Diagnostic accuracy of non-invasive tests for advanced fibrosis in patients with NAFLD: an individual patient data meta-analysis.
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BORIS DOI
Date of Publication
May 2022
Publication Type
Article
Division/Institute
Author
Mózes, Ferenc Emil | |
Lee, Jenny A | |
Selvaraj, Emmanuel Anandraj | |
Jayaswal, Arjun Narayan Ajmer | |
Trauner, Michael | |
Boursier, Jerome | |
Fournier, Céline | |
Stauber, Rudolf E | |
Bugianesi, Elisabetta | |
Younes, Ramy | |
Gaia, Silvia | |
Lupșor-Platon, Monica | |
Petta, Salvatore | |
Shima, Toshihide | |
Okanoue, Takeshi | |
Mahadeva, Sanjiv | |
Chan, Wah-Kheong | |
Eddowes, Peter J | |
Hirschfield, Gideon M | |
Newsome, Philip Noel | |
Wong, Vincent Wai-Sun | |
de Ledinghen, Victor | |
Fan, Jiangao | |
Shen, Feng | |
Cobbold, Jeremy F | |
Sumida, Yoshio | |
Okajima, Akira | |
Schattenberg, Jörn M | |
Labenz, Christian | |
Kim, Won | |
Lee, Myoung Seok | |
Wiegand, Johannes | |
Karlas, Thomas | |
Yılmaz, Yusuf | |
Aithal, Guruprasad Padur | |
Palaniyappan, Naaventhan | |
Cassinotto, Christophe | |
Aggarwal, Sandeep | |
Garg, Harshit | |
Ooi, Geraldine J | |
Nakajima, Atsushi | |
Yoneda, Masato | |
Ziol, Marianne | |
Barget, Nathalie | |
Geier, Andreas | |
Tuthill, Theresa | |
Brosnan, M Julia | |
Anstee, Quentin Mark | |
Neubauer, Stefan | |
Harrison, Stephen A | |
Bossuyt, Patrick M | |
Pavlides, Michael |
Subject(s)
Series
Gut
ISSN or ISBN (if monograph)
0017-5749
Publisher
BMJ Publishing Group
Language
English
Publisher DOI
PubMed ID
34001645
Uncontrolled Keywords
Description
OBJECTIVE
Liver biopsy is still needed for fibrosis staging in many patients with non-alcoholic fatty liver disease. The aims of this study were to evaluate the individual diagnostic performance of liver stiffness measurement by vibration controlled transient elastography (LSM-VCTE), Fibrosis-4 Index (FIB-4) and NAFLD (non-alcoholic fatty liver disease) Fibrosis Score (NFS) and to derive diagnostic strategies that could reduce the need for liver biopsies.
DESIGN
Individual patient data meta-analysis of studies evaluating LSM-VCTE against liver histology was conducted. FIB-4 and NFS were computed where possible. Sensitivity, specificity and area under the receiver operating curve (AUROC) were calculated. Biomarkers were assessed individually and in sequential combinations.
RESULTS
Data were included from 37 primary studies (n=5735; 45% women; median age: 54 years; median body mass index: 30 kg/m2; 33% had type 2 diabetes; 30% had advanced fibrosis). AUROCs of individual LSM-VCTE, FIB-4 and NFS for advanced fibrosis were 0.85, 0.76 and 0.73. Sequential combination of FIB-4 cut-offs (<1.3; ≥2.67) followed by LSM-VCTE cut-offs (<8.0; ≥10.0 kPa) to rule-in or rule-out advanced fibrosis had sensitivity and specificity (95% CI) of 66% (63-68) and 86% (84-87) with 33% needing a biopsy to establish a final diagnosis. FIB-4 cut-offs (<1.3; ≥3.48) followed by LSM cut-offs (<8.0; ≥20.0 kPa) to rule out advanced fibrosis or rule in cirrhosis had a sensitivity of 38% (37-39) and specificity of 90% (89-91) with 19% needing biopsy.
CONCLUSION
Sequential combinations of markers with a lower cut-off to rule-out advanced fibrosis and a higher cut-off to rule-in cirrhosis can reduce the need for liver biopsies.
Liver biopsy is still needed for fibrosis staging in many patients with non-alcoholic fatty liver disease. The aims of this study were to evaluate the individual diagnostic performance of liver stiffness measurement by vibration controlled transient elastography (LSM-VCTE), Fibrosis-4 Index (FIB-4) and NAFLD (non-alcoholic fatty liver disease) Fibrosis Score (NFS) and to derive diagnostic strategies that could reduce the need for liver biopsies.
DESIGN
Individual patient data meta-analysis of studies evaluating LSM-VCTE against liver histology was conducted. FIB-4 and NFS were computed where possible. Sensitivity, specificity and area under the receiver operating curve (AUROC) were calculated. Biomarkers were assessed individually and in sequential combinations.
RESULTS
Data were included from 37 primary studies (n=5735; 45% women; median age: 54 years; median body mass index: 30 kg/m2; 33% had type 2 diabetes; 30% had advanced fibrosis). AUROCs of individual LSM-VCTE, FIB-4 and NFS for advanced fibrosis were 0.85, 0.76 and 0.73. Sequential combination of FIB-4 cut-offs (<1.3; ≥2.67) followed by LSM-VCTE cut-offs (<8.0; ≥10.0 kPa) to rule-in or rule-out advanced fibrosis had sensitivity and specificity (95% CI) of 66% (63-68) and 86% (84-87) with 33% needing a biopsy to establish a final diagnosis. FIB-4 cut-offs (<1.3; ≥3.48) followed by LSM cut-offs (<8.0; ≥20.0 kPa) to rule out advanced fibrosis or rule in cirrhosis had a sensitivity of 38% (37-39) and specificity of 90% (89-91) with 19% needing biopsy.
CONCLUSION
Sequential combinations of markers with a lower cut-off to rule-out advanced fibrosis and a higher cut-off to rule-in cirrhosis can reduce the need for liver biopsies.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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gutjnl-2021-324243.full.pdf | text | Adobe PDF | 1.54 MB | published |