Evidence map›Paper›PMID 41244053›Full record

ArticleFrontiers in endocrinology2025

Explainable machine learning model for classifying atherosclerotic cardiovascular disease in patients with metabolic dysfunction-associated steatotic liver disease.

Zhengliang Li, Xiaokai Chen, Linlin Ren, Banghui Wang, Shimiao Ruan, Juan Wang, Wenzhong Zhang

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Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhengliang Li *Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xiaokai Chen *Department of Gastroenterology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Linlin RenDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Banghui WangDepartment of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Shimiao RuanDepartment of Emergency, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Juan WangDepartment of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Wenzhong ZhangDepartment of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cardiovascular disease (CVD) is the leading cause of mortality in patients with metabolic dysfunction-associated steatotic liver disease (MASLD), yet traditional risk predictors remain limited in clinical practice. Objective: To develop machine learning (ML) models for classifying prevalent atherosclerotic cardiovascular disease (ASCVD) risk in MASLD patients, and to enhance model interpretability using SHapley Additive exPlanations (SHAP). Methods: This retrospective study included 590 MASLD patients diagnosed at the Affiliated Hospital of Qingdao University between December 2019 and December 2024. Patients were randomly divided into a training set (n=413) and a validation set (n=177), and further stratified based on ASCVD status. Least absolute shrinkage and selection operator (LASSO) regression was used for feature selection. Six ML models were developed and evaluated using sensitivity, specificity, accuracy, area under the receiver operating characteristic curve (AUC), and F1 score. SHAP analysis was performed to interpret feature contributions. Results: ASCVD was present in 434 of 590 patients (73.6%). The Gradient Boosting (GB) model achieved the best performance, with AUCs of 0.918 (95% CI: 0.890-0.944) in the training set and 0.817 (95% CI: 0.739-0.883) in the validation set. SHAP analysis identified the top predictors as the Cholesterol-HDL-Glucose (CHG) index, Castelli Risk Index II (CRI-II), lipoprotein(a) [Lp(a)], serum creatinine (Scr), and uric acid (UA). Conclusion: The GB model demonstrated strong high accuracy in identifying existing ASCVD in MASLD patients and may serve as a useful tool for early risk stratification in clinical settings.

Indexed as

AtherosclerosisCardiovascular DiseasesFatty LiverMachine LearningAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsROC Curveatherosclerotic cardiovascular diseasecomposite metabolic indexmachine learningmetabolic dysfunction-associated steatotic liver diseaseSHAP interpretability model

Identifiers

PMID41244053
PMCPMC12611696

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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.