ReviewFrontiers in cardiovascular medicine2026
Emerging insights into inflammation-driven atherosclerosis: immune cell mechanisms.
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.
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.
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.
Who cites it
2 citing papers in PubMed.
- Exercise in Patients with Subclinical Atherosclerosis: Mechanisms, Clinical Evidence, and Practical Recommendations.Current atherosclerosis reports · 2026Review
- Antioxidants in Cardiovascular Medicine: Emerging Trends and Future Perspectives.Antioxidants (Basel, Switzerland) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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Registered trials
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.