Evidence map›Paper›PMID 39196223›Full record

ReviewNature cardiovascular research2024

Immunometabolism in atherosclerotic disorders.

Andrew J Fleetwood, Jonathan Noonan, Nicole La Gruta, Axel Kallies, Andrew J Murphy

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature cardiovascular research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Molecular Research in Cardiovascular Disease, 3rd Edition.International journal of molecular sciences · 2026
    Article
  5. Review
  6. Lactate Enhances CD8International journal of molecular sciences · 2026
    Article
  7. Review
  8. Review
  9. Frontiers in microbiology · 2026
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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

5 authors.

Andrew J FleetwoodDivision of Immunometabolism, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia. andrew.fleetwood@baker.edu.au.ORCID http://orcid.org/0000-0002-6803-3533
Jonathan NoonanDivision of Immunometabolism, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-9173-0903
Nicole La GrutaBiomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Axel KalliesThe Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia.
Andrew J MurphyDivision of Immunometabolism, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia. andrew.murphy@baker.edu.au.ORCID http://orcid.org/0000-0001-7039-7777

Funding

Department of Health | National Health and Medical Research Council (NHMRC) GNT1194329Department of Health | National Health and Medical Research Council (NHMRC) GNT2012119Department of Health | National Health and Medical Research Council (NHMRC) GNT2017335Department of Health | National Health and Medical Research Council (NHMRC) GNT202152
6 · The paper itself

Abstract

Cardiovascular diseases (CVDs), including atherosclerosis, myocardial infarction and heart failure, are the leading causes of morbidity and mortality worldwide. Emerging evidence suggests a crucial role for immune cell dysfunction and inflammation in the progression of this complex set of diseases. Recent advances demonstrate that immune cells, tightly linked to CVD pathogenesis, are sensitive to environmental signals and respond by engaging immunometabolic networks that shape their behavior. Inflammatory cues and altered nutrient availability within atherosclerotic plaques or following ischemia synergize to elicit metabolic shifts in immune cells that influence the course of disease pathology. Understanding these metabolic adaptations and how they contribute to cellular dysfunction may reveal novel therapeutic approaches for the treatment of CVD. Here we provide a comprehensive summary of the metabolic reprogramming that occurs in immune cells and their progenitors during CVD, offering insights into the potential therapeutic interventions to mitigate disease progression.

Indexed as

AtherosclerosisAnimalsEnergy MetabolismHumansInflammationPlaque, AtheroscleroticSignal Transduction

Identifiers

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.