Evidence mapPaperPMID 42267251Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2026

Incorporating Insulin Resistance Biomarkers into Machine Learning Models Enhances Diagnostic Accuracy for Metabolic Dysfunction-Associated Steatotic Liver Disease.

Jingyuan Nie, Jing Zhou, Yuanjia Hu, Changhong Zhang, Pingping Yu, Xun Lei

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Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 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

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5 · Who and what money

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6 authors.

Jingyuan Nie *Department of Epidemiology and Health Statistics, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Jing Zhou *Department of Epidemiology and Health Statistics, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.ORCID 0009-0005-7122-1104
Yuanjia HuDepartment of Epidemiology and Health Statistics, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Changhong ZhangDepartment of Epidemiology and Health Statistics, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Pingping YuHealth Medical Center, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, People's Republic of China.
Xun LeiDepartment of Epidemiology and Health Statistics, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.ORCID 0009-0007-6211-4029

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as the most prevalent chronic liver disorder worldwide. Despite its increasing prevalence, MASLD is often asymptomatic in its early course, leading to considerable underdiagnosis. Insulin resistance (IR) plays a key role in MASLD development; however, the incremental value of IR-related biomarkers in machine learning (ML) diagnostic models for MASLD has not been fully investigated. Methods: This retrospective single-center study included 18,535 adults (5992 with MASLD and 12,543 without MASLD) undergoing routine health examinations at our research center. Two feature sets were created: Set 1 included demographic, anthropometric, clinical, and biochemical indicators, while Set 2 further incorporated IR-related biomarkers, including triglyceride-glucose (TyG)-based indices and the metabolic score for insulin resistance (METS-IR). Six ML algorithms were used to develop diagnostic models. Model performance was assessed using sensitivity, specificity, F1-score, and area under the curve (AUC) on the training and validation sets, with clinical utility evaluated using decision curve analysis (DCA). Model interpretability was further explored using Shapley Additive exPlanations (SHAP). Results: All six ML models demonstrated a statistically significant improvement in AUC values after incorporating IR-related biomarkers (all P < 0.05). In the validation set, the extremely randomized trees (ERT) model with Set 2 achieved the highest AUC (0.901). DCA further indicated that models incorporating IR-related biomarkers generally provided a higher net clinical benefit. Overall, the ERT model provided the most favorable combination of discrimination and clinical utility. SHAP analysis further emphasized the important role of IR-related biomarkers in MASLD diagnosis. Conclusion: Incorporating IR-related biomarkers into ML diagnostic models improved the accuracy and clinical utility of MASLD detection without increasing testing costs or patient burden. These findings highlight the incremental diagnostic value of IR-related biomarkers in ML models and support their use as a decision-support tool for MASLD screening in general populations.

Indexed as

diagnostic modelinsulin resistancemachine learningmetabolic dysfunction-associated steatotic liver disease

Identifiers

PMID42267251
PMCPMC13245621

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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 Socratic graph.