Evidence map›Paper›PMID 40831467›Full record

ArticleEClinicalMedicine2025

An artificial intelligence model integrating culprit lesion diagnosis and risk assessment for acute coronary syndrome.

Peng Peng Xu, Bin Hu, Fan Zhou, Zhi Han Xu, Qian Chen, Tong Yuan Liu, Bang Jun Guo, Chang Sheng Zhou, Xin Wei Tao, Hong Yan Qiao and 4 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

14 authors.

Peng Peng XuDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.
Bin HuDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.
Fan ZhouDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.
Zhi Han XuCT Collaboration, Siemens Healthineers, Shanghai, China.
Qian ChenDepartment of Radiology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China.
Tong Yuan LiuDepartment of Radiology, Jinling Hospital, Nanjing Medical University, Nanjing, Jiangsu, 210002, China.
Bang Jun GuoDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.
Chang Sheng ZhouDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.
Xin Wei TaoDepartment of Interventional Oncology, Boston Scientific Corporation, 200023, Shanghai, China.
Hong Yan QiaoDepartment of Medical Imaging, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu, 214122, China.
Jia Ni ZouDepartment of Diagnostic Radiology, General Hospital of Central Theater Command of the PLA, Wuhan, Hubei, 430070, China.
Xiang Ming FangDepartment of Radiology, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, Jiangsu, 214023, China.
Wen Cai HuangDepartment of Diagnostic Radiology, General Hospital of Central Theater Command of the PLA, Wuhan, Hubei, 430070, China.
Long Jiang ZhangDepartment of Radiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, 210002, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: An integrated machine learning (ML) approach capable of both diagnosing acute coronary syndrome (ACS, encompassing myocardial infarction and unstable angina) and predicting future ACS risk within defined optimal timeframes remains an unmet need in cardiovascular risk stratification. Methods: We conducted a multicentre cohort study in China between January 2012 and December 2021. The derivation cohort (cohort 1+ cohort 2), consisting of a training, validation, and independent external test set, retrospectively included 1854 patients from four hospitals who underwent coronary computed tomography angiography (CCTA) and received a definitive diagnosis of ACS or chronic coronary syndromes (CCS) within 7 days. The diagnostic performance of five commonly used ML algorithms for identifying ACS culprit lesions was developed and compared within this cohort. After selecting the optimal ML model, its performance was further validated in a single-center prospective cohort (cohort 3) and a nested case-control cohort (cohort 4) from two multicenter prospective cohorts to assess its ability to predict future ACS risk stratification (≥30 days). Findings: The derivation cohort comprised 1854 participants, among whom 281 experienced new-onset ACS within 7 day. The single-centre prospective cohort included 563 participants, of whom 23 developed ACS during follow-up (median 60.0 months). The nested case-control cohort included 202 participants, of whom 43 developed ACS during follow-up (median 28.0 months). In the derivation cohort, the random forest (RF) model demonstrated the best diagnostic performance and robustness among the five ML algorithms for detecting ACS culprit lesions, achieving an area under the receiver operating characteristic curve (AUC) of 0.85 across the training (95% confidence interval [Cl]: 0.82-0.89), validation (95% Cl: 0.80-0.90), and test sets (95% Cl: 0.78-0.92). In two prospective cohorts, Kaplan-Meier curves showed that the RF model successfully stratified the risk of future ACS events (both log-rank Interpretation: The ACS culprit lesion model developed using RF algorithms demonstrated superior diagnostic performance and was effective for short-term (2-year) ACS risk stratification. Funding: This work was supported by the Noncommunicable Chronic Diseases-National Science and Technology Major Project (2024ZD0521700), and the National Natural Science Foundation of China (No. 82441019 for L.J. Z.).

Indexed as

Acute coronary syndromeComputed tomography angiographyMachine learningRandom forestRisk stratification

Identifiers

PMID40831467
PMCPMC12359167

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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.