Evidence map›Paper›PMID 40050685›Full record

ArticleScientific reports2025

An interpretable machine learning-assisted diagnostic model for Kawasaki disease in children.

Mengyu Duan, Zhimin Geng, Lichao Gao, Yonggen Zhao, Zheming Li, Lindong Chen, Pekka Kuosmanen, Guoqiang Qi, Fangqi Gong, Gang Yu

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Mengyu Duan *National Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhimin Geng *National Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Lichao GaoNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yonggen ZhaoNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zheming LiNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Lindong ChenNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Pekka KuosmanenSino-Finland Joint AI Laboratory for Child Health of Zhejiang Province, Hangzhou, China.
Guoqiang QiNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China. qiguoqiang@zju.edu.cn.
Fangqi GongNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China. gongfangqi@zju.edu.cn.
Gang YuNational Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China. yugbme@zju.edu.cn.

Funding

Key R&D Program of Zhejiang 2024C03180National Key Research and Development Program of China 2023YFC2706400
6 · The paper itself

Abstract

Kawasaki disease (KD) is a syndrome of acute systemic vasculitis commonly observed in children. Due to its unclear pathogenesis and the lack of specific diagnostic markers, it is prone to being confused with other diseases that exhibit similar symptoms, making early and accurate diagnosis challenging. This study aimed to develop an interpretable machine learning (ML) diagnostic model for KD. We collected demographic and laboratory data from 3650 patients (2299 with KD, 1351 with similar symptoms but different diseases) and employed 10 ML algorithms to construct the diagnostic model. Diagnostic performance was evaluated using several metrics, including area under the receiver-operating characteristic curve (AUC). Additionally, the shapley additive explanations (SHAP) method was employed to select important features and explain the final model. Using the Streamlit framework, we converted the model into a user-friendly web application to enhance its practicality in clinical settings. Among the 10 ML algorithms, XGBoost demonstrates the best diagnostic performance, achieving an AUC of 0.9833. SHAP analysis revealed that features, including age in months, fibrinogen, and human interferon gamma, are important for diagnosis. When relying on the top 10 most important features, the model's AUC remains at 0.9757. The proposed model can assist clinicians in making early and accurate diagnoses of KD. Furthermore, its interpretability enhances model transparency, facilitating clinicians' understanding of prediction reliability.

Indexed as

Machine LearningMucocutaneous Lymph Node SyndromeAlgorithmsArea Under CurveChildChild, PreschoolFemaleHumansInfantMaleROC CurveInterpretabilityKawasaki diseaseMachine learningSHAPStreamlit.XGBoost

Identifiers

PMID40050685
PMCPMC11885592

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Registered trials

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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.