Evidence map›Paper›PMID 41781159›Full record

ArticleRMD open2026

Machine learning-based multiclass model for autoimmune disease diagnosis and classification through nailfold videocapillaroscopy features.

Jie Li, Congcong Jian, Jiaojiao Zhao, Zhuming Yin, Xue Li, Chaochun Song, Hongjun Zhou, Wenzhang Chen, Qin Liu, Jie Zhang and 11 more

Abstract read
In one paragraph

Article in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

21 authors.

Jie Li *Department of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Congcong Jian *Department of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Jiaojiao Zhao *Department of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Zhuming YinTianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Xue LiDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Chaochun SongDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Hongjun ZhouDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Wenzhang ChenDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Qin LiuDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Jie ZhangDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Zhengzhong TangDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Xiangyi XiongSouthwest Medical University, Luzhou, China.
Yuqi LiuCollege of Computer and Information Science, School of Software, Southwest University, Chongqing, China.
Jun ZhouDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Xue YangDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China.
Jianhong WuDepartment of Rheumatology and Immunology, Dazhou Central Hospital, Dazhou, China.
Tingting WangDepartment of Rheumatology and Immunology, Dazhou Central Hospital, Dazhou, China.
Qinghua ZouDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Army Medical University, Chongqing, China zengfx@pku.edu.cn zouqinghua318@tmmu.edu.cn openmind999@163.com shuhuae76@163.com.
Yong ZhangDepartment of Rehabilitation Medicine, People's Hospital Affiliated to Chongqing Three Gorges Medical College, Chongqing, China zengfx@pku.edu.cn zouqinghua318@tmmu.edu.cn openmind999@163.com shuhuae76@163.com.
Hua'e ShuDepartment of Hematology, Rheumatology and Immunology, The People's Hospital of Kaizhou District, Chongqing, China zengfx@pku.edu.cn zouqinghua318@tmmu.edu.cn openmind999@163.com shuhuae76@163.com.
Fanxin ZengDepartment of Clinical Research Center, Sichuan Clinical Research Center for Medical Imaging, Dazhou Central Hospital, Dazhou, China zengfx@pku.edu.cn zouqinghua318@tmmu.edu.cn openmind999@163.com shuhuae76@163.com.ORCID 0000-0002-7337-4463

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop and validate a predictive model for distinguishing controls (Ctr), rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) based on nailfold videocapillaroscopy (NVC) image features.

methodsA total of 600 NVC images from 396 participants (Ctr=117, RA=337 and SLE=146) were collected and divided into training and test sets at a 7:3 ratio. Nine NVC features were extracted, and an eXtreme Gradient Boosting multiclassification model was constructed to distinguish the three groups. SHapley Additive exPlanations (SHAP) analysis was performed to evaluate feature importance and interpret the model.

resultsSeven NVC features showed significant differences among the groups. The model achieved macro area under the curve values of 0.96 and 0.80 in the training and test sets, respectively. SHAP analysis identified papilla shape, red blood cell aggregation, number of capillary loops, number of crossed capillary loops and subpapillary venous plexus (SVP) as key features among the groups. Each group was characterised by specific NVC patterns. In Ctr, papilla shape emerged as the key feature and showed correlations with neutrophils, white blood cells and monocytes. In patients with RA, the number of crossed capillary loops was the most prominent feature and correlated with erythrocyte sedimentation rate, complement levels (C3 and C4) and inversely with immunoglobulin G. In patients with SLE, the SVP was the dominant feature and effectively distinguished SLE from both Ctr and RA.

conclusionsThis study developed a robust multiclassification model for differentiating autoimmune diseases using NVC features. The findings enhance our understanding of microvascular alterations and provide a potential tool for clinical diagnosis and disease monitoring.

Indexed as

Autoimmune DiseasesMachine LearningMicroscopic AngioscopyNailsAdultArthritis, RheumatoidCapillariesClassification AlgorithmsFemaleHumansLupus Erythematosus, SystemicMaleMiddle AgedROC CurveArthritis, RheumatoidAutoimmune DiseasesLupus Erythematosus, SystemicMachine Learning

Identifiers

PMID41781159
PMCPMC12970066

What OpenQuestion holds

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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.