Diffusion kurtosis imaging and diffusion-weighted imaging in assessment of liver fibrosis stage and necroinflammatory activity.

Purpose: To investigate and compare the diagnostic value of diffusion kurtosis imaging (DKI) with diffusion-weighted imaging (DWI) in assessing and quantifying hepatic fibrosis. Methods: Thirty rats were divided into the control group ( n = 6) and the fibrosis experimental groups ( n = 6 per group)...

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Publicado en:Abdominal Radiology Vol. 42; no. 4; pp. 1176 - 1183
Autores principales: Sheng, Ruo, Wang, He, Yang, Li, Jin, Kai, Xie, Yan, Chen, Cai, Zeng, Meng
Formato: Journal Article
Publicado: Springer Nature Apr2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Apr2017
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00261-016-0984-4
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        atl: Diffusion kurtosis imaging and diffusion-weighted imaging in assessment of liver fibrosis stage and necroinflammatory activity.
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        au:
          Sheng, Ruo
          Wang, He
          Yang, Li
          Jin, Kai
          Xie, Yan
          Chen, Cai
          Zeng, Meng
        affil: Department of Radiology, Zhongshan Hospital , Fudan University, Shanghai Institute of Medical Imaging , No. 180 Fenglin Road, Xuhui District Shanghai 200032 China
      sug:
      ab: Purpose: To investigate and compare the diagnostic value of diffusion kurtosis imaging (DKI) with diffusion-weighted imaging (DWI) in assessing and quantifying hepatic fibrosis. Methods: Thirty rats were divided into the control group ( n = 6) and the fibrosis experimental groups ( n = 6 per group) with CCl administration for 2, 4, 6, and 8 weeks. Liver fibrosis stage (S) and necroinflammatory activity grade (G) were histopathologically determined. DKI and DWI were performed; mean apparent diffusion (MD), mean kurtosis (MK), and apparent diffusion coefficient (ADC) values were calculated. DKI parameters were compared with ADC values according to G/S scores. Results: Strong inverse correlations were found between the degree of fibrosis and both MD and ADC ( r = −0.840 and r = −0.760), while only weak correlation existed in MK ( r = 0.405). ROC analyses demonstrated the AUC in MD, MK, and ADC of 0.862, 0.684, 0.817 for identifying mild and severe fibrosis, and 0.757, 0.675, 0.733 for non-cirrhosis and cirrhosis, respectively. The degree of fibrosis was significantly correlated with α-smooth muscle actin (α-SMA) ( P < 0.0001); α-SMA had strong inverse correlation with MD ( r = −0.723), moderate inverse correlation with ADC ( r = −0.613), and very weak correlation with MK ( r = 0.175). Additionally, MD was strongly correlated with the necroinflammatory activity ( r = −0.758), ADC was moderately correlated ( r = −0.492), and MK was weakly correlated ( r = 0.254). Conclusion: DKI may provide added information and serve as a valuable tool for the characterization and surveillance of liver fibrosis in a non-invasive manner.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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