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Grading of Gliomas by Using Monoexponential, Biexponential, and Stretched Exponential Diffusion-weighted MR Imaging and Diffusion Kurtosis MR Imaging

Overview
Journal Radiology
Specialty Radiology
Date 2015 Aug 1
PMID 26230975
Citations 97
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Abstract

Purpose: To quantitatively compare the potential of various diffusion parameters obtained from monoexponential, biexponential, and stretched exponential diffusion-weighted imaging models and diffusion kurtosis imaging in the grading of gliomas.

Materials And Methods: This study was approved by the local ethics committee, and written informed consent was obtained from all subjects. Both diffusion-weighted imaging and diffusion kurtosis imaging were performed in 69 patients with pathologically proven gliomas by using a 3-T magnetic resonance (MR) imaging unit. An isotropic apparent diffusion coefficient (ADC), true ADC, pseudo-ADC, and perfusion fraction were calculated from diffusion-weighted images by using a biexponential model. A water molecular diffusion heterogeneity index and distributed diffusion coefficient were calculated from diffusion-weighted images by using a stretched exponential model. Mean diffusivity, fractional anisotropy, and mean kurtosis were calculated from diffusion kurtosis images. All values were compared between high-grade and low-grade gliomas by using a Mann-Whitney U test. Receiver operating characteristic and Spearman rank correlation analysis were used for statistical evaluations.

Results: ADC, true ADC, perfusion fraction, water molecular diffusion heterogeneity index, distributed diffusion coefficient, and mean diffusivity values were significantly lower in high-grade gliomas than in low-grade gliomas (U = 109, 56, 129, 6, 206, and 229, respectively; P < .05). Pseudo-ADC and mean kurtosis values were significantly higher in high-grade gliomas than in low-grade gliomas (U = 98 and 8, respectively; P < .05). Both water molecular diffusion heterogeneity index (area under the receiver operating characteristic curve [AUC] = 0.993) and mean kurtosis (AUC = 0.991) had significantly greater AUC values than ADC (AUC = 0.866), mean diffusivity (AUC = 0.722), and fractional anisotropy (AUC = 0.500) in the differentiation of low-grade and high-grade gliomas (P < .05).

Conclusion: Water molecular diffusion heterogeneity index and mean kurtosis values may provide additional information and improve the grading of gliomas compared with conventional diffusion parameters.

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References
1.
Sehy J, Zhao L, Xu J, Rayala H, Ackerman J, Neil J . Effects of physiologic challenge on the ADC of intracellular water in the Xenopus oocyte. Magn Reson Med. 2004; 52(2):239-47. DOI: 10.1002/mrm.20132. View

2.
Jones D . The effect of gradient sampling schemes on measures derived from diffusion tensor MRI: a Monte Carlo study. Magn Reson Med. 2004; 51(4):807-15. DOI: 10.1002/mrm.20033. View

3.
Le Bihan D, Breton E, lAllemand D, Grenier P, Cabanis E, LAVAL-JEANTET M . MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders. Radiology. 1986; 161(2):401-7. DOI: 10.1148/radiology.161.2.3763909. View

4.
Le Bihan D, Breton E, lAllemand D, Aubin M, VIGNAUD J, LAVAL-JEANTET M . Separation of diffusion and perfusion in intravoxel incoherent motion MR imaging. Radiology. 1988; 168(2):497-505. DOI: 10.1148/radiology.168.2.3393671. View

5.
Sugahara T, Korogi Y, Kochi M, Ikushima I, SHIGEMATU Y, Hirai T . Usefulness of diffusion-weighted MRI with echo-planar technique in the evaluation of cellularity in gliomas. J Magn Reson Imaging. 1999; 9(1):53-60. DOI: 10.1002/(sici)1522-2586(199901)9:1<53::aid-jmri7>3.0.co;2-2. View