Evaluation of liver fibrosis with a monoexponential model of intravoxel incoherent motion magnetic resonance imaging
To evaluate hepatic fibrosis with a monoexponential model of intravoxel incoherent motion magnetic resonance imaging, and assess the potential application value of intravoxel incoherent motion (IVIM) in diffusion-weighted imaging (IVIM-DWI) in determining staging of liver fibrosis. 28 patients with...
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Veröffentlicht in: | Oncotarget 2018-05, Vol.9 (37), p.24619-24626 |
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Sprache: | eng |
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Zusammenfassung: | To evaluate hepatic fibrosis with a monoexponential model of intravoxel incoherent motion magnetic resonance imaging, and assess the potential application value of intravoxel incoherent motion (IVIM) in diffusion-weighted imaging (IVIM-DWI) in determining staging of liver fibrosis. 28 patients with hepatic fibrosis and 25 volunteers with healthy livers had IVIM examination and conventional MRI. All standard apparent diffusion coefficient (ADC) values of IVIM raw data were post-processed off-line after completion of data collection. All regions of interest (ROIs) were manually positioned by two experienced radiologists. All values of the different fibrosis stages in the study group were compared using independent sample
tests. Using ROC analysis, both AUC values of ADC
and ADC
from study and control group were found to be between 0.8 and 1 for staging fibrosis. The mean ADC
and ADC
values of the liver in the study group were significantly lower than the values in the control group (
< 0.05). Spearman rho correlation analysis was used to determine the relationship among fibrosis stages and the ADC
and ADC
in the study group. As the stage of the fibrosis increased, the values decreased. Significant differences between the two subgroups of liver fibrosis stages were found (
< 0.05). The monoexponential model of IVIM-DWI adopted multiple
values for quantitative analysis of the water molecules diffused in the tissue. It could be used as a noninvasive and valuable method for assessment of liver fibrosis. |
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ISSN: | 1949-2553 1949-2553 |
DOI: | 10.18632/oncotarget.24758 |