Evidence map›Paper›PMID 35993316›Full record

ReviewEuropean heart journal. Cardiovascular Imaging2022

Unravelling the role of macrophages in cardiovascular inflammation through imaging: a state-of-the-art review.

Reece Parry, Kamran Majeed, Fiona Pixley, Graham Scott Hillis, Roslyn Jane Francis, Carl Johann Schultz

Open access · bronzeAbstract readReview
In one paragraph

Review in European heart journal. Cardiovascular Imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. CD45-targeted PET enables the visualization of inflammatory conditions.American journal of nuclear medicine and molecular imaging · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 1 institution in 2 countries.

Reece ParrySchool of Medicine, University of Western Australia, Perth 6009, Australia.ORCID 0000-0001-6533-5870
Kamran MajeedSchool of Medicine, University of Western Australia, Perth 6009, Australia.ORCID 0000-0002-2298-3138
Fiona PixleySchool of Biomedical Sciences, Pharmacology and Toxicology, University of Western Australia, Perth 6009, Australia.ORCID 0000-0002-1571-2532
Graham Scott HillisSchool of Medicine, University of Western Australia, Perth 6009, Australia.ORCID 0000-0003-2417-4673
Roslyn Jane FrancisSchool of Medicine, University of Western Australia, Perth 6009, Australia.ORCID 0000-0002-6256-1351
Carl Johann SchultzSchool of Medicine, University of Western Australia, Perth 6009, Australia.ORCID 0000-0002-0847-4361
The University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease remains the leading cause of death and disability for patients across the world. Our understanding of atherosclerosis as a primary cholesterol issue has diversified, with a significant dysregulated inflammatory component that largely remains untreated and continues to drive persistent cardiovascular risk. Macrophages are central to atherosclerotic inflammation, and they exist along a functional spectrum between pro-inflammatory and anti-inflammatory extremes. Recent clinical trials have demonstrated a reduction in major cardiovascular events with some, but not all, anti-inflammatory therapies. The recent addition of colchicine to societal guidelines for the prevention of recurrent cardiovascular events in high-risk patients with chronic coronary syndromes highlights the real-world utility of this class of therapies. A highly targeted approach to modification of interleukin-1-dependent pathways shows promise with several novel agents in development, although excessive immunosuppression and resulting serious infection have proven a barrier to implementation into clinical practice. Current risk stratification tools to identify high-risk patients for secondary prevention are either inadequately robust or prohibitively expensive and invasive. A non-invasive and relatively inexpensive method to identify patients who will benefit most from novel anti-inflammatory therapies is required, a role likely to be fulfilled by functional imaging methods. This review article outlines our current understanding of the inflammatory biology of atherosclerosis, upcoming therapies and recent landmark clinical trials, imaging modalities (both invasive and non-invasive) and the current landscape surrounding functional imaging including through targeted nuclear and nanobody tracer development and their application.

Indexed as

AtherosclerosisCardiovascular DiseasesCoronary Artery DiseaseAnti-Inflammatory AgentsHumansInflammationMacrophagesAnti-Inflammatory Agents68Gallium-DOTATATE positron emission tomographyactivated macrophagescardiovascular inflammationcoronary artery diseasecoronary imagingoptical coherence tomography

Identifiers

PMID35993316
PMCPMC9671294
OpenAlexW4292582388

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.