Evidence map›Paper›PMID 31794148›Full record

ArticleClinical and translational science2020

Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets.

Kai Xue, Jingpu Yang, Yin Zhao, Jinzhang Cheng, Zonggui Wang

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Nasal upregulation ofERJ open research · 2021
    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 1 institution in 1 country.

Kai XueDepartment of Otolaryngology-Head and Neck Surgery, The Second Hospital of Jilin University, Changchun, China.
Jingpu YangDepartment of Otolaryngology-Head and Neck Surgery, The Second Hospital of Jilin University, Changchun, China.
Yin ZhaoDepartment of Otolaryngology-Head and Neck Surgery, The Second Hospital of Jilin University, Changchun, China.
Jinzhang ChengDepartment of Otolaryngology-Head and Neck Surgery, The Second Hospital of Jilin University, Changchun, China.
Zonggui WangDepartment of Otolaryngology-Head and Neck Surgery, The Second Hospital of Jilin University, Changchun, China.
Second Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As an extremely prevalent disease worldwide, allergic rhinitis (AR) is a condition characterized by chronic inflammation of the nasal mucosa. To identify the finer molecular mechanisms associated with the AR susceptibility genes, differentially expressed genes (DEGs) in AR were investigated. The DEG expression and clinical data of the GSE19187 data set were used for weighted gene co-expression network analysis (WGCNA). After the modules related to AR had been screened, the genes in the module were extracted for Gene Ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, whereby the genes enriched in the KEGG pathway were regarded as the pathway-genes. The DEGs in patients with AR were subsequently screened out from GSE19187, and the sensitive genes were identified in GSE18574 in connection with the allergen challenge. Two kinds of genes were compared with the pathway-genes in order to screen the AR susceptibility genes. Receiver operating characteristic (ROC) curve was plotted to evaluate the capability of the susceptibility genes to distinguish the AR state. Based on the WGCNA in the GSE19187 data set, 10 co-expression network modules were identified. The correlation analyses revealed that the yellow module was positively correlated with the disease state of AR. A total of 89 genes were found to be involved in the enrichment of the yellow module pathway. Four genes (CST1, SH2D1B, DPP4, and SLC5A5) were upregulated in AR and sensitive to allergen challenge, whose potentials were further confirmed by ROC curve. Taken together, CST1, SH2D1B, DPP4, and SLC5A5 are susceptibility genes to AR.

Indexed as

Genetic Predisposition to DiseaseBiomarkersComputational BiologyDatasets as TopicDipeptidyl Peptidase 4Gene Expression ProfilingGene Expression RegulationGene Regulatory NetworksHumansNasal MucosaOligonucleotide Array Sequence AnalysisPredictive Value of TestsRhinitis, AllergicRisk AssessmentROC CurveSalivary CystatinsBiomarkersCST1 protein, humanDipeptidyl Peptidase 4DPP4 protein, humanSalivary CystatinsSH2D1B protein, humanSodium-Iodide SymportersSymportersTranscription Factors

Identifiers

PMID31794148
PMCPMC6951973
OpenAlexW2991886373

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.