Evidence map›Paper›PMID 42112773›Full record

ArticleBioMed research international2026

Exploring Immune-Related Gene and Mechanisms in Rosacea Through Transcriptome Analysis and Mendelian Randomization.

Yafang Wang, Jian Zhang

Abstract read
In one paragraph

Article in BioMed research international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

2 authors.

Yafang WangThe First People's Hospital of Yinchuan, Yinchuan, Ningxia, China.
Jian ZhangThe First People's Hospital of Yinchuan, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0002-5059-2847

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysregulation of the innate and adaptive immune system is thought to be central to the pathogenesis of rosacea. However, the molecular mechanism of immune-related genes has not been extensively studied in rosacea.

methodsThe GSE65914 and GSE155141 datasets were included in this study. Firstly, intersection genes were screened by overlapping key module genes obtained from weighted gene coexpression network analysis (WGCNA) and DEGs (rosacea vs. control). Then, functional enrichment analysis was performed to explore the functions of intersection genes. Subsequently, exposure factors (key genes) for rosacea were identified through Mendelian randomization (MR), and machine learning and expression analysis were conducted based on intersection genes. Single-gene gene set enrichment analysis (GSEA) was utilized to investigate the molecular mechanisms of key genes. Additionally, a regulatory network was constructed. Finally, the mRNA-drug interaction network was established.

resultsA total of 624 intersection genes were screened, with functional enrichment results indicating involvement in positive regulation of protein kinase activity and the Hippo signaling pathway. Four key genes (ALDH1A1, COL17A1, RELL1, and ZNF404) were identified, with ALDH1A1 as a risk factor and the others as protective factors for rosacea. Single-gene GSEA results showed enrichment in the IL-17 and chemokine signaling pathways. The regulatory network included four mRNAs, two transcription factors (TFs), and 61 miRNAs. Lastly, 73 drugs targeting key genes were predicted.

conclusionsThis study identified four immune-related key genes (ALDH1A1, COL17A1, RELL1, and ZNF404) through MR analysis and machine learning, suggesting potential diagnostic or therapeutic candidates for further validation.

Indexed as

Mendelian Randomization AnalysisRosaceaTranscriptomeGene Expression ProfilingGene Regulatory NetworksHumansimmunityMendelian randomizationrosaceatreatment

Identifiers

PMID42112773
PMCPMC13159088

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