Evidence map›Paper›PMID 40964606›Full record

ArticleDigital health

Development of an optimized risk evaluation system for cardiovascular-kidney-metabolic syndrome-associated coronary heart disease based on tabular prior-data fitted network.

Shidian Zhu, Hui Zhang, Yanlin Liu, Wenyu Bu, Qiang Wu, Jin Wang, Wandi Chen, Qiannong Wu, Zhirong Geng, Fuming Liu

Abstract read
In one paragraph

Article in Digital health. 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. Article
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

10 authors.

Shidian ZhuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0002-1147-9806
Hui ZhangAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0002-4585-2998
Yanlin LiuAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0006-1778-5037
Wenyu BuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0009-6010-8367
Qiang WuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0005-8409-8256
Jin WangDepartment of Traditional Chinese Medicine, The Second Hospital of Tianjin Medical University, Tianjin, China.ORCID https://orcid.org/0009-0007-7644-4053
Wandi ChenAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0006-3156-4927
Qiannong WuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0007-2627-5669
Zhirong GengAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0003-3766-9034
Fuming LiuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Jiangsu Joint International Laboratory of Animal-Derived Chinese Medicine and Functional Peptides, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0003-4900-4945

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The innovative concept of cardiovascular-kidney-metabolic (CKM) syndrome and tabular prior-data fitted network (TabPFN) offers opportunities for optimizing coronary heart disease (CHD) risk evaluation. This study compared TabPFN with traditional machine learning (ML) methods in medical small-sample data, aiming to construct and validate a risk model for coronary stenosis in CKM-CHD patients. Methods: The research strictly adheres to transparent reporting of a multivariable prediction model for individual prognosis or diagnosis + artificial intelligence (TRIPOD + AI). A total of 296 inpatients from the Main Campus of Jiangsu Province Hospital of Chinese Medicine (June 2023-August 2024) and Zidong Branch (June 2024-December 2024) were screened. The data of the Main Campus were randomly divided into a training set ( Results: Five risk factors were identified: coronary computed tomography angiography, Type 2 diabetes mellitus, triglyceride-glucose index, body mass index, and absolute lymphocyte count. TabPFN outperformed traditional models in small samples, with area under the receiver operating characteristic curve (AUC) values of 0.922 (95% confidence interval [CI]: 0.886-0.958) in the training set, 0.857 (95% CI: 0.733-0.981) in the internal validation set, and 0.815 (95% CI: 0.711-0.918) in the external validation set. The best model reduced the false-negative rate of CCTA by 4.9% (95% CI: 1.9%-8.1%), and a user-friendly Shiny calculator was deployed. Conclusion: TabPFN shows promise in medical small-sample analysis, and the optimized CKM-CHD risk model offers a certain degree of support for clinical decision-making. However, future larger-sample, multicenter prospective studies are still needed to further optimize the model.

Indexed as

cardiovascular-kidney-metabolic syndromediagnostic modellocal shiny calculatorTabPFN

Identifiers

PMID40964606
PMCPMC12437168

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.