Evidence mapPaperPMID 35909294Full record

ReviewCurrent medicinal chemistry2023

Repurposing Metformin for Vascular Disease.

Chris R Triggle, Isra Marei, Kevin Ye, Hong Ding, Todd J Anderson, Morley D Hollenberg, Michael A Hill

Open access · hybridAbstract readReview
In one paragraph

Review in Current medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Journal of pharmacopuncture · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Advances in the Insulin-Heart Axis: Current Therapies and Future Directions.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
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

7 authors at 4 institutions in 3 countries.

Chris R TriggleDepartment of Pharmacology & Medical Education, Weill Cornell Medicine in Qatar, PO Box 24144, Education City, Doha, Qatar.
Isra MareiDepartment of Pharmacology & Medical Education, Weill Cornell Medicine in Qatar, PO Box 24144, Education City, Doha, Qatar.
Kevin YeDepartment of Biomedical Physiology & Kinesiology, Simon Fraser University, Burnaby, British Columbia, Canada, V5A 1S6.
Hong DingDepartment of Pharmacology & Medical Education, Weill Cornell Medicine in Qatar, PO Box 24144, Education City, Doha, Qatar.
Todd J AndersonDepartment of Cardiac Sciences and Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada, T2N 4N1.
Morley D HollenbergDepartment of Physiology & Pharmacology, and Department of Medicine, Cumming School of Medicine, University of Calgary, Canada, T2N 4N1.
Michael A HillDalton Cardiovascular Research Center & Department of Medical Pharmacology & Physiology, School of Medicine, University of Missouri, Columbia 65211, Missouri, USA.
Weill Cornell Medical College in Qatar · QAUniversity of Calgary · CASimon Fraser University · CAUniversity of Missouri · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metformin has been used as an oral anti-hyperglycaemic drug since the late 1950s; however, following the release in 1998 of the findings of the 20-year United Kingdom Prospective Diabetes Study (UKPDS), metformin use rapidly increased and today is the first-choice anti-hyperglycaemic drug for patients with type 2 diabetes (T2D). Metformin is in daily use by an estimated 150 million people worldwide. Historically, the benefits of metformin as an anti-diabetic and cardiovascular-protective drug have been linked to effects in the liver, where it acts to inhibit gluconeogenesis and lipogenesis, as well as reduce insulin resistance and enhance peripheral glucose utilization. However, direct protective effects on the endothelium and effects in the gut prior to metformin absorption are now recognized as important. In the gut, metformin modulates the glucagon-like peptide- 1 (GLP-1) - gut-brain axis and impacts the intestinal microbiota. As the apparent number of putative tissue and cellular targets for metformin has increased, so has the interest in re-purposing metformin to treat other diseases that include polycystic ovary syndrome (PCOS), cancer, neurodegenerative diseases, and COVID-19. Metformin is also being investigated as an anti-ageing drug. Of particular interest is whether metformin provides the same level of vascular protection in individuals other than those with T2D, including obese individuals with metabolic syndrome, or in the setting of vascular thromboinflammation caused by SARS-CoV-2. In this review, we critically evaluate the literature to highlight clinical settings in which metformin might be therapeutically repurposed for the prevention and treatment of vascular disease.

Indexed as

Drug RepositioningVascular DiseasesAgingAnimalsCOVID-19Endothelial CellsExerciseHumansMetforminMetforminCOVID-19endotheliuminflammationMetforminobesitySARS-CoV-2type 2 diabetesvascular disease

Identifiers

PMID35909294
PMCPMC10286558
OpenAlexW4289135221

What Socratic holds

Textmetadata
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 Socratic graph.