Jin Li1, Xiangrong Li1, and Huiting Zhang2
1The First Affiliated Hospital of Guangxi Medical University, Nanning, China, 2MR Scientific Marketing, Siemens Healthineers, Wuhan, China
Synopsis
We explored the applied value of multi-mode MR imaging
technology, including diffusion kurtosis imaging (DKI), arterial spin
labeling (ASL) and 1H-MRS, in glioma tumor invasion
boundary. Results showed mean kurtosis from DKI and apparent diffusion
coefficient had the highest diagnostic efficiency between high-grade (HGG) and low-grade gliomas
(LGG). There were significant differences in CHO/Cr and NAA/Cr from 1H-MRS between
the solid area and the proximal peritumoral edema
area (PEA),
and CHO/Cr and NAA/Cr in different PEA of LGG or HGG. PEA within 1cm around the
solid area is recommended to be resected to decrease recurrence rate.
Purpose
To investigate the applied value of diffusion kurtosis
imaging (DKI), three- dimensional arterial spin labeling (3D-ASL) perfusion
imaging and magnetic resonance spectroscopy (1H-MRS) in the tumor infiltration
boundary of cerebral glioma.Materials and Methods
This
study included 53 pathologically confirmed glioma patients, and all patients underwent
conventional brain magnetic resonance imaging sequences, DKI, 3D-ASL and 1H-MRS
examination before surgery on the MAGTOM Prisma 3T scanner (Siemens Healthcare,
Erlangen, Germany). The scan parameters are as follows: DKI
(repetition time (TR) / echo time (TE)= 2600/92ms, slice thickness = 4mm, field
of view (FOV) = 240×240mm2,
b= 500,1000,1500,2000 and 2500s/mm2, thirty uniformly distributed directtions
for each b-value, and acquisition time = 6min46s), 3D-ASL(TR/ TE =4600/16.18ms,
slice thickness = 3mm, post-label delay (PLD) time = 1990 ms, FOV=192×192mm2,
acquisition time = 4min59s), 1H-MRS(TR/
TE =1700/135ms, slice thickness = 15mm, FOV = 160×160mm2, acquisition
time = 6min53s). In the glioma solid area (GSA) and peritumoral edema area (PEA) around the solid area (<1cm,
proximal; 1~2cm, moderate; >2cm, distal), the parameters, including apparent
diffusion coefficient (ADC), mean, axis and radial kurtosis (MK, AK, RK) from
DKI, relative cerebral blood flow (rCBF) from ASL, and CHO/Cr and NAA/Cr from
MRS, were compared between high-grade (HGG) and low-grade gliomas (LGG) using
t-test or Kruskal-Wallis test. P < 0.05 was considered statistically
significant. Then, the receiver operating characteristic (ROC) curve was
plotted for the significantly different indexes to calculate their sensitivity,
specificity, area under the curve (AUC) and diagnostic threshold.Results
Among
the enrolled 53 patients (24 females, mean age 40±15), 31 had LGG and 22 had HGG. The
MK, AK, RK, rCBF and CHO/ Cr values of GSA in the HGG were higher than those in
the LGG, and the ADC values of GSA in the HGG were lower than that in the LGG (P
< 0.05). The MK value (AUC, 0.873; 95% CI, 0.781-0.965; P<0.01;
sensitivity, 81.8%; specificity, 83.9%) had the highest diagnostic efficacy for
HGG, with a threshold of 0.728. In addition, the ADC value (AUC, 0.811; 95%CI,
0.698-0.924; P<0.01; sensitivity, 58.1%; specificity, 95.5%) had a certain
diagnostic value for LGG, with the threshold of 0.892×10-3 mm2/s. The results
are shown in Table 1,2
and Figure 1.
In the
HGG, there were statistically significant differences in MK, AK, RK, ADC, rCBF, CHO/Cr and NAA/Cr values
between the solid area and the proximal PEA, in CHO/Cr between the proximal and
moderate PEA, and in NAA/Cr between moderate and distal PEA (P<0.05). In the
LGG, there were statistically significant differences in NAA/Cr and CHO/Cr
between the glioma solid area and the proximal PEA, and in NAA/Cr between the
proximal and distal PEA (P<0.05). There was no statistical difference in
every index of PEA between HGG and LGG (P>0.05). The results are shown in Table 3.
Discussion and Conclusion
Our
study showed that DKI,
3D-ASL and 1H-MRS
can identify high-grade glioma and low-grade glioma by the parameters of the glioma
solid area, and the MK and ADC values have the highest diagnostic efficacy in
predicting the glioma grade. MK > 0.728 reveals a high probability of high-grade
glioma, while ADC > 0.892×10-3
mm2/s suggests a great probability of low-grade glioma. MK represents
the complexity of the tissue elements, so the higher MK in the high-grade
glioma suggests the more complex elements, which is
consistence with
the previous study[1-5]. However, unlike this study, ADC values have not been used as a parameter
index for research. In
addition, through the comparison of the solid area and the different regions of
peritumoral edema area, we found that the CHO/Cr value can differentiate the
solid area and the proximal peritumoral edema area in both the high-grade and
low-grade glioma. Moreover, it has a significant difference between the proximal
and moderate peritumoral edema area in the high-grade glioma. These findings mean that there was tumor cell infiltration
in the proximal peritumoral edema area. This
is similar to the conclusion
of Blystad I et al [6]. They found that there was a significant statistical
difference between peritumoral edema area and normal appearing white matter by
using quantitative R1‑difference‑maps. In contrast, our study
divided PEA into three regions in detail, proximal, moderate and distal. We
also found that CHO/Cr
values can be regarded as a noninvasive and effective supplementary method to
evaluate the invasive boundary of the glioma. Association studies of this are still rare. It is suggested that the range of
surgical resection is to maximize the removal of the GSA and the PEA within 1cm
under the premise of ensuring the functional area of the brain.
Acknowledgements
We sincerely thank all those who have contributed to this research project.References
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