Evidence map›Paper›PMID 42465528›Full record

ReviewFrontiers in cardiovascular medicine2026

Emerging insights into inflammation-driven atherosclerosis: immune cell mechanisms.

Abdullahi Osman Mohamud, Zhiyin Dai

Abstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Abdullahi Osman MohamudDepartment of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, China.
Zhiyin DaiDepartment of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis is a chronic inflammatory disease marked by the deposition of lipids, fibrous components, and calcification in the major arteries. The process is initiated by endothelial activation, which increases vascular permeability, promotes leukocyte adhesion, and leads to the migration of inflammatory cells into the arterial wall. These events trigger vascular constriction and activate inflammatory pathways, together promoting atheromatous plaque development. This review integrates emerging concepts in the immune cascade, detailing how recruited immune cells such as macrophages, T cells, B cells, dendritic cells (DCs), and neutrophils interact to sustain inflammation within developing plaques, as revealed by single-cell omics approaches. In addition, we discuss novel ideas, such as phenotypic switching of vascular smooth muscle cells into macrophage-like foam cells and the systemic effects of clonal haematopoiesis. Finally, we explore how systemic and environmental factors, including gut microbiota, epigenetic changes, hypertension, diabetes, obesity, and smoking, maintain a state of trained immunity and meta-inflammation that exacerbates disease, thus providing a conceptual framework for targeting inflammatory axes in future therapeutic strategies.

Indexed as

atherosclerosisclonal haematopoiesisgut microbiotameta-inflammation.single-cell omicstrained immunity

Identifiers

PMID42465528
PMCPMC13373088

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.