Evidence mapPaperPMID 17914032Full record

Trial reportDiabetes2008

Comparison of the effects of pioglitazone and metformin on hepatic and extra-hepatic insulin action in people with type 2 diabetes.

Rita Basu, Pankaj Shah, Ananda Basu, Barbara Norby, Betty Dicke, Visvanathan Chandramouli, Ohad Cohen, Bernard R Landau, Robert A Rizza

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Diabetes, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04271189 (A Prospective, Randomized, Parallel-group, Adaptive Design Phase IIb/III, Multicenter Study, to Assess the Efficacy of Polychemotherapy for Inducing Remission of Newly Diagnosed Type 2 Diabetes.), which is not on this map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 9% 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.

NCT04271189 phase3completedstarted 2020, after this paper: background citation

A Prospective, Randomized, Parallel-group, Adaptive Design Phase IIb/III, Multicenter Study, to Assess the Efficacy of Polychemotherapy for Inducing Remission of Newly Diagnosed Type 2 Diabetes.

Ran2020Enrolled108Registered outcomes10Posted comparisons0ConditionsNewly Diagnosed Type 2 DiabetesArmsMetformin-Sitagliptin-Empaglifozin-Pioglitazone, Standard of care
Open the trial in the graph
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Risk of fatal and nonfatal lactic acidosis with metformin use in type 2 diabetes mellitus.The Cochrane database of systematic reviews · 2010 · on this map
    Pooled it
  4. Trial
  5. Pioglitazone after Ischemic Stroke or Transient Ischemic Attack.The New England journal of medicine · 2016 · on this map
    Trial
  6. Trial
  7. Trial
  8. Article
  9. Review
  10. Targeting Adrenergic Receptors in Metabolic Therapies for Heart Failure.International journal of molecular sciences · 2021
    Review
  11. Observational
  12. Review
  13. The Eeffect of Metformin Combined with Calcium-Vitamin DAdvanced pharmaceutical bulletin · 2018
    Article
  14. Article
  15. Review
  16. Combining metformin therapy with caloric restriction for the management of type 2 diabetes and nonalcoholic fatty liver disease in obese rats.Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme · 2015
    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

9 authors at 5 institutions in 2 countries.

Rita BasuDivision of Endocrinology, Diabetes, Metabolism, and Nutrition, Mayo Clinic, 200 1st St. SW, Room 5-194 Joseph, Rochester, MN 55905, USA.
Pankaj Shah
Ananda Basu
Barbara Norby
Betty Dicke
Visvanathan Chandramouli
Ohad Cohen
Bernard R Landau
Robert A Rizza
Mayo Clinic · USCase Western Reserve University · USSheba Medical Center · ILThe University of Texas MD Anderson Cancer Center · USUniversity School · US

Funding

ZESTRIL VS. VERAPAMIL IN THE TREATMENT OF HYPERTENSIONM01RR000585 · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · 1985 to 2005
$26.6M
Carbohydrate Metabolic PathwaysR01DK014507 · CASE WESTERN RESERVE UNIVERSITY · 1986 to 2005
$2.5M
MECHANISMS OF INSULIN RESISTANCE in ManR37DK029953 · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · 1996 to 2003
$1.8M
MECHANISMS OF INSULIN RESISTANCE IN MANR01DK029953 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RITA BASU · 1986 to 2024
$1.6M
CARBOHYDRATE AND LIPID METABOLIC PATHWAYSR37DK014507 · CASE WESTERN RESERVE UNIVERSITY · 1988 to 1995
NCRR NIH HHS RR-00585NCRR NIH HHS U 54RR-24150-1NIDDK NIH HHS DK-14507NIDDK NIH HHS DK-29953
6 · The paper itself

Abstract

objectiveTo determine mechanisms by which pioglitazone and metformin effect hepatic and extra-hepatic insulin action. RESEARCH DESIGN AND

methodsThirty-one subjects with type 2 diabetes were randomly assigned to pioglitazone (45 mg) or metformin (2,000 mg) for 4 months.

resultsGlucose was clamped before and after therapy at approximately 5 mmol/l, insulin raised to approximately 180 pmol/l, C-peptide suppressed with somatostatin, glucagon replaced at approximately 75 pg/ml, and glycerol maintained at approximately 200 mmol/l to ensure comparable and equal portal concentrations on all occasions. Insulin-induced stimulation of glucose disappearance did not differ before and after treatment with either pioglitazone (23 +/- 3 vs. 24 +/- 2 micromol x kg(-1) x min(-1)) or metformin (22 +/- 2 vs. 24 +/- 3 micromol x kg(-1) x min(-1)). In contrast, pioglitazone enhanced (P < 0.01) insulin-induced suppression of both glucose production (6.0 +/- 1.0 vs. 0.2 +/- 1.6 micromol x kg(-1) x min(-1)) and gluconeogenesis (n = 11; 4.5 +/- 0.9 vs. 0.8 +/- 1.2 micromol x kg(-1) x min(-1)). Metformin did not alter either suppression of glucose production (5.8 +/- 1.0 vs. 5.0 +/- 0.8 micromol x kg(-1) x min(-1)) or gluconeogenesis (n = 9; 3.7 +/- 0.8 vs. 2.6 +/- 0.7 micromol x kg(-1) x min(-1)). Insulin-induced suppression of free fatty acids was greater (P < 0.05) after treatment with pioglitazone (0.14 +/- 0.03 vs. 0.06 +/- 0.01 mmol/l) but unchanged with metformin (0.12 +/- 0.03 vs. 0.15 +/- 0.07 mmol/l).

conclusionsThus, relative to metformin, pioglitazone improves hepatic insulin action in people with type 2 diabetes, partly by enhancing insulin-induced suppression of gluconeogenesis. On the other hand, both drugs have comparable effects on insulin-induced stimulation of glucose uptake.

Indexed as

Blood GlucoseBody Mass IndexC-PeptideDiabetes Mellitus, Type 2Diet, DiabeticDouble-Blind MethodDrug Administration ScheduleFatty Acids, NonesterifiedFemaleGlucagonGluconeogenesisGlucose Clamp TechniqueGlycerolGlycogenolysisHumansHypoglycemic AgentsBlood GlucoseC-PeptideFatty Acids, NonesterifiedGlucagonGlycerolHypoglycemic AgentsInsulinMetforminPioglitazonePlacebosThiazolidinediones

Identifiers

PMID17914032
OpenAlexW2156803989

What Socratic holds

Texttitle and abstract
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.