Evidence map›Paper›PMID 42436479›Full record

ArticleBMC medical informatics and decision making2026

Development and validation of a machine learning model for identifying liver fibrosis in MAFLD: a retrospective model development study.

Chenyu Hu, Yu Qiu, Yuxin Zhong, Wei Zhou, Zhiqi Zhang, Yi Huang

Abstract readValidation Study
In one paragraph

Article in BMC medical informatics and decision making, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chenyu Hu *Department of Hepatic Diseases, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.
Yu Qiu *Department of Hepatic Diseases, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.
Yuxin ZhongClinical Medical College, Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China.
Wei ZhouDepartment of Hepatic Diseases, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.
Zhiqi ZhangDepartment of Hepatic Diseases, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.
Yi HuangDepartment of Hepatic Diseases, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China. hy11_22@sina.com.

Funding

Chongqing Hospital of Traditional Chinese Medicine CQEIC2024MDAD-042
6 · The paper itself

Abstract

backgroundMetabolic dysfunction-associated fatty liver disease (MAFLD), as the most prevalent chronic liver disease globally, is closely related to the prevalence of metabolic syndrome. Liver fibrosis is a core stage in the progression of this disease, significantly increasing the risk of liver cirrhosis, liver failure, and hepatocellular carcinoma. Early identification of high-risk patients is crucial for blocking disease progression. We developed and internally validated a machine learning model to identify MAFLD patients with VCTE-defined liver fibrosis using routinely collected clinical variables.

methodThis study selected 2728 research subjects from January 2020 to October 2025. Through the least absolute shrinkage and selection operator (LASSO) regression, Boruta algorithm, and recursive feature elimination (RFE), eight key variables, namely ALT, AST, SBP, BMI, WHR, DBP, LDL-C, and GGT, were selected. Classification models employed logistic regression, decision trees, random forests, XGBoost, LightGBM, support vector machines (SVM), and artificial neural networks (ANN). Nomogram and SHapley additive exPlanations (SHAP) were used to explain the constructed model.

resultsThis study included 2728 patients with 1013 cases (38%) of liver fibrosis. XGBoost, LightGBM, and Random Forest demonstrated broadly comparable performance.

conclusionThe proposed machine learning model has clinical application potential in identifying liver fibrosis defined by VCTE in patients with MAFLD. External validation and prospective clinical evaluation are required before routine clinical implementation.

Indexed as

Liver CirrhosisMachine LearningNon-alcoholic Fatty Liver DiseaseBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansMaleMiddle AgedPredictive Learning ModelsRandom ForestRetrospective StudiesArtificial intelligenceExplainable AILiver fibrosisMachine learningMetabolic dysfunction-associated fatty liver disease (MAFLD)

Identifiers

PMID42436479
PMCPMC13640069

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.