Evidence map›Paper›PMID 32714363›Full record

ArticleFrontiers in genetics2020

Identification of Four Potential Biomarkers Associated With Coronary Artery Disease in Non-diabetic Patients by Gene Co-expression Network Analysis.

Min Jiao, Jingtian Li, Quan Zhang, Xiufeng Xu, Ruidong Li, Peikang Dong, Chun Meng, Yi Li, Lijuan Wang, Wanpeng Qi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  9. Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis.Liver international : official journal of the International Association for the Study of the Liver · 2021
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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

13 authors at 3 institutions in 2 countries.

Min JiaoDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Jingtian LiDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Quan ZhangDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Xiufeng XuDepartment of Neurology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Ruidong LiGraduate Program in Genetics, Genomics, and Bioinformatics, University of California, Riverside, Riverside, CA, United States.
Peikang DongDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Chun MengDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Yi LiDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Lijuan WangDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Wanpeng QiDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Kai KangDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Hongjie WangDivision of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Tao WangDepartment of Cardiology, Affiliated Hospital of Weifang Medical University, Weifang, China.
Weifang Medical University · CNTongji Hospital · CNUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary artery disease (CAD) is a type of cardiovascular disease that greatly hurts the health of human beings. Diabetic status is one of the largest clinical factors affecting CAD-associated gene expression changes. Most of the studies focus on diabetic patients, whereas few have been done for non-diabetic patients. Since the pathophysiological processes may vary among these patients, we cannot simply follow the standard based on the data from diabetic patients. Therefore, the prognostic and predictive diagnostic biomarkers for CAD in non-diabetic patient need to be fully recognized. MATERIALS AND

methodsTo screen out candidate genes associated with CAD in non-diabetic patients, weighted gene co-expression network analysis (WGCNA) was constructed to conduct an analysis of microarray expression profiling in patients with CAD. First, the microarray data GSE20680 and GSE20681 were downloaded from NCBI. We constructed co-expression modules

resultsThe results showed that the midnight blue module and the yellow module played vital roles in the pathogenesis of CAD in non-diabetic patients. Additionally, CD40, F11R, TNRC18, and calcium/calmodulin-dependent protein kinase type II gamma (CAMK2G) were screened out and validated using enzyme-linked immunosorbent assay (ELISA) in an independent patient cohort and immunohistochemical (IHC) staining in an atherosclerosis mouse model.

conclusionOur findings demonstrate that hub genes, CD40, F11R, TNRC18, and CAMK2G, are surrogate diagnostic biomarkers and/or therapeutic targets for CAD in non-diabetic patients and require deeper validation.

Indexed as

biomarkerscoronary artery diseasefunction enrichment analysisnon-diabetic patientsweighted gene co-expression network analysis

Identifiers

PMID32714363
PMCPMC7344232
OpenAlexW3036731955

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