Assessment of Chronic Hepatitis and Fibrosis: Comparison of MR Elastography and Diffusion-Weighted Imaging
The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases. Seventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severitie...
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Published in | American journal of roentgenology (1976) Vol. 196; no. 3; pp. 553 - 561 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Reston, VA
American Roentgen Ray Society
01.03.2011
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Subjects | |
Online Access | Get full text |
ISSN | 0361-803X 1546-3141 1546-3141 |
DOI | 10.2214/AJR.10.4580 |
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Abstract | The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases.
Seventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severities of liver fibrosis and chronic hepatitis were graded by histopathologic analysis according to standard disease-specific classifications. The overall predictive ability of MRE and DWI in assessment of fibrosis was compared by constructing a receiver operating characteristic (ROC) curve and calculating the area under the curve (AUC) on the basis of histopathologic analysis.
Using ROC analysis, MRE showed greater capability than DWI in discriminating stage 2 or greater (≥ F2), stage 3 or greater (≥ F3), and cirrhosis (≥ F4), shown as significant differences in AUC (p = 0.003, p = 0.001, and p = 0.001, respectively). Higher sensitivity and specificity were shown by MRE in predicting fibrosis scores ≥ F2 (91% and 97%), scores ≥ F3 (92% and 95%), and scores F4 (95% and 87%) compared with DWI (84% and 82%, 88% and 76%, and 85% and 68%, respectively). Although MRE had higher ability in identification of liver with fibrosis scores ≥ F1 than DWI, a significant difference was not seen (p = 0.398). Stiffness values on MRE increased in relation to increasing severity of fibrosis confirmed by histopathology scores; however, a consistent relationship between apparent diffusion coefficient (ADC) values and stage of fibrosis was not shown. In addition, liver tissue with chronic hepatitis preceding fibrosis may account for mild elevation of liver stiffness.
MRE had greater predictive ability in distinguishing the stages of liver fibrosis than DWI. |
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AbstractList | The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases.OBJECTIVEThe purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases.Seventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severities of liver fibrosis and chronic hepatitis were graded by histopathologic analysis according to standard disease-specific classifications. The overall predictive ability of MRE and DWI in assessment of fibrosis was compared by constructing a receiver operating characteristic (ROC) curve and calculating the area under the curve (AUC) on the basis of histopathologic analysis.SUBJECTS AND METHODSSeventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severities of liver fibrosis and chronic hepatitis were graded by histopathologic analysis according to standard disease-specific classifications. The overall predictive ability of MRE and DWI in assessment of fibrosis was compared by constructing a receiver operating characteristic (ROC) curve and calculating the area under the curve (AUC) on the basis of histopathologic analysis.Using ROC analysis, MRE showed greater capability than DWI in discriminating stage 2 or greater (≥ F2), stage 3 or greater (≥ F3), and cirrhosis (≥ F4), shown as significant differences in AUC (p = 0.003, p = 0.001, and p = 0.001, respectively). Higher sensitivity and specificity were shown by MRE in predicting fibrosis scores ≥ F2 (91% and 97%), scores ≥ F3 (92% and 95%), and scores F4 (95% and 87%) compared with DWI (84% and 82%, 88% and 76%, and 85% and 68%, respectively). Although MRE had higher ability in identification of liver with fibrosis scores ≥ F1 than DWI, a significant difference was not seen (p = 0.398). Stiffness values on MRE increased in relation to increasing severity of fibrosis confirmed by histopathology scores; however, a consistent relationship between apparent diffusion coefficient (ADC) values and stage of fibrosis was not shown. In addition, liver tissue with chronic hepatitis preceding fibrosis may account for mild elevation of liver stiffness.RESULTSUsing ROC analysis, MRE showed greater capability than DWI in discriminating stage 2 or greater (≥ F2), stage 3 or greater (≥ F3), and cirrhosis (≥ F4), shown as significant differences in AUC (p = 0.003, p = 0.001, and p = 0.001, respectively). Higher sensitivity and specificity were shown by MRE in predicting fibrosis scores ≥ F2 (91% and 97%), scores ≥ F3 (92% and 95%), and scores F4 (95% and 87%) compared with DWI (84% and 82%, 88% and 76%, and 85% and 68%, respectively). Although MRE had higher ability in identification of liver with fibrosis scores ≥ F1 than DWI, a significant difference was not seen (p = 0.398). Stiffness values on MRE increased in relation to increasing severity of fibrosis confirmed by histopathology scores; however, a consistent relationship between apparent diffusion coefficient (ADC) values and stage of fibrosis was not shown. In addition, liver tissue with chronic hepatitis preceding fibrosis may account for mild elevation of liver stiffness.MRE had greater predictive ability in distinguishing the stages of liver fibrosis than DWI.CONCLUSIONMRE had greater predictive ability in distinguishing the stages of liver fibrosis than DWI. The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases. Seventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severities of liver fibrosis and chronic hepatitis were graded by histopathologic analysis according to standard disease-specific classifications. The overall predictive ability of MRE and DWI in assessment of fibrosis was compared by constructing a receiver operating characteristic (ROC) curve and calculating the area under the curve (AUC) on the basis of histopathologic analysis. Using ROC analysis, MRE showed greater capability than DWI in discriminating stage 2 or greater (≥ F2), stage 3 or greater (≥ F3), and cirrhosis (≥ F4), shown as significant differences in AUC (p = 0.003, p = 0.001, and p = 0.001, respectively). Higher sensitivity and specificity were shown by MRE in predicting fibrosis scores ≥ F2 (91% and 97%), scores ≥ F3 (92% and 95%), and scores F4 (95% and 87%) compared with DWI (84% and 82%, 88% and 76%, and 85% and 68%, respectively). Although MRE had higher ability in identification of liver with fibrosis scores ≥ F1 than DWI, a significant difference was not seen (p = 0.398). Stiffness values on MRE increased in relation to increasing severity of fibrosis confirmed by histopathology scores; however, a consistent relationship between apparent diffusion coefficient (ADC) values and stage of fibrosis was not shown. In addition, liver tissue with chronic hepatitis preceding fibrosis may account for mild elevation of liver stiffness. MRE had greater predictive ability in distinguishing the stages of liver fibrosis than DWI. OBJECTIVE: The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic hepatitis in patients with chronic liver diseases. SUBJECTS AND METHODS. Seventy-six patients with chronic liver disease underwent abdominal MRI, MRE, and DWI. Severities of liver fibrosis and chronic hepatitis were graded by histopathologic analysis according to standard disease-specific classifications. The overall predictive ability of MRE and DWI in assessment of fibrosis was compared by constructing a receiver operating characteristic (ROC) curve and calculating the area under the curve (AUC) on the basis of histopathologic analysis. RESULTS: Using ROC analysis, MRE showed greater capability than DWI in discriminating stage 2 or greater ( greater than or equal to F2), stage 3 or greater ( greater than or equal to F3), and cirrhosis ( greater than or equal to F4), shown as significant differences in AUC (p = 0.003, p = 0.001, and p = 0.001, respectively). Higher sensitivity and specificity were shown by MRE in predicting fibrosis scores greater than or equal to F2 (91% and 97%), scores greater than or equal to F3 (92% and 95%), and scores F4 (95% and 87%) compared with DWI (84% and 82%, 88% and 76%, and 85% and 68%, respectively). Although MRE had higher ability in identification of liver with fibrosis scores greater than or equal to F1 than DWI, a significant difference was not seen (p = 0.398). Stiffness values on MRE increased in relation to increasing severity of fibrosis confirmed by histopathology scores; however, a consistent relationship between apparent diffusion coefficient (ADC) values and stage of fibrosis was not shown. In addition, liver tissue with chronic hepatitis preceding fibrosis may account for mild elevation of liver stiffness. CONCLUSION: MRE had greater predictive ability in distinguishing the stages of liver fibrosis than DWI. |
Author | Ganger, Daniel R. Bolster, Bradley McCarthy, Robert J. Omary, Reed A. Ehman, Richard L. Levitsky, Josh Wang, Yi Shah, Saurabh Sternick, Laura A. Fasanati, Charles W. Zuehlsdorff, Sven Chen, Zongming E. Miller, Frank H. |
Author_xml | – sequence: 1 givenname: Yi surname: Wang fullname: Wang, Yi organization: Department of Radiology, Northwestern University Feinberg School of Medicine, 676 N St. Clair, Ste. 800, Chicago, IL 60611 – sequence: 2 givenname: Daniel R. surname: Ganger fullname: Ganger, Daniel R. organization: Department of Medicine, Hepatology Division, Northwestern University Feinberg School of Medicine, Chicago, IL – sequence: 3 givenname: Josh surname: Levitsky fullname: Levitsky, Josh organization: Department of Medicine, Hepatology Division, Northwestern University Feinberg School of Medicine, Chicago, IL – sequence: 4 givenname: Laura A. surname: Sternick fullname: Sternick, Laura A. organization: Department of Radiology, Northwestern University Feinberg School of Medicine, 676 N St. Clair, Ste. 800, Chicago, IL 60611 – sequence: 5 givenname: Robert J. surname: McCarthy fullname: McCarthy, Robert J. organization: Department of Anesthesiology, Northwestern University Feinberg School of Medicine, Chicago, IL – sequence: 6 givenname: Zongming E. surname: Chen fullname: Chen, Zongming E. organization: Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL – sequence: 7 givenname: Charles W. surname: Fasanati fullname: Fasanati, Charles W. organization: Department of Radiology, Northwestern University Feinberg School of Medicine, 676 N St. Clair, Ste. 800, Chicago, IL 60611 – sequence: 8 givenname: Bradley surname: Bolster fullname: Bolster, Bradley organization: Siemens Healthcare, Rochester, MN – sequence: 9 givenname: Saurabh surname: Shah fullname: Shah, Saurabh organization: Siemens Healthcare, Chicago, IL – sequence: 10 givenname: Sven surname: Zuehlsdorff fullname: Zuehlsdorff, Sven organization: Siemens Healthcare, Chicago, IL – sequence: 11 givenname: Reed A. surname: Omary fullname: Omary, Reed A. organization: Department of Radiology, Northwestern University Feinberg School of Medicine, 676 N St. Clair, Ste. 800, Chicago, IL 60611 – sequence: 12 givenname: Richard L. surname: Ehman fullname: Ehman, Richard L. organization: Department of Radiology, Mayo Clinic, Rochester, MN – sequence: 13 givenname: Frank H. surname: Miller fullname: Miller, Frank H. organization: Department of Radiology, Northwestern University Feinberg School of Medicine, 676 N St. Clair, Ste. 800, Chicago, IL 60611 |
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Keywords | Digestive system Liver Hepatic disease Nuclear magnetic resonance imaging Hepatitis Chronic Magnetic resonance elastography chronic hepatitis diffusion-weighted imaging (DWI) Fibrosis Medical imagery Digestive diseases MR elastography (MRE) Comparative study |
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Snippet | The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and chronic... OBJECTIVE: The purpose of our study was to compare the utility of MR elastography (MRE) and diffusion-weighted imaging (DWI) in characterizing fibrosis and... |
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SubjectTerms | Adult Aged Biological and medical sciences Cirrhosis Classification Contrast Media Diffusion coefficient Diffusion Magnetic Resonance Imaging Elasticity Imaging Techniques - methods Female Fibrosis Gadolinium DTPA Gastroenterology. Liver. Pancreas. Abdomen Hepatitis Hepatitis, Chronic - diagnosis Hepatitis, Chronic - pathology Humans Liver Cirrhosis - diagnosis Liver Cirrhosis - pathology Liver diseases Liver. Biliary tract. Portal circulation. Exocrine pancreas Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Medical sciences Middle Aged Other diseases. Semiology Predictive Value of Tests Prospective Studies ROC Curve Sensitivity and Specificity Statistics, Nonparametric |
Title | Assessment of Chronic Hepatitis and Fibrosis: Comparison of MR Elastography and Diffusion-Weighted Imaging |
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