Evidence map›Paper›PMID 15632102›Full record

Trial reportAmerican journal of physiology. Endocrinology and metabolism2005

Pioglitazone improves insulin sensitivity through reduction in muscle lipid and redistribution of lipid into adipose tissue.

Neda Rasouli, Ulrika Raue, Leslie M Miles, Tong Lu, Gina B Di Gregorio, Steven C Elbein, Philip A Kern

3 registry-linked trialsAbstract readClinical TrialComparative StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in American journal of physiology. Endocrinology and metabolism, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT00108615. Cited by 64 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 2 pooled it
7.7field-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.

NCT00108615 phase4completed

Effects of Insulin Sensitizers in Subjects With Impaired Glucose Tolerance

Ran2004Enrolled48Registered outcomes2Posted comparisons0ConditionsDiabetes, Glucose Metabolism DisordersArmsCT scans, Metformin, Oral glucose tolerance test, Pioglitazone
Open the trial in the graph
NCT01589445 phase4completedstarted 2008, after this paper: background citation

Modulation of Insulin Secretion and Insulin Sensitivity in Bangladeshi Type 2 Diabetic Subjects by an Insulin Sensitizer Pioglitazone and T2DM Association With PPARG Gene Polymorphism.

Ran2008Enrolled77Registered outcomes6Posted comparisons11ConditionsType 2 Diabetes MellitusArmsMetformin hydrochloride, pioglitazone hydrochloride
Open the trial in the graph
NCT01156597 phase3completednot on this mapstarted 2008, after this paper: background citation

Effects of Pioglitazone on Reverse Cholesterol Transport and HDL Function in Persons With Diabetes

TypeinterventionalSponsorUniversity of MiamiRan2008 to 2010Enrolled30ConditionsType 2 Diabetes MellitusArmspioglitazone
3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 2 syntheses or guidelines pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. Treating prediabetes with metformin: systematic review and meta-analysis.Canadian family physician Medecin de famille canadien · 2009
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Resistance training and pioglitazone lead to improvements in muscle power during voluntary weight loss in older adults.The journals of gerontology. Series A, Biological sciences and medical sciences · 2013
    Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Trial
  15. Review
  16. Review
  17. Article
  18. Distinct Adipocyte Responses to ΔInternational journal of molecular sciences · 2025
    Article
  19. Review
  20. Review

4 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

7 authors at 2 institutions in 1 country.

Neda RasouliThe Central Arkansas Veterans Healthcare System, Department of Medicine, Division of Endocrinology, University of Arkansas for Medical Sciences, 111J LR, 4300 West 7th St., Little Rock, AR 72205, USA. Rasoulineda@UAMS.edu
Ulrika Raue
Leslie M Miles
Tong Lu
Gina B Di Gregorio
Steven C Elbein
Philip A Kern
Central Arkansas Veterans Healthcare System · USUniversity of Arkansas for Medical Sciences · US

Funding

Verruca Vulgaris--Skin Test &Candida /Mumps AntigenM01RR014288 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI PONNAPPAN, USHA · 1999 to 2006
$11.1M
Regulation of lipoprotein lipase in adipocytesR37DK039176 · NIDDK · UNIV OF ARKANSAS FOR MED SCIS · PI KERN, PHILIP A · 2006 to 2011
$1.8M
REGULATION OF LIPOPROTEIN LIPASE IN HUMAN ADIPOCYTESR01DK039176 · NIDDK · UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK · PI KERN, PHILIP A · 1993 to 2005
$1.6M
REGULATION OF LIPOPROTEIN LIPASE IN HUMAN ADIPOCYTESR29DK039176 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI KERN, PHILIP A · 1988 to 1990
–
NCRR NIH HHS M01-RR-14288NIDDK NIH HHS DK-39176
6 · The paper itself

Abstract

Patients with insulin resistance often manifest increased intramyocellular lipid (IMCL) along with increased visceral adipose tissue. This study was designed to determine whether the insulin sensitizer drugs pioglitazone and metformin would improve glucose intolerance and insulin sensitivity by decreasing IMCL. In this study, 23 generally healthy subjects with impaired glucose tolerance were randomized to receive either pioglitazone 45 mg/day or metformin 2,000 mg/day for 10 wk. Before and after treatment, we measured insulin sensitivity and abdominal subcutaneous and visceral adipose tissue with CT scanning. In addition, muscle biopsies were performed for measurement of IMCL and muscle oxidative enzymes. After treatment with pioglitazone, 2-h glucose fell from 9.6 mmol/l (172 mg/dl) to 6.1 mmol/l (119 mg/dl), whereas there was no change in 2-h glucose with metformin. With pioglitazone treatment, there was a 65% increase in insulin sensitivity along with a 34% decrease in IMCL (both P < or = 0.002). This decrease in IMCL was not due to increased muscle lipid oxidation, as there were no changes in muscle lipid oxidative enzymes. However, pioglitazone resulted in a 2.6-kg weight gain along with a significant decrease in the visceral-to-subcutaneous adipose tissue ratio. In contrast, metformin treatment resulted in no change in insulin sensitivity, IMCL, oxidative enzymes, or adipose tissue volumes. Pioglitazone improved glucose tolerance and insulin sensitivity by reducing IMCL. This reduction in IMCL was not due to an increase in muscle lipid oxidation but to a diversion of lipid from ectopic sites into subcutaneous adipose tissue.

Indexed as

Lipid MetabolismAdipose TissueAdultAgedGlucose IntoleranceHumansHypoglycemic AgentsInsulin ResistanceMetforminMiddle AgedMusclesPioglitazoneThiazolidinedionesTissue DistributionHypoglycemic AgentsMetforminPioglitazoneThiazolidinediones

Identifiers

PMID15632102
OpenAlexW2136387838

What OpenQuestion 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 OpenQuestion graph.