Evidence map›Paper›PMID 41884119›Full record

ArticleJournal of translational autoimmunity2026

Machine learning for predicting macrophage activation syndrome in adult patients with Still's disease.

Yihe Zheng, Changyi Yang, Xiaoxuan Cai, Jie Zhao, Zile Chen, Shuni Ying, Jianjun Qiao

Abstract read
In one paragraph

Article in Journal of translational autoimmunity, 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yihe ZhengDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Changyi YangDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaoxuan CaiDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jie ZhaoDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zile ChenDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shuni YingDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jianjun QiaoDepartment of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Macrophage activation syndrome (MAS) secondary to Still's disease is a potentially fatal complication, associated with mortality rates exceeding 10%. Early identification is critical for survival but remains challenging due to the lack of specific predictive biomarkers. Objective: To develop and test an explainable model to predict MAS in adult patients with Still's disease using routine baseline clinical parameters, and to implement it as an interactive tool. Methods: We conducted a retrospective model development and testing study across four hospital sites from Aug 1, 2019 to Jul 31, 2025. Adults meeting the Yamaguchi criteria for Still's disease were included. Demographics, imaging/physical findings, and routine laboratory tests within 48 h of admission were analyzed. Predictors were selected using nested cross-validated LASSO, and five algorithms (logistic regression, random forest, SVM, XGBoost, and LightGBM) were compared. Model interpretability was assessed with SHAP, and a bedside score was derived using Firth's penalized logistic regression. Results: A total of 312 patients with Still's disease was included, with model development in two centers (n = 226) and testing in two independent centers (n = 86). The final XGBoost model retained five key predictors: ferritin, splenomegaly, platelet count, total cholesterol, and erythrocyte sedimentation rate, achieving an AUC of 0.839 in the test set, with a sensitivity of 0.824, specificity of 0.710, acceptable calibration (Brier 0.136), and favorable net clinical benefit. The derived 0-10 bedside risk score stratified the training cohort into low- (1%), intermediate- (14.6%), and high-risk (75%) MAS groups. Conclusions: We present an interpretable machine learning model based on baseline data and simplified risk score for predicting in-hospital MAS in adult patients with Still's disease. To our knowledge, this study represents one of the larger adult cohorts assembled for Still's disease-associated MAS.

Indexed as

Machine learningMacrophage activation syndromeStill's disease

Identifiers

PMID41884119
PMCPMC13010447

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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.