Evidence map›Paper›PMID 42044931›Full record

ArticleLupus science & medicine2026

Validity and applicability of machine learning models for systemic lupus erythematosus diagnosis.

Rui-Cen Li, An-Fang Huang, Lin-Chong Su, Da-Cheng Wang, Wang-Dong Xu

Abstract readValidation Study
In one paragraph

Article in Lupus science & medicine, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Rui-Cen LiHealth Management Center, West China Hospital, Chengdu, Sichuan, China.
An-Fang HuangDepartment of Rheumatology and Immunology, The Affiliated Hospital, Luzhou, Sichuan, China.ORCID 0000-0002-3860-8383
Lin-Chong SuHubei Provincial Key Laboratory of Occurrence and Intervention of Rheumatic Diseases, Affiliated Minda Hospital of Hubei Minzu University, Enshi, Hubei, China.
Da-Cheng WangDepartment of Evidence-Based Medicine, Southwest Medical University, Luzhou, Sichuan, China loutch123@163.com 1310781487@qq.com.
Wang-Dong XuSouthwest Medical University, Luzhou, Sichuan, China loutch123@163.com 1310781487@qq.com.ORCID 0000-0001-8276-1249

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of systemic lupus erythematosus (SLE) is clinically complex, and early identification is essential for timely intervention and reducing disease burden. Machine learning offers a promising approach to distinguish early-stage SLE patients from healthy individuals.

methodsA total of 2672 SLE patients and 154 798 healthy controls from the Luzhou (discovery) cohort, along with 2532 SLE patients and 38 597 healthy controls from the Enshi (validation) cohort, were enrolled in this study. A complete machine learning pipeline-including data preprocessing, feature selection, model training and postanalysis, was developed in the Luzhou cohort and subsequently validated in the Enshi cohort. Optimal features and the best-performing model were identified in the Luzhou cohort, then scaled and validated in the Enshi cohort. Model performance was evaluated using 13 binary classification metrics. The optimal feature set and model were integrated to construct an Artificial Intelligence Prediction tool for SLE (AI-PSLE).

resultsFifty candidate features were initially selected in the Luzhou cohort, among which the light gradient boosting (LGB) model demonstrated the best performance following data preprocessing. After scaling in the Enshi cohort, 35 reproducible features were retained. The LGB model based on these 35 features maintained superior performance in the Luzhou cohort and was further successfully validated in both the Enshi and combined Luzhou+Enshi cohorts.

conclusionsWe developed an open-access, clinically user-friendly tool-AI-PSLE-based on 35 routine features, aimed at facilitating the early identification of SLE patients from healthy populations.

Indexed as

Lupus Erythematosus, SystemicMachine LearningAdultBoosting Machine Learning AlgorithmsCase-Control StudiesClassification AlgorithmsCohort StudiesFemaleHumansMaleMiddle AgedPredictive Learning ModelsReproducibility of ResultsAutoimmunityLupus Erythematosus, SystemicRisk Factors

Identifiers

PMID42044931
PMCPMC13141063

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