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Annals of Clinical and Medical
Case Reports
ReviewArticle ISSN 2639-8109 Volume 9
Shesnia Salim*
and Padikkalakandy Cheriyath
First Hospital of Dalian medical University, China
Texture Analysis of Quantitative ADC Maps to Differentiate Low from High Grade
Glioma
*
Corresponding author:
Shesnia Salim,
First Hospital of Dalian medical
University, China, China,
E-mail: dr_rishalreshin_md@hotmail.com
Received: 09 Apr 2022
Accepted: 02 May 2022
Published: 06 May 2022
J Short Name: ACMCR
Copyright:
©2022 Shesnia Salim. This is an open access article dis-
tributed under the terms of the Creative Commons Attri-
bution License, which permits unrestricted use, distribu-
tion, and build upon your work non-commercially.
Citation:
Shesnia Salim, Whole Tumor Volume Based Histogram
Analysis of ADC for Differentiating between who Grade
II and III Glioma. Ann Clin Med Case Rep.
2022; V9(2): 1-5
http://www.acmcasereport.com/ 1
1. Introduction
Accurate discrimination between high grade gliomas (HGG) and
metastatic brain tumor (MET) using noninvasive imaging is essen-
tial for selecting appropriate surgical and radiotherapy treatments
and for determining the treatment response.
2. Brain Tumors
Any uncontrolled growth of abnormal cells is called a tumor and
when located within the brain they are known as brain tumors.
They are categorized into Primary and Secondary brain tumors in
which Primary brain tumors are tumors that arise from the cells,
the meninges or neurons in the brain and Secondary tumors are
those that do not initiate in the brain. The most common prima-
ry ones are Gliomas and Meningiomas. Gliomas are derived from
glial cells such as astrocytes, oligodendrocytes, and ependymal
cells. World Health Organization (WHO) classifies gliomas into
four categories on the basis of their histologic features and malig-
nancies.
3. DWI and ADC
Brain diagnostic assay represents the gold customary for histo-
pathological diagnosing, that relies on nuclear pleomorphism,
mitotic activity, physiological condition, epithelial tissue cell mul-
tiplication and presence of gangrene [1]. This is often more and
more challenged by new non-invasive advanced techniques and
analysis nto extra sequences to enhance imaging diagnostic ac-
curacy. Image non-uniformity quantification and a lot of correct
non-invasive imaging techniques might impact patient manage-
ment by permitting a lot of tailored and customized management.
Discovering new ways which utilizes pictures that exist before
hand so that it has the ability to not only raise the standard of diag-
noses but also in addition to it, utilize scarce attention resources in
the most optimal manner. Owing to its multi-parametric approach,
MRI is visually a lot more heterogeneous than CT and should be
a strong platform to quantify neoplasm non-uniformity with ease.
MR images contain in a great amount of information on the tex-
ture properties which maybe useful for diagnosis and treatment in
clinical settings. However, MRI is not capable of producing infor-
mation at the microscopic level to be evaluated visually due to its
basic limitations in resolution qualities. Although, textural chang-
es maybe generated in MR images corresponding to the histologi-
cal changes which can be easily quantified using texture analysis.
There seems to be an inverse correlation between Apparent Dif-
fusion Coefficient (ADC) And cellularity in tumors which is mea-
sured from Diffusion Weighted Images (DWI) or DTI [2,3]. Sim-
ilarly, the use of ADC in differentiating between PCL, HGG and
METS have been demonstrated in previous studies [4,5]. The role
of diffusion-weighted (DW) magnetic resonance (MR) imaging
with Quantitative apparent diffusion coefficients (ADCs) in the
pretreatment evaluation of glioma grade has been investigated in
various studies [6-11].
4. Texture Analysis
Texture is a property that describes pictorial and volumetric as-
pects of an object two dimensionally and three-dimensionally re-
spectively. Both in nature and man-made objects, texture is ob-
served and detected qualitatively by sense of touch and vision and
described as fine, coarse, smooth, irregular or lineated depending
upon our perception. [12] However, there exists a limitation in the
http://www.acmcasereport.com/ 2
Volume 9 Issue 2 -2022 Review Article
ability of human vision to detect and differentiate complex tex-
tures [13]. Numerous parameters may be used to quantitatively
define and analyse texture using various techniques of calculation.
[14] But unfortunately, these methods also are unable to detect tex-
tural differences above the limits of human ability [15].
5. Method
Fourteen patients with low grade glioma and 47 patients with high
grade glioma were enrolled in this retrospective study in which tu-
mor grades were pathologically confirmed. All the participants un-
derwent DWI on a 3.0T whole body scanner. ROIs that contained
the entire tumor and peripheral edema were drawn in each slice
of the ADC maps. Then texture voxel wise measurements of the
entire tumor volume were obtained. Texture parameters including
the following were recorded.
1. First-order and histogram parameters include min intensity, max
intensity, mean value, median intensity, the 10th,25th,50th,75th
and 90th percentiles, range, voxel number, std deviation, variance,
relative deviation, mean deviation, skewness, kurtosis and unifor-
mity.
2.Gray level co-occurrence matrix parameters consist of energy,
entropy, inertia, correlation, inverse difference moment.
3.Gray level run length maxia parameters contains long run em-
phasis, short run emphasis, grey level nonuniformity, run length
nonuniformity.
The obtained parameters were compared between groups through
the SPSS 18.0. Using logistic regression analysis the independent
risk factors and joint variables were obtained, receiver operating
characteristic (ROC) test was used to assess the ability of indepen-
dent risk factors and joint variable between low and high grade gli-
oma. All statistical results were P<0.05 as statistically significant.
6. Results
The ADC map of typical cases of low and high grade glioma
are shown in Figure 1. The texture parameters of low and high
grade glioma and comparison results are summarized in Table 1.
It can be seen that min intensity, max intensity, median intensi-
ty, mean value, the 10th, 25th, 50th, 75th, 90th percentiles, skew-
ness, uniformity, correlation, inverse difference moment, short run
emphasis are decreased in high grade than low grade, and on the
contrary, range, voxel number, std deviation, variance, relative
deviation, mean deviation, kurtosis, energy, entropy, inertia, long
run emphasis, grey level nonuniformity, run length nonuniformity
are increased. Among all, min intensity (p=0.041), 10th percen-
tiles(p=0.003), voxel number(p=0.0001, skewness(p=0.001),
entropy(p=0.001), inverse difference moment(p=0.002), long run
emphasis(p=0.005), short run emphasis(p=0.012), run length non-
uniformity (p=0.000), showed significant difference between two
groups. Entering min intensity, 10th percentiles, voxel number,
skewness, entropy, inverse difference moment, long run emphasis,
short run emphasis, run length nonuniformity into logistic regres-
sion analysis, using step-by-step regression method it was obtained
that skewness, entropy and long run emphasis are the independent
risk factors, the prediction accuracy of logisitic regression model
is 86.9%, the regression coefficient, OR value and p value of them
are shown in Table 2. Combining all independent risk factors into
a joint variable, the ROC test showed that skewness, entropy, long
run emphasis and joint variable feature significant difference be-
tween two groups (Figure 2), The AUC, cutoff value, sensitivity
and specificity of the parameters are summarized in Table 3, and
the best parameter is joint variable, the AUC is 0.956.
http://www.acmcasereport.com/ 3
Volume 9 Issue 2 -2022 Review Article
Figure a-b: WHO grade IV,T2WI(fig.a)shows mix signal intensity in tumor,necrotic area can be seen,with edema signal. In ADC maps(fig.b) ROI
was drawn including the entire tumor and peripheral edema. Fig c-d, WHO grade II show uniform slightly higher intensity on T2WI(fig.c). In ADC
maps(fig.d), ROI was drawn along the border of uniform mass. Fig.e is the ROC curve of skewness, entropy,long run emphasis and a joint variable of
them,the AUC of them is 0.956, 0.774,0.766,0.602.
Table 1: Texture parameters of ADC signal values between low and high grade glioma.
ADC signal value texture analysis parameter Low grade(n=14) High grade(n=47) p value
Min intensity (1.22±0.42)×102 (0.85±0.59)×102 0.041#
Max intensity (2.32±0.09)×102 (2.31±0.09)×102 0.938
Median intensity (1.93±0.06)×102 (1.92±0.03)×102 0.778
Mean value (1.93±0.06)×102 (1.89±0.07)×102 0.460
10th percentiles (1.83±0.04)×102 (1.58±0.37)×102 0.003#
25th percentiles (1.87±0.07)×102 (1.84±0.16)×102 0.231
50th percentiles (1.94±0.05)×102 (1.93±0.04)×102 0.680
75th percentiles (1.94±0.07)×102 (1.94±0.04)×102 0.879
90th percentiles (2.01±0.10)×102 (2.01±0.08)×102 0.961
Range (1.11±0.47)×102 (1.46±0.62)×102 0.060
Voxel number* (5.24±2.48)×106 (1.26±0.89) ×107 0.001#
Std deviation (1.29±1.08)×101 (1.95±1.11)×101 0.208
Variance* (1.18±0.27)×102 (2.15±0.98)×102 0.208
Relative deviation (6.17±0.64)×101 (6.61±0.97)×101 0.460
Mean deviation (1.10±0.88) ×104 (2.49±1.07) ×104 0.122
Skewness* ﹣0.95±-1.53 -3.05±-5.81 0.001#
Kurtosis* 6.76±3.56 8.65±4.36 0.929
Uniformity 0.93±0.06 0.92±0.85 0.208
Energy * 0.09±0.03 0.12±0.06 0.438
Entropy 3.40±0.97 4.40±0.94 0.001#
Inertia* 2.78±1.32 4.51±2.43 0.361
Correlation* 0.18±0.04 0.11±0.06 0.395
Inverse difference moment 0.72±0.12 0.62±0.10 0.002#
Long run emphasis* 0.99±0.95 0.99±0.97 0.005#
Short run emphasis * 1.07±1.01 1.03±1.00 0.012#
Grey level nonuniformity* (1.41±0. 45) ×103 (2.28±0.95) ×103 0.294
Run length nonuniformity (2.72±1.95) ×104 (5.67±3.94) ×104 0.000#
Note: *on behalf of the nonnormal diatribution, representation with median value±interquartile.#
http://www.acmcasereport.com/ 4
Volume 9 Issue 2 -2022 Review Article
Table 2: Binary logistic regression.
Texture analysis parameter Regression coefficient OR value(95%CI) p value
Skewness -1.0017 0.362(0.123,0.062) 0.010
Entropy 1.887 6.598(5.322,32.928) 0.021
Long run emphasis 11.551 1. 039(1.004,1.108) 0.013
Table 3: ADC signal value texture parameters diagnostic ability.
ADC signal value texture parameters AUC cutoff value sensitivity specificity
Joint variance 0.956 0.804 85.1% 100%
Long run emphasis 0.774 0.990 95.7% 92.9%
Entropy 0.766 4.069 61.7% 85.7%
Skewness 0.602 -1.549 68.1% 64.3%
7. Discussion and Conclusion
Texture analysis is a new image post-processing technique, reflect
intrinsic properties include gray level statistical information, space
and structure information, besides, contains the contact with sur-
rounding environment of a given voxel [3]. Different grade glioma
has different heterogeneity, tumor parenchyma and cystic, necrosis
and hemorrhage area shows different signal on ADC maps, cause
different texture, so as to realize quantitative analysis. In this
study, min intensity and 10th percentiles showed significant dif-
ference between low and high grade glioma, suggesting that ADC
value in low zone is more meaningful. In other words, the low-
er range of ADC better reflects the progress of higher cellularity.
Standard deviation shows the level of data dispersion, higher stan-
dard deviation of ADC indicates larger regions of cystic, necrosis
or haemorrhage. Skewness describes the symmetry of the curve
distribution. Compared with low grade, the ADC value of high
grade concentrate on low zone, the center of the histogram curve
was shifted to left. Entropy and inverse difference moment reflect
gray level uniformity of image, showed significant difference be-
tween low and high grade glioma, illustrate that high grade glioma
is more nonuni form than low grade. Run emphasis reflect direc-
tion, distance and variability of texton quantitative, the long run
emphasis increase and short run emphasis decrease signifucantly
in high grade glioma compare with low grade, illustrate that high
grade contains more long run factors and less short run factors, low
grade glioma contains less long run factors and more short run fac-
tors, run length nonuniformity of high grade glioma is higher too.
Overall, it is seen that texture analysis of ADC signal value based
on entire tumor could provide more information in differentiation
of low and high grade glioma. Through logistic regression analysis
we obtain skewness, entropy, long run emphasis are the indepen-
dent risk factors, and joint application of them showed superior
diagnostic value.
References
1. Cancer Genome Atlas Research N. Comprehensive genomic char-
acterization defines human glioblastoma genes and core pathways.
Nature. 2008; 455(7216): 1061-8.
2. Guo AC, Cummings TJ, Dash RC. Lymphomas and high-grade as-
trocytomas: comparison of water diffusibility and histologic charac-
teristics. Radiology. 2002; 224(1): 177-183.
3. Yamasaki F, Kurisu K, Satoh K. Apparent diffusion coefficient of
human brain tumors at MR imaging. Radiology. 2005; 235(3): 985-
991.
4. Batra A, Tripathi RP. Atypical diffusion-weighted magnetic reso-
nance findings in glioblastoma multiforme. Australasian Radiology.
2004; 48(3): 388-391.
5. Toh CH, Chen YL, Hsieh TC. Glioblastoma multiforme with diffu-
sion-weighted magnetic resonance imaging characteristics mimick-
ing primary brain lymphoma. Case report. Journal of neurosurgery.
2006; 105(1): 132-135.
6. Sugahara T, Korogi Y, Kochi M. Usefulness of diffusion-weighted
MRI with echo-planar technique in the evaluation of cellularity in
gliomas. Journal of magnetic resonance imaging: JMRI. 1999; 9(1):
53-60.
7. Murakami R, Hirai T, Kitajima M. Magnetic resonance imaging of
pilocytic astrocytomas: usefulness of the minimum apparent diffu-
sion coefficient (ADC) value for differentiation from high-grade gli-
omas. Acta radiologica. 2008; 49(4): 462-467.
8. Provenzale JM, Mukundan S, Barboriak DP. Diffusion-weighted and
perfusion MR imaging for brain tumor characterization and assess-
ment of treatment response. Radiology. 2006; 239(3): 632-649.
9. Tozer DJ, Jager HR, Danchaivijitr N. Apparent diffusion coefficient
histograms may predict low-grade glioma subtype. NMR inbiomed-
icine. 2007; 20(1): 49-57.
10. Arvinda HR, Kesavadas C, Sarma PS. Glioma grading: sensitivity,
specificity, positive and negative predictive values of diffusion and
perfusion imaging. Journal of neuro-oncology. 2009; 94(1): 87-96.
http://www.acmcasereport.com/ 5
Volume 9 Issue 2 -2022 Review Article
11. Lee EJ, Lee SK, Agid R. Preoperative grading of presumptive low-
grade astrocytomas on MR imaging: diagnostic value of minimum
apparent diffusion coefficient. AJNR American journal of neurora-
diology. 2008; 29(10): 1872-1877.
12. Haralick RM, Shanmugam K, Dinstein I. Textural Features for Im-
age Classification. IEEE Transactions on Systems, Man, and Cyber-
netics. 1973; SMC-3(6): 610-21.
13. Julesz B, Gilbert EN, Shepp LA. Inability of humans to discriminate
between visual textures that agree in second-order statistics-revisit-
ed. Perception. 1973; 2(4): 391-405.
14. M Tuceryan and A K Jain. “Texture Analysis. The Handbook of Pat-
tern Recognition and Computer Vision (2nd Edition),” World Scien-
tific Publishing C. 1998; 207-248.
15. Harrison Lara. Clinical Applicability of MRI Texture Analysis.
16. [Doctoral thesis]. Univeristy of Tampere: Tampere University Press.
2011.

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Differentiate Low and High Grade Glioma Using ADC Maps

  • 1. Annals of Clinical and Medical Case Reports ReviewArticle ISSN 2639-8109 Volume 9 Shesnia Salim* and Padikkalakandy Cheriyath First Hospital of Dalian medical University, China Texture Analysis of Quantitative ADC Maps to Differentiate Low from High Grade Glioma * Corresponding author: Shesnia Salim, First Hospital of Dalian medical University, China, China, E-mail: dr_rishalreshin_md@hotmail.com Received: 09 Apr 2022 Accepted: 02 May 2022 Published: 06 May 2022 J Short Name: ACMCR Copyright: ©2022 Shesnia Salim. This is an open access article dis- tributed under the terms of the Creative Commons Attri- bution License, which permits unrestricted use, distribu- tion, and build upon your work non-commercially. Citation: Shesnia Salim, Whole Tumor Volume Based Histogram Analysis of ADC for Differentiating between who Grade II and III Glioma. Ann Clin Med Case Rep. 2022; V9(2): 1-5 http://www.acmcasereport.com/ 1 1. Introduction Accurate discrimination between high grade gliomas (HGG) and metastatic brain tumor (MET) using noninvasive imaging is essen- tial for selecting appropriate surgical and radiotherapy treatments and for determining the treatment response. 2. Brain Tumors Any uncontrolled growth of abnormal cells is called a tumor and when located within the brain they are known as brain tumors. They are categorized into Primary and Secondary brain tumors in which Primary brain tumors are tumors that arise from the cells, the meninges or neurons in the brain and Secondary tumors are those that do not initiate in the brain. The most common prima- ry ones are Gliomas and Meningiomas. Gliomas are derived from glial cells such as astrocytes, oligodendrocytes, and ependymal cells. World Health Organization (WHO) classifies gliomas into four categories on the basis of their histologic features and malig- nancies. 3. DWI and ADC Brain diagnostic assay represents the gold customary for histo- pathological diagnosing, that relies on nuclear pleomorphism, mitotic activity, physiological condition, epithelial tissue cell mul- tiplication and presence of gangrene [1]. This is often more and more challenged by new non-invasive advanced techniques and analysis nto extra sequences to enhance imaging diagnostic ac- curacy. Image non-uniformity quantification and a lot of correct non-invasive imaging techniques might impact patient manage- ment by permitting a lot of tailored and customized management. Discovering new ways which utilizes pictures that exist before hand so that it has the ability to not only raise the standard of diag- noses but also in addition to it, utilize scarce attention resources in the most optimal manner. Owing to its multi-parametric approach, MRI is visually a lot more heterogeneous than CT and should be a strong platform to quantify neoplasm non-uniformity with ease. MR images contain in a great amount of information on the tex- ture properties which maybe useful for diagnosis and treatment in clinical settings. However, MRI is not capable of producing infor- mation at the microscopic level to be evaluated visually due to its basic limitations in resolution qualities. Although, textural chang- es maybe generated in MR images corresponding to the histologi- cal changes which can be easily quantified using texture analysis. There seems to be an inverse correlation between Apparent Dif- fusion Coefficient (ADC) And cellularity in tumors which is mea- sured from Diffusion Weighted Images (DWI) or DTI [2,3]. Sim- ilarly, the use of ADC in differentiating between PCL, HGG and METS have been demonstrated in previous studies [4,5]. The role of diffusion-weighted (DW) magnetic resonance (MR) imaging with Quantitative apparent diffusion coefficients (ADCs) in the pretreatment evaluation of glioma grade has been investigated in various studies [6-11]. 4. Texture Analysis Texture is a property that describes pictorial and volumetric as- pects of an object two dimensionally and three-dimensionally re- spectively. Both in nature and man-made objects, texture is ob- served and detected qualitatively by sense of touch and vision and described as fine, coarse, smooth, irregular or lineated depending upon our perception. [12] However, there exists a limitation in the
  • 2. http://www.acmcasereport.com/ 2 Volume 9 Issue 2 -2022 Review Article ability of human vision to detect and differentiate complex tex- tures [13]. Numerous parameters may be used to quantitatively define and analyse texture using various techniques of calculation. [14] But unfortunately, these methods also are unable to detect tex- tural differences above the limits of human ability [15]. 5. Method Fourteen patients with low grade glioma and 47 patients with high grade glioma were enrolled in this retrospective study in which tu- mor grades were pathologically confirmed. All the participants un- derwent DWI on a 3.0T whole body scanner. ROIs that contained the entire tumor and peripheral edema were drawn in each slice of the ADC maps. Then texture voxel wise measurements of the entire tumor volume were obtained. Texture parameters including the following were recorded. 1. First-order and histogram parameters include min intensity, max intensity, mean value, median intensity, the 10th,25th,50th,75th and 90th percentiles, range, voxel number, std deviation, variance, relative deviation, mean deviation, skewness, kurtosis and unifor- mity. 2.Gray level co-occurrence matrix parameters consist of energy, entropy, inertia, correlation, inverse difference moment. 3.Gray level run length maxia parameters contains long run em- phasis, short run emphasis, grey level nonuniformity, run length nonuniformity. The obtained parameters were compared between groups through the SPSS 18.0. Using logistic regression analysis the independent risk factors and joint variables were obtained, receiver operating characteristic (ROC) test was used to assess the ability of indepen- dent risk factors and joint variable between low and high grade gli- oma. All statistical results were P<0.05 as statistically significant. 6. Results The ADC map of typical cases of low and high grade glioma are shown in Figure 1. The texture parameters of low and high grade glioma and comparison results are summarized in Table 1. It can be seen that min intensity, max intensity, median intensi- ty, mean value, the 10th, 25th, 50th, 75th, 90th percentiles, skew- ness, uniformity, correlation, inverse difference moment, short run emphasis are decreased in high grade than low grade, and on the contrary, range, voxel number, std deviation, variance, relative deviation, mean deviation, kurtosis, energy, entropy, inertia, long run emphasis, grey level nonuniformity, run length nonuniformity are increased. Among all, min intensity (p=0.041), 10th percen- tiles(p=0.003), voxel number(p=0.0001, skewness(p=0.001), entropy(p=0.001), inverse difference moment(p=0.002), long run emphasis(p=0.005), short run emphasis(p=0.012), run length non- uniformity (p=0.000), showed significant difference between two groups. Entering min intensity, 10th percentiles, voxel number, skewness, entropy, inverse difference moment, long run emphasis, short run emphasis, run length nonuniformity into logistic regres- sion analysis, using step-by-step regression method it was obtained that skewness, entropy and long run emphasis are the independent risk factors, the prediction accuracy of logisitic regression model is 86.9%, the regression coefficient, OR value and p value of them are shown in Table 2. Combining all independent risk factors into a joint variable, the ROC test showed that skewness, entropy, long run emphasis and joint variable feature significant difference be- tween two groups (Figure 2), The AUC, cutoff value, sensitivity and specificity of the parameters are summarized in Table 3, and the best parameter is joint variable, the AUC is 0.956.
  • 3. http://www.acmcasereport.com/ 3 Volume 9 Issue 2 -2022 Review Article Figure a-b: WHO grade IV,T2WI(fig.a)shows mix signal intensity in tumor,necrotic area can be seen,with edema signal. In ADC maps(fig.b) ROI was drawn including the entire tumor and peripheral edema. Fig c-d, WHO grade II show uniform slightly higher intensity on T2WI(fig.c). In ADC maps(fig.d), ROI was drawn along the border of uniform mass. Fig.e is the ROC curve of skewness, entropy,long run emphasis and a joint variable of them,the AUC of them is 0.956, 0.774,0.766,0.602. Table 1: Texture parameters of ADC signal values between low and high grade glioma. ADC signal value texture analysis parameter Low grade(n=14) High grade(n=47) p value Min intensity (1.22±0.42)×102 (0.85±0.59)×102 0.041# Max intensity (2.32±0.09)×102 (2.31±0.09)×102 0.938 Median intensity (1.93±0.06)×102 (1.92±0.03)×102 0.778 Mean value (1.93±0.06)×102 (1.89±0.07)×102 0.460 10th percentiles (1.83±0.04)×102 (1.58±0.37)×102 0.003# 25th percentiles (1.87±0.07)×102 (1.84±0.16)×102 0.231 50th percentiles (1.94±0.05)×102 (1.93±0.04)×102 0.680 75th percentiles (1.94±0.07)×102 (1.94±0.04)×102 0.879 90th percentiles (2.01±0.10)×102 (2.01±0.08)×102 0.961 Range (1.11±0.47)×102 (1.46±0.62)×102 0.060 Voxel number* (5.24±2.48)×106 (1.26±0.89) ×107 0.001# Std deviation (1.29±1.08)×101 (1.95±1.11)×101 0.208 Variance* (1.18±0.27)×102 (2.15±0.98)×102 0.208 Relative deviation (6.17±0.64)×101 (6.61±0.97)×101 0.460 Mean deviation (1.10±0.88) ×104 (2.49±1.07) ×104 0.122 Skewness* ﹣0.95±-1.53 -3.05±-5.81 0.001# Kurtosis* 6.76±3.56 8.65±4.36 0.929 Uniformity 0.93±0.06 0.92±0.85 0.208 Energy * 0.09±0.03 0.12±0.06 0.438 Entropy 3.40±0.97 4.40±0.94 0.001# Inertia* 2.78±1.32 4.51±2.43 0.361 Correlation* 0.18±0.04 0.11±0.06 0.395 Inverse difference moment 0.72±0.12 0.62±0.10 0.002# Long run emphasis* 0.99±0.95 0.99±0.97 0.005# Short run emphasis * 1.07±1.01 1.03±1.00 0.012# Grey level nonuniformity* (1.41±0. 45) ×103 (2.28±0.95) ×103 0.294 Run length nonuniformity (2.72±1.95) ×104 (5.67±3.94) ×104 0.000# Note: *on behalf of the nonnormal diatribution, representation with median value±interquartile.#
  • 4. http://www.acmcasereport.com/ 4 Volume 9 Issue 2 -2022 Review Article Table 2: Binary logistic regression. Texture analysis parameter Regression coefficient OR value(95%CI) p value Skewness -1.0017 0.362(0.123,0.062) 0.010 Entropy 1.887 6.598(5.322,32.928) 0.021 Long run emphasis 11.551 1. 039(1.004,1.108) 0.013 Table 3: ADC signal value texture parameters diagnostic ability. ADC signal value texture parameters AUC cutoff value sensitivity specificity Joint variance 0.956 0.804 85.1% 100% Long run emphasis 0.774 0.990 95.7% 92.9% Entropy 0.766 4.069 61.7% 85.7% Skewness 0.602 -1.549 68.1% 64.3% 7. Discussion and Conclusion Texture analysis is a new image post-processing technique, reflect intrinsic properties include gray level statistical information, space and structure information, besides, contains the contact with sur- rounding environment of a given voxel [3]. Different grade glioma has different heterogeneity, tumor parenchyma and cystic, necrosis and hemorrhage area shows different signal on ADC maps, cause different texture, so as to realize quantitative analysis. In this study, min intensity and 10th percentiles showed significant dif- ference between low and high grade glioma, suggesting that ADC value in low zone is more meaningful. In other words, the low- er range of ADC better reflects the progress of higher cellularity. Standard deviation shows the level of data dispersion, higher stan- dard deviation of ADC indicates larger regions of cystic, necrosis or haemorrhage. Skewness describes the symmetry of the curve distribution. Compared with low grade, the ADC value of high grade concentrate on low zone, the center of the histogram curve was shifted to left. Entropy and inverse difference moment reflect gray level uniformity of image, showed significant difference be- tween low and high grade glioma, illustrate that high grade glioma is more nonuni form than low grade. Run emphasis reflect direc- tion, distance and variability of texton quantitative, the long run emphasis increase and short run emphasis decrease signifucantly in high grade glioma compare with low grade, illustrate that high grade contains more long run factors and less short run factors, low grade glioma contains less long run factors and more short run fac- tors, run length nonuniformity of high grade glioma is higher too. Overall, it is seen that texture analysis of ADC signal value based on entire tumor could provide more information in differentiation of low and high grade glioma. Through logistic regression analysis we obtain skewness, entropy, long run emphasis are the indepen- dent risk factors, and joint application of them showed superior diagnostic value. References 1. Cancer Genome Atlas Research N. Comprehensive genomic char- acterization defines human glioblastoma genes and core pathways. Nature. 2008; 455(7216): 1061-8. 2. Guo AC, Cummings TJ, Dash RC. Lymphomas and high-grade as- trocytomas: comparison of water diffusibility and histologic charac- teristics. Radiology. 2002; 224(1): 177-183. 3. Yamasaki F, Kurisu K, Satoh K. Apparent diffusion coefficient of human brain tumors at MR imaging. Radiology. 2005; 235(3): 985- 991. 4. Batra A, Tripathi RP. Atypical diffusion-weighted magnetic reso- nance findings in glioblastoma multiforme. Australasian Radiology. 2004; 48(3): 388-391. 5. Toh CH, Chen YL, Hsieh TC. Glioblastoma multiforme with diffu- sion-weighted magnetic resonance imaging characteristics mimick- ing primary brain lymphoma. Case report. Journal of neurosurgery. 2006; 105(1): 132-135. 6. Sugahara T, Korogi Y, Kochi M. Usefulness of diffusion-weighted MRI with echo-planar technique in the evaluation of cellularity in gliomas. Journal of magnetic resonance imaging: JMRI. 1999; 9(1): 53-60. 7. Murakami R, Hirai T, Kitajima M. Magnetic resonance imaging of pilocytic astrocytomas: usefulness of the minimum apparent diffu- sion coefficient (ADC) value for differentiation from high-grade gli- omas. Acta radiologica. 2008; 49(4): 462-467. 8. Provenzale JM, Mukundan S, Barboriak DP. Diffusion-weighted and perfusion MR imaging for brain tumor characterization and assess- ment of treatment response. Radiology. 2006; 239(3): 632-649. 9. Tozer DJ, Jager HR, Danchaivijitr N. Apparent diffusion coefficient histograms may predict low-grade glioma subtype. NMR inbiomed- icine. 2007; 20(1): 49-57. 10. Arvinda HR, Kesavadas C, Sarma PS. Glioma grading: sensitivity, specificity, positive and negative predictive values of diffusion and perfusion imaging. Journal of neuro-oncology. 2009; 94(1): 87-96.
  • 5. http://www.acmcasereport.com/ 5 Volume 9 Issue 2 -2022 Review Article 11. Lee EJ, Lee SK, Agid R. Preoperative grading of presumptive low- grade astrocytomas on MR imaging: diagnostic value of minimum apparent diffusion coefficient. AJNR American journal of neurora- diology. 2008; 29(10): 1872-1877. 12. Haralick RM, Shanmugam K, Dinstein I. Textural Features for Im- age Classification. IEEE Transactions on Systems, Man, and Cyber- netics. 1973; SMC-3(6): 610-21. 13. Julesz B, Gilbert EN, Shepp LA. Inability of humans to discriminate between visual textures that agree in second-order statistics-revisit- ed. Perception. 1973; 2(4): 391-405. 14. M Tuceryan and A K Jain. “Texture Analysis. The Handbook of Pat- tern Recognition and Computer Vision (2nd Edition),” World Scien- tific Publishing C. 1998; 207-248. 15. Harrison Lara. Clinical Applicability of MRI Texture Analysis. 16. [Doctoral thesis]. Univeristy of Tampere: Tampere University Press. 2011.