Evidence map›Paper›PMID 38451044›Full record

ArticleJournal of cellular and molecular medicine2024

Identification of key biomarkers for predicting CAD progression in inflammatory bowel disease via machine-learning and bioinformatics strategies.

Xiaoqi Tang, Yufei Zhou, Zhuolin Chen, Chunjiang Liu, Zhifeng Wu, Yue Zhou, Fan Zhang, Xuanyuan Lu, Liming Tang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. THSD7A Exacerbates Atherosclerosis via Activation of Signaling Axis αvβ3/CEBPD/IL1A.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

9 authors at 4 institutions in 1 country.

Xiaoqi TangSchool of Medicine, Shaoxing University, Zhejiang, China.ORCID 0000-0003-0209-4867
Yufei ZhouDepartment of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Zhuolin ChenDepartment of Orthopedics, Shaoxing People's Hospital (Zhejiang University School of Medicine), Shaoxing, China.
Chunjiang LiuDepartment of General Surgery, Division of Vascular Surgery, Shaoxing People's Hospital, Shaoxing, China.
Zhifeng WuSchool of Medicine, Shaoxing University, Zhejiang, China.
Yue ZhouDepartment of General Surgery, Division of Vascular Surgery, Shaoxing People's Hospital, Shaoxing, China.
Fan ZhangSchool of Medicine, Shaoxing University, Zhejiang, China.
Xuanyuan LuDepartment of Orthopedics, Shaoxing People's Hospital (Zhejiang University School of Medicine), Shaoxing, China.ORCID 0000-0001-9495-4857
Liming TangDepartment of General Surgery, Division of Vascular Surgery, Shaoxing People's Hospital, Shaoxing, China.ORCID 0000-0003-2518-3037
Shaoxing People's Hospital · CNShaoxing University · CNFudan University · CNSun Yat-sen University · CN

Funding

The Natural Science Foundation of Zhejiang Province LGF22H060031The Shaoxing Scientific and Technological Program of Zhejiang Province 2022KY032
6 · The paper itself

Abstract

The study aimed to identify the biomarkers for predicting coronary atherosclerotic lesions progression in patients with inflammatory bowel disease (IBD). Related transcriptome datasets were seized from Gene Expression Omnibus database. IBD-related modules were identified via Weighted Gene Co-expression Network Analysis. The 'Limma' was applied to screen differentially expressed genes between stable coronary artery disease (CAD) and acute myocardial infarction (AMI). Subsequently, we employed protein-protein interaction (PPI) network and three machine-learning strategies to further screen for candidate hub genes. Application of the receiver operating characteristics curve to quantitatively evaluate candidates to determine key diagnostic biomarkers, followed by a nomogram construction. Ultimately, we performed immune landscape analysis, single-gene GSEA and prediction of target-drugs. 3227 IBD-related module genes and 570 DEGs accounting for AMI were recognized. Intersection yielded 85 shared genes and mostly enriched in immune and inflammatory pathways. After filtering through PPI network and multi-machine learning algorithms, five candidate genes generated. Upon validation, CTSD, CEBPD, CYP27A1 were identified as key diagnostic biomarkers with a superior sensitivity and specificity (AUC > 0.8). Furthermore, all three genes were negatively correlated with CD4

Indexed as

Coronary Artery DiseaseInflammatory Bowel DiseasesMyocardial InfarctionBiomarkersComputational BiologyHumansMachine LearningBiomarkersacute myocardial infarctionatherosclerosis progressionbioinformaticscoronary artery diseaseinflammation and immunityinflammatory bowel diseasemachine-learning

Identifiers

PMID38451044
PMCPMC10919158
OpenAlexW4392561511

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.