ReviewCurrent opinion in lipidology2025
Genetic influences on macrophage function and lipid uptake in atherosclerosis.
Review in Current opinion in lipidology, 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.
- Integrative Single-Cell Transcriptomics, Multi-Omics Analyses, and Computational Pharmacology Reveal Macrophage Heterogeneity and the Putative THBS1-CD36 Axis in Coronary Atherosclerosis.Chemical biology & drug design · 2026Article
- Metabolic regulation of macrophage polarization in myocardial infarction: from mechanisms to targeted therapies.Journal of translational medicine · 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
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purpose of reviewMacrophages can accumulate lipid droplets in their cytoplasm resulting in the foamy appearance seen in various diseases, especially atherosclerosis. This review assesses new insights from single cell analyses into the role of different human macrophage subpopulations and genetic risk in atherosclerotic disease. RECENT
findingsSingle cell transcriptomic studies have identified TREM2hi foamy macrophages as a key population in both human and mouse atherosclerotic plaques. In addition, a TREM1hi/PLIN2hi population in human plaques has pro-inflammatory properties. Combined single cell transcriptomic and epigenetic multiomic profiling identified a population of CD52hi lipid-handling macrophages that are enriched for heritability of atherosclerotic disease. Molecular mechanisms have been identified linking gene-regulatory effects of disease-associated polymorphisms to the macrophage response to ox-LDL. SUMMARY: Recent studies have used singe cell approaches to provide new insights into macrophage subsets, their interactions with lipid species and their role in mediating genetic influences on disease risk.
Indexed as
Identifiers
What 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.