Evidence map›Paper›PMID 23028442›Full record

ArticlePloS one2012

Metformin prevents and reverses inflammation in a non-diabetic mouse model of nonalcoholic steatohepatitis.

Yuki Kita, Toshinari Takamura, Hirofumi Misu, Tsuguhito Ota, Seiichiro Kurita, Yumie Takeshita, Masafumi Uno, Naoto Matsuzawa-Nagata, Ken-Ichiro Kato, Hitoshi Ando and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05317806 (Use of Metformin in Prevention and Treatment of Cardiac Fibrosis in PAI-1 Deficient Population), which is not on this map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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.

NCT05317806 phase4active not recruitingnot on this mapstarted 2022, after this paper: background citation

Use of Metformin in Prevention and Treatment of Cardiac Fibrosis in PAI-1 Deficient Population

TypeinterventionalSponsorIndiana Hemophilia &Thrombosis Center, Inc.Ran2022 to 2027Enrolled15ConditionsPlasminogen Activator Inhibitor-1 Deficiency, Cardiac FibrosisArmsMetformin Extended Release Oral Tablet
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  4. Article
  5. A Framework for Autonomous AI-Driven Drug Discovery.bioRxiv : the preprint server for biology · 2026
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  16. A new preclinical model of western diet-induced progression of non-alcoholic steatohepatitis to hepatocellular carcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
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  17. Review
  18. Review
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17 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

19 authors at 4 institutions in 1 country.

Yuki KitaDepartment of Disease Control and Homeostasis, Kanazawa University Graduate School of Medical Science, Ishikawa, Japan.
Toshinari Takamura
Hirofumi Misu
Tsuguhito Ota
Seiichiro Kurita
Yumie Takeshita
Masafumi Uno
Naoto Matsuzawa-Nagata
Ken-Ichiro Kato
Hitoshi Ando
Akio Fujimura
Koji Hayashi
Toru Kimura
Yinhua Ni
Toshiki Otoda
Ken-ichi Miyamoto
Yoh Zen
Yasuni Nakanuma
Shuichi Kaneko
Kanazawa University · JPKanazawa Medical University · JPJichi Medical University · JPSumitomo Dainippon Pharma (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOptimal treatment for nonalcoholic steatohepatitis (NASH) has not yet been established, particularly for individuals without diabetes. We examined the effects of metformin, commonly used to treat patients with type 2 diabetes, on liver pathology in a non-diabetic NASH mouse model. METHODOLOGY/PRINCIPAL

findingsEight-week-old C57BL/6 mice were fed a methionine- and choline-deficient plus high fat (MCD+HF) diet with or without 0.1% metformin for 8 weeks. Co-administration of metformin significantly decreased fasting plasma glucose levels, but did not affect glucose tolerance or peripheral insulin sensitivity. Metformin ameliorated MCD+HF diet-induced hepatic steatosis, inflammation, and fibrosis. Furthermore, metformin significantly reversed hepatic steatosis and inflammation when administered after the development of experimental NASH. CONCLUSIONS/SIGNIFICANCE: These histological changes were accompanied by reduced hepatic triglyceride content, suppressed hepatic stellate cell activation, and the downregulation of genes involved in fatty acid metabolism, inflammation, and fibrogenesis. Metformin prevented and reversed steatosis and inflammation of NASH in an experimental non-diabetic model without affecting peripheral insulin resistance.

Indexed as

AnimalsCluster AnalysisDisease Models, AnimalFatty LiverGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksHepatic Stellate CellsHepatitisLipid MetabolismLiver CirrhosisMetforminMiceMice, Inbred NODNon-alcoholic Fatty Liver DiseasePlasminogen Activator Inhibitor 1MetforminPlasminogen Activator Inhibitor 1

Identifiers

PMID23028442
PMCPMC3445596
OpenAlexW2126753352

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.