Evidence map›Paper›PMID 38661482›Full record

ArticleClinical and experimental immunology2024

Exploring the causal role of immune cells in cerebral aneurysm through single-cell transcriptomics and Mendelian randomization analysis.

Yunhu Yu, Shiao Tong, Tao Liu, Yunpeng Cai, Yuanmei Song, Hang Zhou, Rongcai Jiang

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 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
0.5field-weighted citation impact, top 37% 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, 2 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

7 authors at 2 institutions in 1 country.

Yunhu YuDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.
Shiao TongDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.ORCID 0000-0001-9721-0845
Tao LiuDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.ORCID 0000-0002-0506-3356
Yunpeng CaiDepartment of Neurosurgery, the People's Hospital of HongHuaGang District of ZunYi, Zunyi, China.ORCID 0009-0003-4804-7916
Yuanmei SongDepartment of Neurosurgery, the People's Hospital of HongHuaGang District of ZunYi, Zunyi, China.ORCID 0000-0003-0416-6430
Hang ZhouDepartment of Neurosurgery, the People's Hospital of HongHuaGang District of ZunYi, Zunyi, China.ORCID 0000-0003-3867-4257
Rongcai JiangDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.ORCID 0009-0002-0851-3786
Tianjin Medical University General Hospital · CNFirst People’s Hospital of Zunyi · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral aneurysm (CA) represents a significant clinical challenge, characterized by pathological dilation of cerebral arteries. Recent evidence underscores the crucial involvement of immune cells in CA pathogenesis. This study aims to explore the complex interplay between immune cells and CA formation. We analyzed single-cell RNA sequencing data from the GSE193533 dataset, focusing on unruptured CA and their controls. Comprehensive cell-type identification and pseudo-time trajectory analyses were conducted to delineate the dynamic shifts in immune cell populations. Additionally, a two-sample Mendelian randomization (MR) approach was employed to investigate the causal influence of various immunophenotypes on CA susceptibility and the reciprocal effect of CA formation on immune phenotypes. Single-cell transcriptomic analysis revealed a progressive loss of vascular smooth muscle cells (VSMCs) and an increase in monocytes/macrophages (Mo/MΦ) and other immune cells, signifying a shift from a structural to an inflammatory milieu in CA evolution. MR analysis identified some vital immunophenotypes, such as CD64 on CD14+ CD16+ monocytes (OR: 1.236, 95% CI: 1.064-1.435, P = 0.006), as potential risk factors for CA development, while others, like CD28- CD8br %CD8br (OR: 0.883, 95% CI: 0.789-0.988, P = 0.030), appeared protective. Reverse MR analysis demonstrated that CA formation could modulate specific immunophenotypic expressions, highlighting a complex bidirectional interaction between CA pathology and immune response. This study underscores the pivotal role of immune cells in this process through the integration of single-cell transcriptomics with MR analysis, offering a comprehensive perspective on CA pathogenesis, and potentially guiding future therapeutic strategies targeting specific immune pathways.

Indexed as

Intracranial AneurysmMendelian Randomization AnalysisMonocytesSingle-Cell AnalysisTranscriptomeGene Expression ProfilingHumansImmunophenotypingMacrophagesMuscle, Smooth, Vascularcerebral aneurysmimmune cellsMendelian randomizationpathogenesissingle-cell RNA sequencing

Identifiers

PMID38661482
PMCPMC11239559
OpenAlexW4395454687

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.