Evidence map›Paper›PMID 35173843›Full record

ArticleAmerican journal of translational research2022

Gene expression analysis reveals immune and metabolic candidate pathways in the pathogenesis of chronic otitis media.

Siran Lin, Wei Zhang, Yuzhen Xu, Qianqian Liu, Wenhong Zhang, Lingyun Shao

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Siran LinDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Wei ZhangDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Yuzhen XuDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Qianqian LiuDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Wenhong ZhangDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Lingyun ShaoDepartment of Infectious Diseases, Huashan Hospital, Fudan University Shanghai 200040, China.
Huashan Hospital · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesChronic otitis media (COM) is a common disease and causes significant hearing impairment in many adults. Our study aimed to investigate the immune response in COM adult patients through RNA sequencing.

methodsIn this study, we enrolled four adult COM patients and five healthy controls (HCs) to analyze and compare the mRNA signatures in their peripheral blood mononuclear cells (PBMCs). Gene Ontology functional enrichment and Kyoto Encyclopedia of Genes and Genomes pathway analyses were performed on the differentially expressed genes between the COM patients and the HCs. Furthermore, the immune cell proportions of the two groups were estimated by CIBERSORT. The GSE125532, GSE27990, and GSE23140 gene expression profiles were also retrieved and analyzed for comparison with our results.

resultsMany immune pathways and genes were upregulated in the COM patients, including the IL-17 pathway and NLRP3. Monocytes and macrophages increased (P=0.005 and P=0.033, respectively), and the CD8+ T cells decreased (P=0.033) in the COM patients compared to the HCs. The COM patients' signatures also reflected a hypoxic state.

conclusionsOur findings emphasized the roles of several immune pathways and a hypoxic state in interpreting host responses during COM, and may enable the development of novel therapeutic tools for the disease.

Indexed as

Chronic otitis mediadifferentially expressed genesfunctional enrichment analysishypoxiaimmune cell proportions

Identifiers

PMID35173843
PMCPMC8829611
OpenAlexW4213392872

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.