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Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center

Low cut-off of FIB-4 is a widely used formula to exclude advanced liver fibrosis in primary care centers. However, the range of reported threshold of FIB-4 to rule in advanced fibrosis is too broad across etiologies, and no consensus has been reached. In the present study, we investigated the role o...

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Autores principales: Roh, Yun Hwa, Kang, Bo-Kyeong, Jun, Dae Won, Lee, Chul-min, Kim, Mimi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245508/
https://www.ncbi.nlm.nih.gov/pubmed/34193951
http://dx.doi.org/10.1038/s41598-021-93038-6
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author Roh, Yun Hwa
Kang, Bo-Kyeong
Jun, Dae Won
Lee, Chul-min
Kim, Mimi
author_facet Roh, Yun Hwa
Kang, Bo-Kyeong
Jun, Dae Won
Lee, Chul-min
Kim, Mimi
author_sort Roh, Yun Hwa
collection PubMed
description Low cut-off of FIB-4 is a widely used formula to exclude advanced liver fibrosis in primary care centers. However, the range of reported threshold of FIB-4 to rule in advanced fibrosis is too broad across etiologies, and no consensus has been reached. In the present study, we investigated the role of FIB-4 for a reassessment of hepatic fibrosis burden in a referral center. We compared the diagnostic performance of FIB-4 among patients with liver disease of various causes and tried to find an optimal cut-off value for predicting advanced fibrosis. Among 1068 patients, the AUROC of FIB-4 to diagnose advanced fibrosis showed no significant difference among the various etiologies of liver disease, ranging from 0.783 to 0.821. The optimal cut-off value obtained by maximizing Youden's index was 2.68, and the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for predicting advanced fibrosis were 70.7%, 79.1%, 43.5%, and 92.2%, respectively. The PPV was low in patients with autoimmune disease (6.67%). When we incorporated the new cut-off of FIB-4 into abdominal ultrasound findings, 81% of unnecessary work-ups would be appropriately avoided. In conclusion, the cut-off value of 2.68 showed an acceptable PPV while maintaining a high NPV to predict advanced fibrosis, most etiology except for autoimmune diseases. This result could assist in establishing an appropriate timing to reassess the hepatic fibrosis burden during monitoring in the referral center.
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spelling pubmed-82455082021-07-06 Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center Roh, Yun Hwa Kang, Bo-Kyeong Jun, Dae Won Lee, Chul-min Kim, Mimi Sci Rep Article Low cut-off of FIB-4 is a widely used formula to exclude advanced liver fibrosis in primary care centers. However, the range of reported threshold of FIB-4 to rule in advanced fibrosis is too broad across etiologies, and no consensus has been reached. In the present study, we investigated the role of FIB-4 for a reassessment of hepatic fibrosis burden in a referral center. We compared the diagnostic performance of FIB-4 among patients with liver disease of various causes and tried to find an optimal cut-off value for predicting advanced fibrosis. Among 1068 patients, the AUROC of FIB-4 to diagnose advanced fibrosis showed no significant difference among the various etiologies of liver disease, ranging from 0.783 to 0.821. The optimal cut-off value obtained by maximizing Youden's index was 2.68, and the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for predicting advanced fibrosis were 70.7%, 79.1%, 43.5%, and 92.2%, respectively. The PPV was low in patients with autoimmune disease (6.67%). When we incorporated the new cut-off of FIB-4 into abdominal ultrasound findings, 81% of unnecessary work-ups would be appropriately avoided. In conclusion, the cut-off value of 2.68 showed an acceptable PPV while maintaining a high NPV to predict advanced fibrosis, most etiology except for autoimmune diseases. This result could assist in establishing an appropriate timing to reassess the hepatic fibrosis burden during monitoring in the referral center. Nature Publishing Group UK 2021-06-30 /pmc/articles/PMC8245508/ /pubmed/34193951 http://dx.doi.org/10.1038/s41598-021-93038-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Roh, Yun Hwa
Kang, Bo-Kyeong
Jun, Dae Won
Lee, Chul-min
Kim, Mimi
Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title_full Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title_fullStr Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title_full_unstemmed Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title_short Role of FIB-4 for reassessment of hepatic fibrosis burden in referral center
title_sort role of fib-4 for reassessment of hepatic fibrosis burden in referral center
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245508/
https://www.ncbi.nlm.nih.gov/pubmed/34193951
http://dx.doi.org/10.1038/s41598-021-93038-6
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