Evidence map›Paper›PMID 31114582›Full record

ReviewFrontiers in immunology2019

Annexin-A1: Therapeutic Potential in Microvascular Disease.

Gareth S D Purvis, Egle Solito, Christoph Thiemermann

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 108 citations in OpenAlex.

  1. Trial
  2. Screening for candidate genes and cell populations associated with atherosclerotic calcification using single-cell RNA sequencing.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  3. Annexin A1: The dawn of ischemic stroke (Review).Molecular medicine reports · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. TheFrontiers in immunology · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. BetaBiomedicines · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 3 institutions in 1 country.

Gareth S D PurvisWilliam Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Egle SolitoWilliam Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Christoph ThiemermannWilliam Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Queen Mary University of London · GBUniversity of Oxford · GBWilliam Harvey Research Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Annexin-A1 (ANXA1) was first discovered in the early 1980's as a protein, which mediates (some of the) anti-inflammatory effects of glucocorticoids. Subsequently, the role of ANXA1 in inflammation has been extensively studied. The biology of ANXA1 is complex and it has many different roles in both health and disease. Its effects as a potent endogenous anti-inflammatory mediator are well-described in both acute and chronic inflammation and its role in activating the pro-resolution phase receptor, FPR2, has been described and is now being exploited for therapeutic benefit. In the present mini review, we will endeavor to give an overview of ANXA1 biology in relation to inflammation and functions that mediate pro-resolution that are independent of glucocorticoid induction. We will focus on the role of ANXA1 in diseases with a large inflammatory component focusing on diabetes and microvascular disease. Finally, we will explore the possibility of exploiting ANXA1 as a novel therapeutic target in diabetes and the treatment of microvascular disease.

Indexed as

Addison DiseaseAnimalsAnnexin A1Cushing SyndromeDiabetes MellitusGlucocorticoidsHumansInflammationReceptors, Formyl PeptideReceptors, LipoxinVascular DiseasesAnnexin A1ANXA1 protein, humanFPR2 protein, humanGlucocorticoidsReceptors, Formyl PeptideReceptors, LipoxinAnnexin-A1 (ANXA1)diabetesinflammationsignalingtissue protection

Identifiers

PMID31114582
PMCPMC6502989
OpenAlexW2942546139

What OpenQuestion holds

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LicenceCC BY
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.