboratory of Magnetic Resonance, East China Normal Univeristy, Shanghai, China
Synopsis
Advanced diffusion models such as NODDI, MAP-MRI are of high interests
in brain research, but suffer from long acquisition time. Advanced
under-sampling scheme were reported in previous studies for acceleration but
are not commercially available. This study evaluates a simple and commercial
available under-sampling scheme using the symmetric property of q-space, which
could accelerate the acquisition by 2 fold. Results showed that it did not
significant sacrifice the accuracy of quantitative maps. In addition, a
symmetrically data copy step is needed to improve the estimation accuracy for both
MAP-MRI and NODDI models.
Introduction
Diffusion-weighted
MRI (DWI) is a powerful technique to probe the tissue microstructural changes and
provide a range of quantitative scalar metrics across the whole brain. Diffusion
tensor imaging (DTI) has been widely used to previous studies. Recently
advanced diffusion models were proposed, such as Neurite orientation dispersion
and density imaging (NODDI) and Mean apparent propagator (MAP)-MRI, which can reflect
complicated tissue characteristics, such as the degree of fanning of fibers, the
axonal density, the diffusion anisotropy and the non-Gaussian character of the
three-dimensional diffusion process1. However, normally a large dataset
is needed for these models with multiple b-value and diffusion gradient
directions, result in long scan time hardly acceptable in clinical application.
Previous studies reported that multiband2 and advanced under-sampling
schemes3,4 could significantly reduce the scanning time, while the
under-sampling schemes could bias the parameters. Besides this drawback, the
advanced under-sampling schemes are not available in commercial MR scanner,
thus making it difficult for widely application in clinical routine. In this
study, we evaluate a simple half-under-sampling scheme (2 fold acceleration) using
the symmetrical property of gradient direction distribution in conventional diffusion
spectrum imaging (DSI) technique, which is becoming commercially available recently.
Its influence for quantitative parameters of NODDI, MAP-MRI models was investigated.Methods
Two
patients with brain tumor were enrolled and underwent MRI scanning using a 3T MR
scanner (MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany). The DSI data
were acquired using a fully Cartesian q-space grid scheme. The DSI parameters
were as follows: TR/TE = 3900/72 ms, FOV = 220 × 220 mm2, matrix =
128 × 128, slice thickness = 2 mm, in-plane acceleration factor = 2, slice
acceleration factor = 2, diffusion time δ/Δ = 15.9/35.0 ms, bmax =
3000 s/mm2, two b=0 data and 98 DWI data with a radius of three
samples, total scan time = 6 min 42 s. A symmetric q-space scheme is used here.
Three
q-space sampling schemes were compared in the study: 1) Full sampled data with
all 98 directions, denotes as Full;
2) a half-sphere under-sampled data with 49 non-parallel directions, denotes as
Half; 3) a half-sphere under-sampled
data with 49 non-parallel direction, and the other half data are symmetrically copied
from the acquired data, denotes as Half-to-Full.
Eddy currents distortion and subject motion was corrected using bneddy tool of DiffusionKit
software5. The NODDI and MAP-MRI parameters from the three sampling schemes
were calculated using an in-house developed software called NeuDiLab, which is
based on an open-resource tool DIPY (Diffusion Imaging In Python, http://nipy.org/dipy).
The NODDDI parameters included intracellular volume fraction (ICVF) and
orientation dispersion index (ODI). The MAP-MRI parameters included the return
to the origin probability (RTOP) and Non-Gaussianity (NG). The percent of square
coefficient of variation (CV) was used to assess the differences for three
reconstruction schemes.Results
Figure 1 shows parameter maps from the NODDI model and their
corresponding CV for one patient using three sampling schemes, and Figure 2
shows the results from MAP-MRI model. Refer to Full scheme, the Half-to-Full
scheme showed smaller CV than the Half scheme for all parameters of MAP-MRI
model. While for NODDI model, similar CV was found for Half and Half-to-Full
scheme, and Half-to-Full scheme showed slightly smaller CV than Half scheme in
ICVF maps, especially in the around regions of tumor. Figure 3 shows scatter
plots of quantitative parameters from Full scheme against Half or Half-to-Full
scheme on voxel-by-voxel basis for the whole brain. The parameter NG showed a
obvious bias for Half scheme, while Half-to-Full scheme showed no bias against
the Full scheme. Discussion
In this study, the quantitative parameters of NODDI and MAP-MRI models were
compared among three diffusion sampling schemes. The results found that Half-to-full
scheme outperformed the Half scheme with smaller difference of quantitative parameters
referred to the Full scheme, especially for the MAP-MRI parameters. It means
that the MAP-MRI model estimation were more sensitive to the DWI sampling
schemes than NODDI metrics, which =is consistent with the findings of previous
studies3,4. In addition, the symmetric data copying step can
effectively reduce estimation error.
To
conclude, this study showed that the acquisition time of advanced diffusion
models could be efficiently reduced by using half q-space sampling scheme in
combination with symmetrically data copying to fill the other half data. Thus,
this acceleration scheme could be applied widely in clinical routine or for
special patient group such as children.Acknowledgements
No acknowledgement found.References
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