Evidence map›Paper›PMID 38223424›Full record

ArticleJournal of inflammation research2024

Immune-Related Genes and Immune Cell Infiltration Characterize the Maturation Status of Arteriovenous Fistulas: An Integrative Bioinformatics Study and Experimental Validation Based on Transcriptome Sequencing.

Peng Lu, Tun Wang, Zicheng Wan, Mo Wang, Yang Zhou, Zhenyu He, Sheng Liao, Haiyang Liu, Chang Shu

Open access · goldAbstract read
In one paragraph

Article in Journal of inflammation research, 2024. 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
0.7field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

9 authors at 3 institutions in 1 country.

Peng Lu *Department of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Tun Wang *Department of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Zicheng WanDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Mo WangDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Yang ZhouDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Zhenyu HeDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Sheng LiaoDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Haiyang LiuDepartment of Geriatrics, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Chang ShuDepartment of Vascular Surgery, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Second Xiangya Hospital of Central South University · CNCentral South University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Arteriovenous fistula (AVF) is the preferred vascular access for hemodialysis, but the low maturation rate is concerning. Immune cells' impact on AVF maturation lacks bioinformatics research. The study aims to investigate the potential predictive role of immune-related genes and immune cell infiltration characteristics in AVF maturation. Patients and Methods: We analyzed the high-throughput sequencing dataset to identify differentially expressed genes (DEGs). Then, we performed enrichment analyses (GO, KEGG, GSEA) on immune-related genes and pathways in mature AVF. We focused on differentially expressed immune-related genes (DEIRGs) and constructed a PPI network to identify hub genes. These hub genes were validated in other databases and experiments, including qPCR and immunohistochemistry (IHC). The immune cell infiltration characteristics in native veins, failed AVFs, and matured AVFs were analyzed by cibersortX. Partial experimental validation was conducted using clinical samples. Results: Our results showed that immune-related genes and signaling pathways are significantly enriched in mature AVF. We validated this in other databases and ultimately identified three hub genes (IL1B, IL6, CXCR4) in combination with experiments. Significant differences in immune cell infiltration characteristics were observed among native veins, failed AVFs, and matured AVFs. Immune cell infiltration analysis revealed that accumulation of CD4+ T cells, dendritic cells, mast cells and M2 macrophages contribute to AVF maturation. These immune-related genes and immune cells have the potential to serve as predictive factors for AVF maturation. We partially validated this experimentally. Conclusion: From a bioinformatics perspective, our results have identified, for the first time, a set of immune-related genes and immune cell infiltration features that can characterize the maturation of AVF and significantly impact AVF maturation. These features hold potential as predictive indicators for AVF maturation outcomes.

Indexed as

AVF maturationbioinformaticsimmune-related genesinflammation

Identifiers

PMID38223424
PMCPMC10785828
OpenAlexW4390655465

What OpenQuestion holds

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LicenceCC BY-NC
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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.