Evidence map›Paper›PMID 32333835›Full record

ReviewCell metabolism2020

Benefits of Metformin in Attenuating the Hallmarks of Aging.

Ameya S Kulkarni, Sriram Gubbi, Nir Barzilai

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Cell metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06459310 (A Phase II Exploratory Clinical Study Investigating the Geroprotective Effect of Metformin in Middle-aged and Elderly People), which is not on this map. Cited by 425 papers.

0numbers the graph read from it
0cells of the map it votes in
425citing papers in PubMed
31.8field-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.

NCT06459310 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

A Phase II Exploratory Clinical Study Investigating the Geroprotective Effect of Metformin in Middle-aged and Elderly People

TypeinterventionalSponsorXuanwu Hospital, BeijingRan2024 to 2028Enrolled130ConditionsMetformin, AgingArmsMetformin Hydrochloride tablet, Placebo
3 · Its place in the literature

Who cites it

425 citing papers in PubMed, 692 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Review
  5. Article
  6. Article
  7. Review
  8. Evolutionary genetics of ageing.Nature reviews. Genetics · 2026
    Review
  9. Review
  10. Review
  11. AAV-mediated FGF21 gene therapy promotes health span extension by whole-body tissue-specific adaptations.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

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

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 2 institutions in 1 country.

Ameya S KulkarniInstitute for Aging Research, Albert Einstein College of Medicine, Bronx, New York, NY, USA; Department of Medicine, Division of Endocrinology, Albert Einstein College of Medicine, Bronx, New York, NY, USA. Electronic address: ameyak225@gmail.com.
Sriram GubbiMetabolic Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Nir BarzilaiInstitute for Aging Research, Albert Einstein College of Medicine, Bronx, New York, NY, USA; Department of Medicine, Division of Endocrinology, Albert Einstein College of Medicine, Bronx, New York, NY, USA. Electronic address: nir.barzilai@einsteinmed.org.
Albert Einstein College of Medicine · USNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI JEFFREY E. PESSIN · 2015 to 2026
$27.7M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BARZILAI, NIR J · 2010 to 2024
$10.8M
ROLE OF NUTRIENTS IN AGE-RELATED INSULIN RESISTANCEP01AG021654 · NIA · YESHIVA UNIVERSITY · PI BARZILAI, NIR J · 2003 to 2007
$10.6M
NIA NIH HHS P01 AG021654NIA NIH HHS P30 AG038072NIDDK NIH HHS P30 DK020541
6 · The paper itself

Abstract

Biological aging involves an interplay of conserved and targetable molecular mechanisms, summarized as the hallmarks of aging. Metformin, a biguanide that combats age-related disorders and improves health span, is the first drug to be tested for its age-targeting effects in the large clinical trial-TAME (targeting aging by metformin). This review focuses on metformin's mechanisms in attenuating hallmarks of aging and their interconnectivity, by improving nutrient sensing, enhancing autophagy and intercellular communication, protecting against macromolecular damage, delaying stem cell aging, modulating mitochondrial function, regulating transcription, and lowering telomere attrition and senescence. These characteristics make metformin an attractive gerotherapeutic to translate to human trials.

Indexed as

AgingAnimalsAutophagyCell CommunicationCellular SenescenceHumansHypoglycemic AgentsMetforminMitochondriaHypoglycemic AgentsMetforminagingaging hallmarkshealth spanlongevitymetabolismmetforminTAME

Identifiers

PMID32333835
PMCPMC7347426
OpenAlexW3019800544

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.