Evidence map›Paper›PMID 29439675›Full record

ArticleBMC cardiovascular disorders2018

Screening key genes for abdominal aortic aneurysm based on gene expression omnibus dataset.

Li Wan, Jingyong Huang, Haizhen Ni, Guanfeng Yu

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Li WanDepartment of pathology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Jingyong HuangDepartment of vascular surgery, The First Affiliated Hospital of Wenzhou Medical University, NO.3, YuanXi Lane, Lucheng District, Wenzhou, Zhejiang, 325000, China. jingyong_huang@163.com.ORCID 0000-0002-0077-7325
Haizhen NiDepartment of vascular surgery, The First Affiliated Hospital of Wenzhou Medical University, NO.3, YuanXi Lane, Lucheng District, Wenzhou, Zhejiang, 325000, China.
Guanfeng YuDepartment of vascular surgery, The First Affiliated Hospital of Wenzhou Medical University, NO.3, YuanXi Lane, Lucheng District, Wenzhou, Zhejiang, 325000, China.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbdominal aortic aneurysm (AAA) is a common cardiovascular system disease with high mortality. The aim of this study was to identify potential genes for diagnosis and therapy in AAA.

methodsWe searched and downloaded mRNA expression data from the Gene Expression Omnibus (GEO) database to identify differentially expressed genes (DEGs) from AAA and normal individuals. Then, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis, transcriptional factors (TFs) network and protein-protein interaction (PPI) network were used to explore the function of genes. Additionally, immunohistochemical (IHC) staining was used to validate the expression of identified genes. Finally, the diagnostic value of identified genes was accessed by receiver operating characteristic (ROC) analysis in GEO database.

resultsA total of 1199 DEGs (188 up-regulated and 1011 down-regulated) were identified between AAA and normal individual. KEGG pathway analysis displayed that vascular smooth muscle contraction and pathways in cancer were significantly enriched signal pathway. The top 10 up-regulated and top 10 down-regulated DEGs were used to construct TFs and PPI networks. Some genes with high degrees such as NELL2, CCR7, MGAM, HBB, CSNK2A2, ZBTB16 and FOXO1 were identified to be related to AAA. The consequences of IHC staining showed that CCR7 and PDGFA were up-regulated in tissue samples of AAA. ROC analysis showed that NELL2, CCR7, MGAM, HBB, CSNK2A2, ZBTB16, FOXO1 and PDGFA had the potential diagnostic value for AAA.

conclusionsThe identified genes including NELL2, CCR7, MGAM, HBB, CSNK2A2, ZBTB16, FOXO1 and PDGFA might be involved in the pathology of AAA.

Indexed as

Databases, GeneticAortic Aneurysm, AbdominalCase-Control StudiesData MiningGene Expression ProfilingGene Expression RegulationGenetic Association StudiesGenetic MarkersGenetic Predisposition to DiseaseHumansImmunohistochemistryPhenotypePrognosisProtein Interaction MapsSignal TransductionTranscriptomeGenetic Markersabdominal aortic aneurysmbiomarkersgene expressionprotein-protein interaction networkTFs regulatory networktherapy target

Identifiers

PMID29439675
PMCPMC5812227
OpenAlexW2806879279

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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.