Evidence map›Paper›PMID 36092962›Full record

ArticleDisease markers2022

Gene-Based Network Analysis Reveals Prognostic Biomarkers Implicated in Diabetic Tubulointerstitial Injury.

Sumin Wu, Wei Li, Binhuan Chen, Xuefeng Pei, Yangjian Cao, Yuting Wei, Ye Zhu

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 8 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

7 authors at 1 institution in 1 country.

Sumin WuDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.ORCID https://orcid.org/0000-0002-0213-0701
Wei LiDepartment of Pathology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.
Binhuan ChenDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.
Xuefeng PeiDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.
Yangjian CaoDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.
Yuting WeiDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.ORCID https://orcid.org/0000-0002-8632-1811
Ye ZhuDepartment of Nephrology, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China.ORCID https://orcid.org/0000-0002-8535-5323
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diabetic nephropathy (DN), a significant cause of chronic kidney disease (CKD), is a devastating disease worldwide. Objective: The aim of this study was to reveal crucial genes closely linked to the molecular mechanism of tubulointerstitial injury in DN. Methods: The Gene Expression Omnibus (GEO) database was used to download the datasets. Based on this, a weighted gene coexpression network analysis (WGCNA) network was constructed to detect DN-related modules and hub genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichments were performed on the selected hub genes and modules. Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was performed on the obtained gene signature. Results: The WGCNA network was constructed based on 3019 genes, and nine gene coexpression modules were generated. A total of 57 genes, including 34 genes in the magenta module and 23 genes in the purple module, were adapted as hub genes. 61 significantly downregulated and 119 upregulated genes were screened as differentially expressed genes (DEGs). 25 overlapping genes between hub genes chosen from WGCNA and DEG were identified. Through LASSO analysis, a 9-gene signature may be a potential prognostic biomarker for DN. To further explore the potential mechanism of DN, the different immune cell infiltrations between tubulointerstitial samples of DN and healthy samples were estimated. Conclusions: This bioinformatics study identified CX3CR1, HRG, LTF, TUBA1A, GADD45B, PDK4, CLIC5, NDNF, and SOCS2 as candidate biomarkers for the diagnosis of DN. Moreover, DN tends to own a higher proportion of memory B cell.

Indexed as

Diabetes MellitusGene Expression ProfilingBiomarkersGene Regulatory NetworksHumansPrognosisBiomarkers

Identifiers

PMID36092962
PMCPMC9452978
OpenAlexW4294540862

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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.