Diagnostic Performance of Magnetic Resonance Elastography in Staging Liver Fibrosis: A Systematic Review and Meta-analysis of Individual Participant Data
Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD). Thro...
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Published in | Clinical gastroenterology and hepatology Vol. 13; no. 3; pp. 440 - 451.e6 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.03.2015
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Subjects | |
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Abstract | Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD).
Through a systematic literature search of multiple databases (2003–2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant’s age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4).
We analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m2; 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76–0.92), 0.88 (0.84–0.91), 0.93 (0.90–0.95), and 0.92 (0.90–0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%.
Based on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE. |
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AbstractList | Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD).BACKGROUND & AIMSMagnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD).Through a systematic literature search of multiple databases (2003-2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant's age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4).METHODSThrough a systematic literature search of multiple databases (2003-2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant's age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4).We analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m(2); 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76-0.92), 0.88 (0.84-0.91), 0.93 (0.90-0.95), and 0.92 (0.90-0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%.RESULTSWe analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m(2); 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76-0.92), 0.88 (0.84-0.91), 0.93 (0.90-0.95), and 0.92 (0.90-0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%.Based on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE.CONCLUSIONSBased on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE. Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD). Through a systematic literature search of multiple databases (2003-2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant's age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4). We analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m(2); 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76-0.92), 0.88 (0.84-0.91), 0.93 (0.90-0.95), and 0.92 (0.90-0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%. Based on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE. Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD). Through a systematic literature search of multiple databases (2003–2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant’s age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4). We analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m2; 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76–0.92), 0.88 (0.84–0.91), 0.93 (0.90–0.95), and 0.92 (0.90–0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%. Based on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE. Background & AimsMagnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected from published studies to assess the diagnostic accuracy of MRE for staging liver fibrosis in patients with chronic liver diseases (CLD). MethodsThrough a systematic literature search of multiple databases (2003–2013), we identified studies on diagnostic performance of MRE for staging liver fibrosis in patients with CLD with native anatomy, using liver biopsy as the standard. We contacted study authors to collect data on each participant’s age, sex, body mass index (BMI), liver stiffness (measured by MRE), fibrosis stage, staging system used, degree of inflammation, etiology of CLD, and interval between MRE and biopsy. Through a pooled analysis, we calculated cluster-adjusted area under the receiver-operating curve, sensitivity, and specificity of MRE for any fibrosis (≥stage 1), significant fibrosis (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis (stage 4). ResultsWe analyzed data from 12 retrospective studies, comprising 697 patients (mean age, 55 ± 13 y; 59.4% male; mean BMI, 26.9 ± 6.7 kg/m 2; 92.1% with <1 year interval between MRE and biopsy; and 47.1% with hepatitis C). Overall, 19.5%, 19.4%, 15.5%, 15.9%, and 29.7% patients had stage 0, 1, 2, 3, and 4 fibrosis, respectively. The mean area under the receiver-operating curve values (and 95% confidence intervals) for the diagnosis of any (≥stage 1), significant (≥stage 2), advanced fibrosis (≥stage 3), and cirrhosis, were as follows: 0.84 (0.76–0.92), 0.88 (0.84–0.91), 0.93 (0.90–0.95), and 0.92 (0.90–0.94), respectively. A similar diagnostic performance was observed in stratified analysis based on sex, obesity, and etiology of CLD. The overall rate of failure of MRE was 4.3%. ConclusionsBased on a pooled analysis of data from individual participants, MRE has a high accuracy for the diagnosis of significant or advanced fibrosis and cirrhosis, independent of BMI and etiology of CLD. Prospective studies are warranted to better understand the diagnostic performance of MRE. |
Author | Motosugi, Utaroh Wang, Zhen Asbach, Patrick Chen, Jun Godfrey, Edmund M. Ehman, Richard L. Bridges, Mellena Lomas, David J. Hassanein, Tarek Venkatesh, Sudhakar K. Yin, Meng Low, Russell N. Singh, Siddharth Keaveny, Andrew P. Bohte, Anneloes Talwalkar, Jayant A. Miller, Frank H. Murad, Mohammad Hassan |
AuthorAffiliation | 3 Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN 9 Department of Radiology, Addenbrooke’s Hospital, Cambridge, U.K 5 Department of Radiology University of Yamanashi, Chuo-shi, Yamanashi, Japan 4 Department of Radiology, Northwestern University Feinberg School of Medicine, Chicago, IL 7 Liver Centers of Southern California, Coronado, CA 11 Department of Radiology, Department of Medicine, Mayo Clinic, Jacksonville, FL 8 Department of Radiology, Charité-Universitätsmedizin Berlin, Charité Campus Mitte, Berlin, Germany 10 Department of Transplant, Mayo Clinic, Jacksonville, FL 6 Sharp and Children’s MRI Center, San Diego, CA 1 Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN 2 Department of Radiology, Mayo Clinic, Rochester, MN 12 Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands |
AuthorAffiliation_xml | – name: 2 Department of Radiology, Mayo Clinic, Rochester, MN – name: 3 Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN – name: 12 Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands – name: 6 Sharp and Children’s MRI Center, San Diego, CA – name: 11 Department of Radiology, Department of Medicine, Mayo Clinic, Jacksonville, FL – name: 9 Department of Radiology, Addenbrooke’s Hospital, Cambridge, U.K – name: 8 Department of Radiology, Charité-Universitätsmedizin Berlin, Charité Campus Mitte, Berlin, Germany – name: 1 Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN – name: 4 Department of Radiology, Northwestern University Feinberg School of Medicine, Chicago, IL – name: 7 Liver Centers of Southern California, Coronado, CA – name: 10 Department of Transplant, Mayo Clinic, Jacksonville, FL – name: 5 Department of Radiology University of Yamanashi, Chuo-shi, Yamanashi, Japan |
Author_xml | – sequence: 1 givenname: Siddharth surname: Singh fullname: Singh, Siddharth organization: Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota – sequence: 2 givenname: Sudhakar K. surname: Venkatesh fullname: Venkatesh, Sudhakar K. email: venkatesh.sudhakar@mayo.edu organization: Department of Radiology, Mayo Clinic, Rochester, Minnesota – sequence: 3 givenname: Zhen surname: Wang fullname: Wang, Zhen organization: Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota – sequence: 4 givenname: Frank H. surname: Miller fullname: Miller, Frank H. organization: Department of Radiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois – sequence: 5 givenname: Utaroh surname: Motosugi fullname: Motosugi, Utaroh organization: Department of Radiology, University of Yamanashi, Chuo-shi, Yamanashi, Japan – sequence: 6 givenname: Russell N. surname: Low fullname: Low, Russell N. organization: Sharp and Children’s Magnetic Resonance Imaging Center, San Diego, California – sequence: 7 givenname: Tarek surname: Hassanein fullname: Hassanein, Tarek organization: Liver Centers of Southern California, Coronado, California – sequence: 8 givenname: Patrick surname: Asbach fullname: Asbach, Patrick organization: Department of Radiology, Charité-Universitätsmedizin Berlin, Charité Campus Mitte, Berlin, Germany – sequence: 9 givenname: Edmund M. surname: Godfrey fullname: Godfrey, Edmund M. organization: Department of Radiology, Addenbrooke's Hospital, Cambridge, United Kingdom – sequence: 10 givenname: Meng surname: Yin fullname: Yin, Meng organization: Department of Radiology, Mayo Clinic, Rochester, Minnesota – sequence: 11 givenname: Jun surname: Chen fullname: Chen, Jun organization: Department of Radiology, Mayo Clinic, Rochester, Minnesota – sequence: 12 givenname: Andrew P. surname: Keaveny fullname: Keaveny, Andrew P. organization: Department of Transplant, Mayo Clinic, Jacksonville, Florida – sequence: 13 givenname: Mellena surname: Bridges fullname: Bridges, Mellena organization: Department of Radiology, Department of Medicine, Mayo Clinic, Jacksonville, Florida – sequence: 14 givenname: Anneloes surname: Bohte fullname: Bohte, Anneloes organization: Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands – sequence: 15 givenname: Mohammad Hassan surname: Murad fullname: Murad, Mohammad Hassan organization: Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota – sequence: 16 givenname: David J. surname: Lomas fullname: Lomas, David J. organization: Department of Radiology, Addenbrooke's Hospital, Cambridge, United Kingdom – sequence: 17 givenname: Jayant A. surname: Talwalkar fullname: Talwalkar, Jayant A. organization: Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota – sequence: 18 givenname: Richard L. surname: Ehman fullname: Ehman, Richard L. organization: Department of Radiology, Mayo Clinic, Rochester, Minnesota |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25305349$$D View this record in MEDLINE/PubMed |
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Snippet | Magnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant data collected... Background & AimsMagnetic resonance elastography (MRE) is a noninvasive tool for staging liver fibrosis. We conducted a meta-analysis of individual participant... |
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SubjectTerms | Adult Aged Biopsy Diagnostic Performance Elasticity Imaging Techniques - methods Elastography Female Gastroenterology and Hepatology Histocytochemistry Humans IPD Liver - diagnostic imaging Liver - pathology Liver Cirrhosis - diagnosis Male Middle Aged Noninvasive Pooled Analysis ROC Curve Sensitivity and Specificity |
Title | Diagnostic Performance of Magnetic Resonance Elastography in Staging Liver Fibrosis: A Systematic Review and Meta-analysis of Individual Participant Data |
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