Evidence map›Paper›PMID 23804561›Full record

ArticleGut2014

An increase in the Akkermansia spp. population induced by metformin treatment improves glucose homeostasis in diet-induced obese mice.

Na-Ri Shin, June-Chul Lee, Hae-Youn Lee, Min-Soo Kim, Tae Woong Whon, Myung-Shik Lee, Jin-Woo Bae

Registry-linked trialAbstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Gut, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03629639 (Metformin for Treatment of Psoriasis Combined With Disorders of Glucose and Lipid Metabolism), which is not on this map. Cited by 851 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
851citing papers in PubMed, 4 pooled it
31.1field-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.

NCT03629639 phase4unknown statusnot on this mapstarted 2018, after this paper: background citation

Metformin for Treatment of Psoriasis Combined With Disorders of Glucose and Lipid Metabolism: A Double-Blind, Randomized, Placebo-Controlled Study

TypeinterventionalSponsorCentral South UniversityRan2018 to 2020Enrolled80ConditionsPsoriasis Vulgaris With Metabolic DisordersArmsMetformin
3 · Its place in the literature

Who cites it

851 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,535 citations in OpenAlex.

  1. Pooled it
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  3. Nutrients · 2024
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  11. Gut microbes · 2026
    Article
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791 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Na-Ri ShinDepartment of Life and Nanopharmaceutical Sciences and Department of Biology, Kyung Hee University, , Seoul, Korea.
June-Chul Lee
Hae-Youn Lee
Min-Soo Kim
Tae Woong Whon
Myung-Shik Lee
Jin-Woo Bae
Kyung Hee University · KRSungkyunkwan University · KRSamsung Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent evidence indicates that the composition of the gut microbiota contributes to the development of metabolic disorders by affecting the physiology and metabolism of the host. Metformin is one of the most widely prescribed type 2 diabetes (T2D) therapeutic agents.

objectiveTo determine whether the antidiabetic effect of metformin is related to alterations of intestinal microbial composition.

designC57BL/6 mice, fed either a normal-chow diet or a high-fat diet (HFD), were treated with metformin for 6 weeks. The effect of metformin on the composition of the gut microbiota was assessed by analysing 16S rRNA gene sequences with 454 pyrosequencing. Adipose tissue inflammation was examined by flow cytometric analysis of the immune cells present in visceral adipose tissue (VAT).

resultsMetformin treatment significantly improved the glycaemic profile of HFD-fed mice. HFD-fed mice treated with metformin showed a higher abundance of the mucin-degrading bacterium Akkermansia than HFD-fed control mice. In addition, the number of mucin-producing goblet cells was significantly increased by metformin treatment (p<0.0001). Oral administration of Akkermansia muciniphila to HFD-fed mice without metformin significantly enhanced glucose tolerance and attenuated adipose tissue inflammation by inducing Foxp3 regulatory T cells (Tregs) in the VAT.

conclusionsModulation of the gut microbiota (by an increase in the Akkermansia spp. population) may contribute to the antidiabetic effects of metformin, thereby providing a new mechanism for the therapeutic effect of metformin in patients with T2D. This suggests that pharmacological manipulation of the gut microbiota in favour of Akkermansia may be a potential treatment for T2D.

Indexed as

AnimalsBiomarkersBlood GlucoseDiet, High-FatDrug Administration ScheduleFlow CytometryHomeostasisHypoglycemic AgentsInflammationIntestinesIntra-Abdominal FatMetforminMiceMice, Inbred C57BLMice, ObeseMicrobiotaBiomarkersBlood GlucoseHypoglycemic AgentsMetforminIntestinal BacteriaMucinsObesityPharmacotherapy

Identifiers

PMID23804561
OpenAlexW2139334262

What OpenQuestion holds

Textmetadata
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.