Evidence map›Paper›PMID 28595632›Full record

ArticleDiagnostic pathology2017

A comparison of gene expression profiles in patients with coronary artery disease, type 2 diabetes, and their coexisting conditions.

Rui Gong, Menghui Chen, Cuizhao Zhang, Manli Chen, Haibin Li

Open access · goldAbstract readComparative Study
In one paragraph

Article in Diagnostic pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
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  8. Circular RNA profile in coronary artery disease.American journal of translational research · 2019
    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

5 authors at 2 institutions in 1 country.

Rui GongDepartment of gerontology, The Third Municipal Hospital of Shijiazhuang City, Shijiazhuang, Hebei province, 050011, China.
Menghui ChenDepartment of cardiothoracic surgery, The Third Municipal Hospital of Shijiazhuang City, Shijiazhuang, Hebei province, 050011, China.
Cuizhao ZhangMedical laboratory technology, The Third Municipal Hospital of Shijiazhuang City, Shijiazhuang, Hebei province, 050011, China.
Manli ChenDepartment of gerontology, The Third Municipal Hospital of Shijiazhuang City, Shijiazhuang, Hebei province, 050011, China.
Haibin LiDepartment of Cardiology, The Third Affiliated Hospital of Hebei Medical University, Shijiazhuang, Hebei province, 050051, China. haibin_li996@163.com.
First Hospital of Shijiazhuang · CNHebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo support a hypothesis that there is an intrinsic interplay between coronary artery disease (CAD) and type 2 diabetes (T2D), we used RNA-seq to identify unique gene expression signatures of CAD, T2D, and coexisting conditions.

methodsAfter transcriptome sequencing, differential expression analysis was performed between each disordered state and normal control group. By comparing gene expression profiles of CAD, T2D, and coexisting conditions, common and specific patterns of each disordered state were displayed. To verify the specific gene expression patterns of CAD or T2D, the gene expression data of GSE23561 was extracted.

resultsA strong overlap of 191 genes across CAD, T2D and coexisting conditions, were mainly involved in a viral infectious cycle, anti-apoptosis, endocrine pancreas development, innate immune response, and blood coagulation. In T2D-specific PPI networks involving 64 genes, TCF7L2 (Degree = 169) was identified as a key gene in T2D development, while in CAD-specific PPI networks involving 64 genes, HIF1A (Degree = 124), SMAD1 (Degree = 112) and SKIL (Degree = 94) were identified as key genes in the CAD development. Interestingly, with the provided expression data from GSE23561, the three genes were all up-regulated in CAD, and SMAD1 and SKIL were specifically differentially expressed in CAD, while HIF1A was differentially expressed in both CAD and T2D, but with opposite trends.

conclusionsThis study provides some evidences in transcript level to uncover the association of T2D, CAD and coexisting conditions, and may provide novel drug targets and biomarkers for these diseases.

Indexed as

Gene Expression ProfilingGenetic Predisposition to DiseaseBiomarkersCase-Control StudiesCoronary Artery DiseaseDiabetes Mellitus, Type 2HumansPolymorphism, Single NucleotideTranscriptomeBiomarkersCoronary artery diseaseGene expression profileType 2 diabetes

Identifiers

PMID28595632
PMCPMC5465468
OpenAlexW2622212419

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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 OpenQuestion graph.