Evidence map›Paper›PMID 41858734›Full record

ArticleFrontiers in molecular biosciences2026

Disease classification via interpretable machine learning based on multi-center routine coagulation test.

Feng Dong, Yaqiong Zhang, Weibu Chen, Changmin Wang, Lei Zhang, Xiaoling Gao, Xiaoli Zhang, Minghua Jiang, Guobin Xu, Ruichuang Yang and 4 more

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Feng Dong *Department of Clinical Laboratory, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Yaqiong Zhang *Department of Clinical Laboratory, Taizhou Key Laboratory of Research and Transformation of Extracellular Vesicles, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang, China.
Weibu Chen *Laboratory Department, Shenzhen People's Hospital, Shenzhen, Guangdong, China.
Changmin WangCenter of Clinical Laboratory, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang, China.
Lei ZhangDepartment of Clinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Xiaoling GaoDepartment of Laboratory Medicine, Hainan General Hospital, Haikou, Hainan, China.
Xiaoli ZhangThe Affiliated Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Minghua JiangThe Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Guobin XuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Clinical Laboratory, Peking University Cancer Hospital and Institute, Beijing, China.
Ruichuang YangShenzhen Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, Guangdong, China.
Yutong HouDepartment of Artificial Intelligence, Beijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, Beijing, China.
Jiandang MaLuoyang Central Hospital, Luoyang, Henan, China.
Chuanbao LiDepartment of Laboratory Medicine, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, China.
Jun WuDepartment of Clinical Laboratory, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study aims to establish an interpretable disease classification model via machine learning and identify key features related to the disease to assist clinical disease diagnosis based on a multi-center CX9000 routine coagulation test. Methods: Data from 11 hospitals were collected. An unsupervised clustering model was used to extract classification patterns, and clinical experts assigned disease labels. Multiple machine learning models, including Random Forest, SVM, Decision Tree, Naive Bayes, MLP, XGBoost, and LightGBM, were trained. Ten-fold cross validation and external validation were performed. For external validation, models were trained with data from 8 hospitals (˜90%) and tested on the remaining 2 hospitals (˜10%). SHAP and Decision Tree analysis were used for interpretability. Results: Clear clustering patterns were observed for valvular heart disease (VHD) and pulmonary infection (PI). LightGBM achieved the best performance in both tasks. In cross validation, the mean F1-scores were 0.8890 and 0.7233, and the mean AUCs were 0.9500 and 0.8023. External validation showed strong generalization, with mean F1-scores of 0.9259 and 0.7464 and mean AUCs of 0.9493 and 0.8297. The sample visualization by t-SNE and the interpretable analysis by SHAP and Decision Trees identified some key classification features, i.e., international normalized ratio (INR) for VHD and age for PI. Conclusion: Machine learning models based on multi-center coagulation tests provide effective and interpretable disease classification, supporting clinical diagnostic automation.

Indexed as

disease classificationinterpretability analysismachine learningmulti-center coagulation testSHapley Additive exPlanations

Identifiers

PMID41858734
PMCPMC12996926

What Socratic holds

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LicenceCC BY
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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 Socratic graph.