shenghui Xie1, shaoyu Wang2, xu Yan2, huapeng Zhang2, guang Yang3, and yang Gao1
1Department of Radiology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China, 2Siemens Healthineers, Shanghai, China, 3East China Normal University, Shanghai, China
Synopsis
The purpose of this study was to explore the diagnostic value of multimode diffusion imaging in the evaluation of glioma tumor grade and proliferation activity. (DKI) and MAP-MRImodel). The results showed that there were significant differences in MK, RTOP and QIV between high and low grade glioma, and the values of MK and QIV of the tumor parenchyma were positively correlated with ki-67. MK and QIV have great potential in predicting tumor proliferation activity. Multimode diffusion-weighted imaging is valuable for the evaluation of preoperative glioma grade and tumor proliferation activity.
Objective
To
explore the diagnostic value of two types of diffusion models in evaluation of
glioma tumor grade and proliferation activity using advanced diffusion models,
including diffusion kurtosis imaging (DKI) and newly proposed mean apparent
propagator (MAP)-MRI.Materials and methods
42
patients clinically diagnosed as glioma and confirmed by surgery were enrolled
in this prospective study(22 had of low-grade glioma, 20 had of high-grade
glioma). All the patients underwent DKI and MAP-MRI scanning on a 3T MR scanner
(MAGNETOM Skyra, Siemens Healthcare, Erlangen, Germany). DKI parameters were as
follows: TR=5500ms, TE=83.6ms, FOV=220mm×220mm, matrix =110×110, slice
thickness= 4mm, inter-slice spacing = 0, b value = 0, 1000, 2000s/mm2,
30 diffusion directions, scan time = 9min12s. MAP-MRI parameters were as
follows: TR=7000ms, TE=107ms, FOV=220mm×220mm, slice thickness= 3.0mm, matrix
=98×98, the maximum b value = 3000s /mm2. Scan time= 15min40s. DKI data was post-processed
on a Diffusional Kurtosis Estimator(DKE,NITRC) software, DKI parameters
included mean diffusion kurtosis (MK), mean diffusion (MD) and fractional
anisotropy (FA) value. The MAP-MRI parameters were calculated based on an
in-house developed tool with Python, called NeuDiLab, which is based on an
open-resource tool DIPY (Diffusion Imaging In Python, http://nipy.org/dipy).
MAP-MRI parameters included the return-to-the-origin probability (RTOP),
Q-space inverse variance (QIV), mean squared displacement (MSD) and the
non-Gaussianity (NG).The tumor parenchyma was manually delineated and the ROI
of the normal white brain texture on the contralateral side was standardized,
and the differences of each parameter in glioma classification were compared.
The receiver operating characteristic (ROC) curve was used to evaluate the
diagnostic performance of these parameters, and the correlation between each
parameter and ki-67 marker index was analyzed and calculated.Results
There
were statistically significant differences in MK, FA,RTOP、NG and QIV between high and low grade glioma tumor parenchyma
(P<0.05), and QIV and MK had a higher area under ROC curve (0.931 and
0.905). There was no statistically significant difference in MD and MSD between
high and low grade gliomas (P > 0.05). MK and QIV values of tumor parenchyma
were positively correlated with ki-67 (r = 0.682 and 0.694).Discussion
Diffusion
kurtosis imaging (DKI) is an advanced non-gaussian diffusion imaging technique
that provides a more accurate diffusion model to quantify deviations from
gaussian distribution, or kurtosis. By obtaining at least two non-zero
diffusion gradient factors (b values) in more than 15 nonlinear directions, the
kurtosis indexes MK, Ka and Kr as well as the diffusion indexes MD and FA were
obtained.
The
MAP-MRI model does not rely on the prior model. The model uses probability
density function to describe the complete spatial distribution of the diffusion
motion, and accurately distinguishes the local complex interleaving fibers with
excellent angular resolution to obtain a true six-dimensional diffusion image.
Therefore, it is of great significance for heterogeneous classification of
glioma cells.
High-grade
gliomas are characterized by more cells, nuclear atypia, pleomorphism, and
heterogeneity, with angiogenesis, necrosis, hemorrhage, and endothelial cell
proliferation. In contrast, lower-grade gliomas are composed of
well-differentiated cells with lower cell density, larger cells, and more uniform
nests, and also have fewer diffusion barriers.Conclusion
MK and QIV had great potential in predicting
tumor proliferation activity. MK, RTOP, QIV and MK can effectively display the
changes of tumor microstructure. RTOP and QIV not only reflect the diffusion
characteristics of water molecules in the central nervous system, but also
reflect the changes in the microstructure of tissues. Multimode
diffusion-weighted imaging was valuable for the evaluation of preoperative
glioma grade and tumor proliferation activity.Acknowledgements
Thanks to director gao Yang of radiology
department of affiliated hospital of Inner Mongolia medical university for his
guidance on this subject, and thanks to Mr. Wang shaoyu of Siemens scientific
research team and Mr. Yang guang of Shanghai key magnetic resonance laboratory
of east China normal university for their analysis and processing of
experimental data.References
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