Evidence map›Paper›PMID 41103698›Full record

ArticleFrontiers in medicine2025

Development and application of machine learning models for hematological disease diagnosis using routine laboratory parameters: a user-friendly diagnostic platform.

Jingya Liu, Yang Gou, Wuchen Yang, Hao Wang, Jing Zhang, Shengwang Wu, Siheng Liu, Tinglu Tao, Yongjie Tang, Cheng Yang and 7 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

17 authors.

Jingya Liu *Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Yang Gou *Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Wuchen Yang *Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Hao WangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Jing ZhangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Shengwang WuMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Siheng LiuMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Tinglu TaoMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Yongjie TangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Cheng YangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Siyin ChenMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Ping WangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Yimei FengMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Cheng ZhangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Shuiqing LiuMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Xiangui PengMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.
Xi ZhangMedical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: In recent years, with the change of social environment, the incidence and detection rate of hematological diseases have shown an increasing trend. Early diagnosis and detection of hematological diseases are very important to improve the quality of life and prognosis of patients. Methods: In this study, we employed 54 clinical and conventional laboratory parameters. By optimally combining multiple feature selection methods and machine learning algorithms, we developed 7 machine learning models with varying feature set sizes. We comprehensively evaluated the performance of these models, analyzed the interpretability of the optimal and simplified models using SHapley Additive exPlanations (SHAP), and compared these two models with the diagnostic performance of hematologists. Finally, we developed a user-friendly diagnostic platform. Results: The results showed that the ensemble model_1 with 46 feature parameters (EnMod1-46) and the simple ensemble model_2 with 12 feature parameters (EnMod2-12) demonstrated significant performance in diagnosing 16 types of hematological diseases. On the temporally distinct test set_1, the EnMod1-46 achieved an accuracy of 0.804 and an area under the curve (AUC) of 0.964, while EnMod2-12 attained an accuracy of 0.784 and an AUC of 0.961. To further validate the model's generalization performance, EnMod1-46 achieved an accuracy of 0.738 and an AUC of 0.973 on the independent external test set_2, while EnMod2-12 yielded an accuracy of 0.705 and an AUC of 0.962. SHAP analysis showed that PLT, WBC, MCV, HGB, RBC and age were significant parameters in both models. Comparative analysis of clinical diagnosis revealed that the performance of EnMod1-46 and EnMod2-12 outperformed junior hematologists, while EnMod1-46 was comparable to senior hematologists. Concurrently, based on EnMod2-12, we developed a user-friendly diagnostic platform to facilitate risk assessment and improve access to accurate diagnosis. Conclusion: This study provides an efficient and accurate screening method for hematological diseases, especially in resource-limited countries and regions.

Indexed as

diagnostic platformhematological diseaseslaboratory parametersmachine learningprediction modelSHAP

Identifiers

PMID41103698
PMCPMC12521225

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.