SynthesisCurrent atherosclerosis reports2025
Review of OxLDL Driven Inflammatory Cell Activation.
Synthesis in Current atherosclerosis reports, 2025. 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.
- Lipid Metabolism Modulation by a Flavonoid-StandardizedJournal of experimental pharmacology · 2026Trial
- Progress in the Cross-Organ Biomarker oxLDL in Promoting Pathological Neovascular Diseases.Antioxidants (Basel, Switzerland) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purpose of reviewAtherosclerosis is considered to be an inflammatory disease due to the presence of macrophages and T-cells within the artery plaques. Atherosclerotic plaques contain significant levels of oxidised low density lipoprotein (oxLDL) suggesting it is a source of the observed inflammation. In this systematic review, the PubMed, Medline and Scopus databases were searched for studies on the inflammatory effects of oxLDL and therapeutic treatments intended to prevent inflammation in humans or human-derived cell lines. RECENT
findingsOut of the 65 articles that passed through a full-text examination of the inflammatory effects of oxLDL, eight were considered suitable for inclusion in the study. Fifty studies out of 75 studies which were subjected to full-text review of anti-inflammatory agents were selected. Three out of 4 studies that measured the effect of oxLDL stimulation on interleukin (IL)-1β reported significant increase in IL-1β level, while 4 out of 6 studies that measured IL-6 reported significant increase in IL-6 level. Four out of 6 studies that measured tumour necrosis factor (TNF)-α reported significant increase in TNF-α after oxLDL stimulation, while 2 studies reported significant increase in caspase-1 activation by oxLDL. Although some of the studies on the anti-inflammatory agents demonstrated significant inhibition of inflammation, none of the anti-inflammatory agents directly targeted oxLDL immune activation. It is evident that there is an interplay between cholesterol and vascular cells in the pathogenesis of atherosclerosis, but there is a gap between the suggested effects of oxLDL in literatures and actual intrinsic effects of oxLDL on the vascular cells.
Indexed as
Identifiers
41193878What OpenQuestion holds
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 OpenQuestion graph.