Evidence map›Paper›PMID 24913061›Full record

ReviewNature reviews. Cardiology2014

PET imaging of inflammation in atherosclerosis.

Jason M Tarkin, Francis R Joshi, James H F Rudd

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cardiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 218 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
218citing papers in PubMed, 2 pooled it
23.9field-weighted citation impact, top 1% 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

218 citing papers in PubMed, 2 syntheses or guidelines pooled it, 377 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Detection of Atherosclerotic Inflammation byJournal of the American College of Cardiology · 2017 · on this map
    Trial
  5. Trial
  6. Trial
  7. PET imaging of atherosclerotic plaques using the stabilin-2-targeted tracerEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
  8. Delayed total-body [European journal of nuclear medicine and molecular imaging · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. [EJNMMI research · 2026
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article

158 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Jason M TarkinDivision of Cardiovascular Medicine, University of Cambridge, Box 110, Addenbrooke's Centre for Cardiovascular Investigation, Hills Road, Cambridge CB2 2QQ, UK.
Francis R JoshiDivision of Cardiovascular Medicine, University of Cambridge, Box 110, Addenbrooke's Centre for Cardiovascular Investigation, Hills Road, Cambridge CB2 2QQ, UK.
James H F RuddDivision of Cardiovascular Medicine, University of Cambridge, Box 110, Addenbrooke's Centre for Cardiovascular Investigation, Hills Road, Cambridge CB2 2QQ, UK.
Addenbrooke's Hospital · GB

Funding

British Heart Foundation FS/12/29/29463British Heart Foundation PG/09/083/27667
6 · The paper itself

Abstract

PET imaging of atherosclerosis can quantify several in vivo pathological processes occurring within the arterial system. (18)F-fluorodeoxyglucose (FDG) is the most-commonly used PET tracer, with well-established roles in atherosclerosis imaging. In this context, the (18)F-FDG signal largely reflects tracer uptake by plaque macrophages and, therefore, inflammation with smaller contributions from other resident cell types. As a marker of plaque vulnerability, the (18)F-FDG PET signal can be used to help to identify patients at the highest risk of clinical events. (18)F-FDG PET has also been used successfully as a surrogate end point in clinical trials of antiatherosclerotic therapies. Nonetheless, imaging atherosclerosis with (18)F-FDG has several limitations. Most importantly, coronary artery imaging is problematic because (18)F-FDG accumulates in all cells that metabolize glucose, and background myocardial uptake is generally greater than any signal originating from a plaque. To help to overcome these limitations, several novel PET tracers, which might be more-specifically targeted than (18)F-FDG, have been tested in atherosclerosis imaging. These tracers are designed to track inflammation, hypoxia, neoangiogenesis, or active calcification, which are all precursors to plaque rupture and its clinical sequelae.

Indexed as

Positron-Emission TomographyRadiopharmaceuticalsAtherosclerosisFluorodeoxyglucose F18HumansInflammationMacrophagesPlaque, AtheroscleroticFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID24913061
OpenAlexW2083416749

What OpenQuestion holds

Textmetadata
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.