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Assessment of hepatic fibrosis and inflammation with look-locker T1 mapping and magnetic resonance elastography with histopathology as reference standard

Purpose To compare the diagnostic performance of T1 mapping and MR elastography (MRE) for staging of hepatic fibrosis and grading inflammation with histopathology as standard of reference. Methods 68 patients with various liver diseases undergoing liver biopsy for suspected fibrosis or with an estab...

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Published in:Abdominal imaging 2022-11, Vol.47 (11), p.3746-3757
Main Authors: von Ulmenstein, Sophie, Bogdanovic, Sanja, Honcharova-Biletska, Hanna, Blümel, Sena, Deibel, Ansgar R., Segna, Daniel, Jüngst, Christoph, Weber, Achim, Kuntzen, Thomas, Gubler, Christoph, Reiner, Cäcilia S.
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cited_by cdi_FETCH-LOGICAL-c404t-3319589392a896b76c1ee50a2d2226b59087a14017f29998d7f8286e656389843
cites cdi_FETCH-LOGICAL-c404t-3319589392a896b76c1ee50a2d2226b59087a14017f29998d7f8286e656389843
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container_issue 11
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container_title Abdominal imaging
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creator von Ulmenstein, Sophie
Bogdanovic, Sanja
Honcharova-Biletska, Hanna
Blümel, Sena
Deibel, Ansgar R.
Segna, Daniel
Jüngst, Christoph
Weber, Achim
Kuntzen, Thomas
Gubler, Christoph
Reiner, Cäcilia S.
description Purpose To compare the diagnostic performance of T1 mapping and MR elastography (MRE) for staging of hepatic fibrosis and grading inflammation with histopathology as standard of reference. Methods 68 patients with various liver diseases undergoing liver biopsy for suspected fibrosis or with an established diagnosis of cirrhosis prospectively underwent look-locker inversion recovery T1 mapping and MRE. T1 relaxation time and liver stiffness (LS) were measured by two readers. Hepatic fibrosis and inflammation were histopathologically staged according to a standardized fibrosis (F0–F4) and inflammation (A0–A2) score. For statistical analysis, independent t test, and Mann–Whitney U test and ROC analysis were performed, the latter to determine the performance of T1 mapping and MRE for fibrosis staging and inflammation grading, as compared to histopathology. Results Histopathological analysis diagnosed 9 patients with F0 (13.2%), 21 with F1 (30.9%), 11 with F2 (16.2%), 10 with F3 (14.7%), and 17 with F4 (25.0%). Both T1 mapping and MRE showed significantly higher values for patients with significant fibrosis (F0-1 vs. F2-4; T1 mapping p  
doi_str_mv 10.1007/s00261-022-03647-6
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Methods 68 patients with various liver diseases undergoing liver biopsy for suspected fibrosis or with an established diagnosis of cirrhosis prospectively underwent look-locker inversion recovery T1 mapping and MRE. T1 relaxation time and liver stiffness (LS) were measured by two readers. Hepatic fibrosis and inflammation were histopathologically staged according to a standardized fibrosis (F0–F4) and inflammation (A0–A2) score. For statistical analysis, independent t test, and Mann–Whitney U test and ROC analysis were performed, the latter to determine the performance of T1 mapping and MRE for fibrosis staging and inflammation grading, as compared to histopathology. Results Histopathological analysis diagnosed 9 patients with F0 (13.2%), 21 with F1 (30.9%), 11 with F2 (16.2%), 10 with F3 (14.7%), and 17 with F4 (25.0%). Both T1 mapping and MRE showed significantly higher values for patients with significant fibrosis (F0-1 vs. F2-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001) as well as for patients with severe fibrosis or cirrhosis (F0-2 vs. F3-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001). T1 values and MRE LS were significantly higher in patients with inflammation (A0 vs. A1-2, both p  = 0.01). T1 mapping showed a tendency toward lower diagnostic performance without statistical significance for significant fibrosis (F2-4) (AUC 0.79 vs. 0.91, p  = 0.06) and with a significant difference compared to MRE for severe fibrosis (F3-4) (AUC 0.79 vs. 0.94, p  = 0.03). For both T1 mapping and MRE, diagnostic performance for diagnosing hepatic inflammation (A1-2) was low (AUC 0.72 vs. 0.71, respectively). Conclusion T1 mapping is able to diagnose hepatic fibrosis, however, with a tendency toward lower diagnostic performance compared to MRE and thus may be used as an alternative to MRE for diagnosing hepatic fibrosis, whenever MRE is not available or likely to fail due to intrinsic factors of the patient. Both T1 mapping and MRE are probably not sufficient as standalone methods to diagnose hepatic inflammation with relatively low diagnostic accuracy.</description><identifier>ISSN: 2366-0058</identifier><identifier>ISSN: 2366-004X</identifier><identifier>EISSN: 2366-0058</identifier><identifier>DOI: 10.1007/s00261-022-03647-6</identifier><identifier>PMID: 36038643</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Biopsy ; Cirrhosis ; Diagnostic systems ; Elasticity Imaging Techniques - methods ; Fibrosis ; Gastroenterology ; Hepatobiliary ; Hepatology ; Histopathology ; Humans ; Imaging ; Inflammation ; Inflammation - diagnostic imaging ; Inflammation - pathology ; Liver ; Liver - diagnostic imaging ; Liver - pathology ; Liver cirrhosis ; Liver Cirrhosis - diagnostic imaging ; Liver Cirrhosis - pathology ; Liver diseases ; Magnetic resonance ; Magnetic Resonance Imaging - methods ; Mapping ; Medicine ; Medicine &amp; Public Health ; Radiology ; Reference Standards ; Relaxation time ; Statistical analysis ; Stiffness</subject><ispartof>Abdominal imaging, 2022-11, Vol.47 (11), p.3746-3757</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-3319589392a896b76c1ee50a2d2226b59087a14017f29998d7f8286e656389843</citedby><cites>FETCH-LOGICAL-c404t-3319589392a896b76c1ee50a2d2226b59087a14017f29998d7f8286e656389843</cites><orcidid>0000-0002-0902-192X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36038643$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>von Ulmenstein, Sophie</creatorcontrib><creatorcontrib>Bogdanovic, Sanja</creatorcontrib><creatorcontrib>Honcharova-Biletska, Hanna</creatorcontrib><creatorcontrib>Blümel, Sena</creatorcontrib><creatorcontrib>Deibel, Ansgar R.</creatorcontrib><creatorcontrib>Segna, Daniel</creatorcontrib><creatorcontrib>Jüngst, Christoph</creatorcontrib><creatorcontrib>Weber, Achim</creatorcontrib><creatorcontrib>Kuntzen, Thomas</creatorcontrib><creatorcontrib>Gubler, Christoph</creatorcontrib><creatorcontrib>Reiner, Cäcilia S.</creatorcontrib><title>Assessment of hepatic fibrosis and inflammation with look-locker T1 mapping and magnetic resonance elastography with histopathology as reference standard</title><title>Abdominal imaging</title><addtitle>Abdom Radiol</addtitle><addtitle>Abdom Radiol (NY)</addtitle><description>Purpose To compare the diagnostic performance of T1 mapping and MR elastography (MRE) for staging of hepatic fibrosis and grading inflammation with histopathology as standard of reference. Methods 68 patients with various liver diseases undergoing liver biopsy for suspected fibrosis or with an established diagnosis of cirrhosis prospectively underwent look-locker inversion recovery T1 mapping and MRE. T1 relaxation time and liver stiffness (LS) were measured by two readers. Hepatic fibrosis and inflammation were histopathologically staged according to a standardized fibrosis (F0–F4) and inflammation (A0–A2) score. For statistical analysis, independent t test, and Mann–Whitney U test and ROC analysis were performed, the latter to determine the performance of T1 mapping and MRE for fibrosis staging and inflammation grading, as compared to histopathology. Results Histopathological analysis diagnosed 9 patients with F0 (13.2%), 21 with F1 (30.9%), 11 with F2 (16.2%), 10 with F3 (14.7%), and 17 with F4 (25.0%). Both T1 mapping and MRE showed significantly higher values for patients with significant fibrosis (F0-1 vs. F2-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001) as well as for patients with severe fibrosis or cirrhosis (F0-2 vs. F3-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001). T1 values and MRE LS were significantly higher in patients with inflammation (A0 vs. A1-2, both p  = 0.01). T1 mapping showed a tendency toward lower diagnostic performance without statistical significance for significant fibrosis (F2-4) (AUC 0.79 vs. 0.91, p  = 0.06) and with a significant difference compared to MRE for severe fibrosis (F3-4) (AUC 0.79 vs. 0.94, p  = 0.03). For both T1 mapping and MRE, diagnostic performance for diagnosing hepatic inflammation (A1-2) was low (AUC 0.72 vs. 0.71, respectively). Conclusion T1 mapping is able to diagnose hepatic fibrosis, however, with a tendency toward lower diagnostic performance compared to MRE and thus may be used as an alternative to MRE for diagnosing hepatic fibrosis, whenever MRE is not available or likely to fail due to intrinsic factors of the patient. Both T1 mapping and MRE are probably not sufficient as standalone methods to diagnose hepatic inflammation with relatively low diagnostic accuracy.</description><subject>Biopsy</subject><subject>Cirrhosis</subject><subject>Diagnostic systems</subject><subject>Elasticity Imaging Techniques - methods</subject><subject>Fibrosis</subject><subject>Gastroenterology</subject><subject>Hepatobiliary</subject><subject>Hepatology</subject><subject>Histopathology</subject><subject>Humans</subject><subject>Imaging</subject><subject>Inflammation</subject><subject>Inflammation - diagnostic imaging</subject><subject>Inflammation - pathology</subject><subject>Liver</subject><subject>Liver - diagnostic imaging</subject><subject>Liver - pathology</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - diagnostic imaging</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver diseases</subject><subject>Magnetic resonance</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mapping</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Radiology</subject><subject>Reference Standards</subject><subject>Relaxation time</subject><subject>Statistical analysis</subject><subject>Stiffness</subject><issn>2366-0058</issn><issn>2366-004X</issn><issn>2366-0058</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxiMEolXpC3BAlrhwCYztxLEvSFUFLVIlLuVsebOTxG1iB0-Wah-Ft8XblFI4cPLI85tv_nxF8ZrDew7QfCAAoXgJQpQgVdWU6llxLKRSJUCtnz-Jj4pTohsA4KrmXNQviyOpQGpVyePi5xkREk0YFhY7NuDsFt-yzm9SJE_MhS3zoRvdNOVEDOzOLwMbY7wtx9jeYmLXnE1unn3o7-HJ9QEPEgkpBhdaZDg6WmKf3Dzs1_rB54_caYhj7PfMUaY7THigackyLm1fFS86NxKePrwnxbfPn67PL8urrxdfzs-uyraCaiml5KbWRhrhtFGbRrUcsQYntkIItakN6MbxCnjTCWOM3jadFlqhqpXURlfypPi46s67zYTbNl8iudHOyU8u7W103v6dCX6wffxhTa3AVDwLvHsQSPH7Dmmxk6cWx9EFjDuyogEtap0nzOjbf9CbuEshr5cpUVW8afhhIrFSbfaA8mUeh-FgD-bb1Xybzbf35luVi948XeOx5LfVGZArQDkVekx_ev9H9hdI5rx-</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>von Ulmenstein, Sophie</creator><creator>Bogdanovic, Sanja</creator><creator>Honcharova-Biletska, Hanna</creator><creator>Blümel, Sena</creator><creator>Deibel, Ansgar R.</creator><creator>Segna, Daniel</creator><creator>Jüngst, Christoph</creator><creator>Weber, Achim</creator><creator>Kuntzen, Thomas</creator><creator>Gubler, Christoph</creator><creator>Reiner, Cäcilia S.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0902-192X</orcidid></search><sort><creationdate>20221101</creationdate><title>Assessment of hepatic fibrosis and inflammation with look-locker T1 mapping and magnetic resonance elastography with histopathology as reference standard</title><author>von Ulmenstein, Sophie ; Bogdanovic, Sanja ; Honcharova-Biletska, Hanna ; Blümel, Sena ; Deibel, Ansgar R. ; Segna, Daniel ; Jüngst, Christoph ; Weber, Achim ; Kuntzen, Thomas ; Gubler, Christoph ; Reiner, Cäcilia S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-3319589392a896b76c1ee50a2d2226b59087a14017f29998d7f8286e656389843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biopsy</topic><topic>Cirrhosis</topic><topic>Diagnostic systems</topic><topic>Elasticity Imaging Techniques - methods</topic><topic>Fibrosis</topic><topic>Gastroenterology</topic><topic>Hepatobiliary</topic><topic>Hepatology</topic><topic>Histopathology</topic><topic>Humans</topic><topic>Imaging</topic><topic>Inflammation</topic><topic>Inflammation - diagnostic imaging</topic><topic>Inflammation - pathology</topic><topic>Liver</topic><topic>Liver - diagnostic imaging</topic><topic>Liver - pathology</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - diagnostic imaging</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver diseases</topic><topic>Magnetic resonance</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mapping</topic><topic>Medicine</topic><topic>Medicine &amp; 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Methods 68 patients with various liver diseases undergoing liver biopsy for suspected fibrosis or with an established diagnosis of cirrhosis prospectively underwent look-locker inversion recovery T1 mapping and MRE. T1 relaxation time and liver stiffness (LS) were measured by two readers. Hepatic fibrosis and inflammation were histopathologically staged according to a standardized fibrosis (F0–F4) and inflammation (A0–A2) score. For statistical analysis, independent t test, and Mann–Whitney U test and ROC analysis were performed, the latter to determine the performance of T1 mapping and MRE for fibrosis staging and inflammation grading, as compared to histopathology. Results Histopathological analysis diagnosed 9 patients with F0 (13.2%), 21 with F1 (30.9%), 11 with F2 (16.2%), 10 with F3 (14.7%), and 17 with F4 (25.0%). Both T1 mapping and MRE showed significantly higher values for patients with significant fibrosis (F0-1 vs. F2-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001) as well as for patients with severe fibrosis or cirrhosis (F0-2 vs. F3-4; T1 mapping p  &lt; 0.0001, MRE p  &lt; 0.0001). T1 values and MRE LS were significantly higher in patients with inflammation (A0 vs. A1-2, both p  = 0.01). T1 mapping showed a tendency toward lower diagnostic performance without statistical significance for significant fibrosis (F2-4) (AUC 0.79 vs. 0.91, p  = 0.06) and with a significant difference compared to MRE for severe fibrosis (F3-4) (AUC 0.79 vs. 0.94, p  = 0.03). For both T1 mapping and MRE, diagnostic performance for diagnosing hepatic inflammation (A1-2) was low (AUC 0.72 vs. 0.71, respectively). Conclusion T1 mapping is able to diagnose hepatic fibrosis, however, with a tendency toward lower diagnostic performance compared to MRE and thus may be used as an alternative to MRE for diagnosing hepatic fibrosis, whenever MRE is not available or likely to fail due to intrinsic factors of the patient. Both T1 mapping and MRE are probably not sufficient as standalone methods to diagnose hepatic inflammation with relatively low diagnostic accuracy.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36038643</pmid><doi>10.1007/s00261-022-03647-6</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0902-192X</orcidid><oa>free_for_read</oa></addata></record>
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source Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List
subjects Biopsy
Cirrhosis
Diagnostic systems
Elasticity Imaging Techniques - methods
Fibrosis
Gastroenterology
Hepatobiliary
Hepatology
Histopathology
Humans
Imaging
Inflammation
Inflammation - diagnostic imaging
Inflammation - pathology
Liver
Liver - diagnostic imaging
Liver - pathology
Liver cirrhosis
Liver Cirrhosis - diagnostic imaging
Liver Cirrhosis - pathology
Liver diseases
Magnetic resonance
Magnetic Resonance Imaging - methods
Mapping
Medicine
Medicine & Public Health
Radiology
Reference Standards
Relaxation time
Statistical analysis
Stiffness
title Assessment of hepatic fibrosis and inflammation with look-locker T1 mapping and magnetic resonance elastography with histopathology as reference standard
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