Evidence map›Paper›PMID 40451929›Full record

ArticleScientific reports2025

Identification and validation of inflammatory response genes linking chronic kidney disease with coronary artery disease based on bioinformatics and machine learning.

Binhong Yang, Xinyue Yang, Haoqi Sun, Meijuan Cheng, Jingjing Jin, Yunhui Wu, Qi An, Kaixing Yan, Shenglei Zhang, Yaling Bai and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

11 authors.

Binhong YangDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Xinyue YangDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Haoqi SunDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Meijuan ChengDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Jingjing JinDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Yunhui WuDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Qi AnDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Kaixing YanDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Shenglei ZhangDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Yaling BaiDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Jinsheng XuDepartment of Nephrology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China. 46400262@hebmu.edu.cn.

Funding

Natural Science Foundation of Hebei Province H2023206385
6 · The paper itself

Abstract

Coronary artery disease (CAD) commonly occurs and elevates the risk of cardiovascular events and mortality in chronic kidney disease (CKD) patients. The underlying pathogenesis of CKD-related CAD is believed to be closely linked to inflammatory responses. Here, we explored inflammation-related markers for early diagnosis and management of CAD in CKD patients. Through comprehensive bioinformatics analysis and machine learning techniques, glutamate cysteine ligase modifier subunit (GCLM), nuclear protein 1 (NUPR1), and prostaglandin E receptor 1 (PTGER1) were selected as hub biomarkers. Furthermore, GCLM and NUPR1 were demonstrated significantly upregulated in the two validation cohorts of CKD patients with or without hemodialysis, while the change in PTGER1 was not prominent. Additionally, GCLM and NUPR1 were identified as promising indicators to predict CAD in CKD patients. Our study deciphered the higher predictive genes for CAD associated with CKD that is related to inflammation, which provides novel insights into the diagnosis and therapeutic options.

Indexed as

Computational BiologyCoronary Artery DiseaseInflammationMachine LearningRenal Insufficiency, ChronicAgedBasic Helix-Loop-Helix ProteinsBiomarkersFemaleHumansMaleMiddle AgedBasic Helix-Loop-Helix ProteinsBiomarkersChronic kidney diseaseCoronary artery diseaseDiagnostic markersGene expressionInflammation response

Identifiers

PMID40451929
PMCPMC12127440

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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.