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Article: LiveBoost: A GB-based prediction system for liver fibrosis in chronic hepatitis B patients in China - A multi-center retrospective study

TitleLiveBoost: A GB-based prediction system for liver fibrosis in chronic hepatitis B patients in China - A multi-center retrospective study
Authors
KeywordsAPRI
Chronic hepatitis B
FIB-4
Hepatic fibrosis
LiveBoost
Issue Date30-Jan-2024
PublisherElsevier
Citation
Heliyon, 2024, v. 10, n. 2 How to Cite?
AbstractBackground: The aim of this study was to evaluate the accuracy of LiveBoostâ„¢, a gradient boosting (GB)-based prediction system based on standard biochemical values (AST, ALT, platelet count) and age, in Chinese patients with chronic hepatitis B (CHB) and compare its performance with FIB-4 (fibrosis-4 score) and APRI (the aspartate transaminase to platelet ratio index). Methods: This retrospective trial enrolled 454 participants, including 279 CHB patients who underwent liver biopsy and 175 normal controls from 3 centers in China. All participants underwent laboratory blood testing. LiveBoost was constructed using GB and FIB-4 and APRI were calculated from laboratory data. Results: LiveBoost outperformed APRI and FIB-4 in predicting hepatic fibrosis and cirrhosis. The GB model had an AUROC of 0.977 for CHB diagnosis, 0.804 for early and advanced fibrosis, and 0.836 for non-cirrhosis and cirrhosis, compared to AUROC of 0.554, 0.673 and 0.720 for FIB-4, AUROC of 0.977, 0.652 and 0.654 for APRI. Conclusions: LiveBoost is a more reliable and cost-effective method than APRI and FIB-4 for assessing liver fibrosis in Chinese patients with CHB.
Persistent Identifierhttp://hdl.handle.net/10722/348404

 

DC FieldValueLanguage
dc.contributor.authorXie, Guoxiang-
dc.contributor.authorXiao, Huanming-
dc.contributor.authorLiu, Quan-
dc.contributor.authorChen, Tianlu-
dc.contributor.authorChen, Fengyan-
dc.contributor.authorZhou, Kejun-
dc.contributor.authorWang, Xiaoning-
dc.contributor.authorLiu, Ping-
dc.contributor.authorJia, Zhifeng-
dc.contributor.authorChen, Lei-
dc.contributor.authorDeng, Xin-
dc.contributor.authorMeng, Fankun-
dc.contributor.authorZhang, Zhenhua-
dc.contributor.authorChi, Xiaoling-
dc.contributor.authorJia, Wei-
dc.date.accessioned2024-10-09T00:31:18Z-
dc.date.available2024-10-09T00:31:18Z-
dc.date.issued2024-01-30-
dc.identifier.citationHeliyon, 2024, v. 10, n. 2-
dc.identifier.urihttp://hdl.handle.net/10722/348404-
dc.description.abstractBackground: The aim of this study was to evaluate the accuracy of LiveBoostâ„¢, a gradient boosting (GB)-based prediction system based on standard biochemical values (AST, ALT, platelet count) and age, in Chinese patients with chronic hepatitis B (CHB) and compare its performance with FIB-4 (fibrosis-4 score) and APRI (the aspartate transaminase to platelet ratio index). Methods: This retrospective trial enrolled 454 participants, including 279 CHB patients who underwent liver biopsy and 175 normal controls from 3 centers in China. All participants underwent laboratory blood testing. LiveBoost was constructed using GB and FIB-4 and APRI were calculated from laboratory data. Results: LiveBoost outperformed APRI and FIB-4 in predicting hepatic fibrosis and cirrhosis. The GB model had an AUROC of 0.977 for CHB diagnosis, 0.804 for early and advanced fibrosis, and 0.836 for non-cirrhosis and cirrhosis, compared to AUROC of 0.554, 0.673 and 0.720 for FIB-4, AUROC of 0.977, 0.652 and 0.654 for APRI. Conclusions: LiveBoost is a more reliable and cost-effective method than APRI and FIB-4 for assessing liver fibrosis in Chinese patients with CHB.-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofHeliyon-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAPRI-
dc.subjectChronic hepatitis B-
dc.subjectFIB-4-
dc.subjectHepatic fibrosis-
dc.subjectLiveBoost-
dc.titleLiveBoost: A GB-based prediction system for liver fibrosis in chronic hepatitis B patients in China - A multi-center retrospective study-
dc.typeArticle-
dc.identifier.doi10.1016/j.heliyon.2024.e24161-
dc.identifier.scopuseid_2-s2.0-85182010709-
dc.identifier.volume10-
dc.identifier.issue2-
dc.identifier.eissn2405-8440-
dc.identifier.issnl2405-8440-

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