Evidence map›Paper›PMID 41225023›Full record

ArticleAnnals of hematology2025

Development of an artificial intelligence-based early diagnostic system for light-chain amyloidosis.

Wei Yan, Jian Chen, Tao He, Haoze Xu, Jianmin Chen, Xiaoyu Liu, Liye Zhong, Yan Li, Chunyan Sun, Xiaobo Wang and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

19 authors.

Wei Yan *Department of Hematology, Shengjing Hospital, China Medical University, No. 39 Huaxiang Road, Shenyang, 110004, China.
Jian Chen *School of Computer Science and Engineering, Northeastern University, Shenyang, China.
Tao HeChina Neusoft Research Institute, Northeastern University, Shenyang, China.
Haoze XuSchool of Computer Science and Engineering, Northeastern University, Shenyang, China.
Jianmin ChenSchool of Computer Science and Engineering, Northeastern University, Shenyang, China.
Xiaoyu LiuDepartment of Hematology, Shengjing Hospital, China Medical University, No. 39 Huaxiang Road, Shenyang, 110004, China.
Liye ZhongDepartment of Hematology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Yan LiDepartment of Hematology, The People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Chunyan SunDepartment of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xiaobo WangDepartment of Hematology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Li GaoMedical Center of Hematology, Xinqiao Hospital, State Key Laboratory of Trauma, Burn and Combined Injury, Army Medical University, Chongqing, China.
Fengyan JinDepartment of Hematology, Cancer Center, the First Hospital of Jilin University, Changchun, China.
Bingzong LiDepartment of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Chunrui LiDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yingyou WenChina Neusoft Research Institute, Northeastern University, Shenyang, China.
Zhuo ChenDepartment of Hematology, The fourth Affiliated Hospital of China Medical University, Shenyang, China.
Boheng LiuInformation Science and Engineering, Northeastern University, Shenyang, China.
Jian Li *Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. lijian@pumch.cn.
Huihan Wang *Department of Hematology, Shengjing Hospital, China Medical University, No. 39 Huaxiang Road, Shenyang, 110004, China. wanghh@sj-hospital.org.

Funding

Key R&D Program of Liaoning Province 2019JH2/10100027National Natural Science Foundation of China Nos. 61972079 and 61772126Natural Science Foundation of Liaoning Province 2022-YGJC-61;2022-MS-219Shingling Liao Ning Revitalization Talents Program XLYC1802100
6 · The paper itself

Abstract

Light-chain (AL) amyloidosis is a rare disease and its early diagnosis remains challenging. This study aimed to develop an artificial intelligence (AI)-based diagnostic assistance system to improve the early diagnosis of AL amyloidosis and facilitate earlier and more precise disease management. Through cooperation with 18 hospitals in the Chinese Registration Network for Light-chain Amyloidosis (CRNLA), 1,355 patients with AL amyloidosis were registered and followed up from January 2010 to January 2022. Ten variables that are easily monitored in clinics, including age, cardiac troponin I (cTnl), N-terminal prohormone B-type natriuretic peptide (NT-ProBNP), creatinine (Crea), albumin (ALB), total bilirubin (Tbil), alkaline phosphatase (ALP), interventricular septum (IVS), left ventricular posterior wall (LVPW), and ejection fraction (EF), were selected. An early assistant diagnostic model of AL amyloidosis was established using gradient boosting decision tree (GBDT), support vector machine (SVM), random forest (RF), and ensemble learning models. A validation subset of challenging cases from the external validation set was used to compare the performance of the AI-based early diagnostic assistance system to that of physicians. All of the typical machine learning algorithms, namely the GBDT, SVM, RF, and ensemble learning models, performed well. The ensemble learning model was considered to have the best performance in the external validation set based on its highest F1 value (0.94) and an area under the receiver operating characteristic (ROC) curve of 0.9784 (95% confidence interval [CI]:0.963-0.987). Performance comparisons between the AI-based early diagnostic assistance model and physicians suggested that the diagnostic accuracy of the AI model (0.95,95%CI:0.92-0.98;P < 0.05) substantially exceeded that of the hematologists (0.73,95%CI:0.7-0.82) and other physicians (0.65,95%CI: 0.61-0.71). The model established by AI, which uses routine laboratory and echocardiography results, can predict the possibility of AL amyloidosis in various scenarios, which may support the early diagnosis of this rare disease.

Indexed as

Artificial IntelligenceImmunoglobulin Light-chain AmyloidosisAdultAgedEarly DiagnosisFemaleHumansMachine LearningMaleMiddle AgedSupport Vector MachineArtificial intelligenceEarly diagnosisEnsemble learning modelsLight chain amyloidosis

Identifiers

PMID41225023
PMCPMC12764643

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.