Evidence mapPaperPMID 27465265Full record

Trial reportDiabetes care2016

Pioglitazone Prevents Diabetes in Patients With Insulin Resistance and Cerebrovascular Disease.

Silvio E Inzucchi, Catherine M Viscoli, Lawrence H Young, Karen L Furie, Mark Gorman, Anne M Lovejoy, Samuel Dagogo-Jack, Faramarz Ismail-Beigi, Mary T Korytkowski, Richard E Pratley and 3 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes care, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 4 pooled it
6.9field-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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 4 syntheses or guidelines pooled it, 80 citations in OpenAlex.

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  7. Lipid metabolism in homeostasis and disease.Signal transduction and targeted therapy · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 1 country.

Silvio E InzucchiYale School of Medicine, New Haven, CT silvio.inzucchi@yale.edu.
Catherine M ViscoliYale School of Medicine, New Haven, CT.
Lawrence H YoungYale School of Medicine, New Haven, CT.
Karen L FurieAlpert Medical School of Brown University, Providence, RI.
Mark GormanVermont College of Medicine, Burlington, VT.
Anne M LovejoyYale School of Medicine, New Haven, CT.
Samuel Dagogo-JackUniversity of Tennessee Health Science Center, Memphis, TN.
Faramarz Ismail-BeigiCase Western Reserve University and VA Medical Center, Cleveland, OH.
Mary T KorytkowskiUniversity of Pittsburgh School of Medicine, Pittsburgh, PA.
Richard E PratleyFlorida Hospital, Orlando, FL.
Gregory G SchwartzVA Medical Center and University of Colorado School of Medicine, Denver, CO.
Walter N KernanYale School of Medicine, New Haven, CT.
IRIS Trial Investigators
Yale University · USAdventHealth Orlando · USBrown University · USCase Western Reserve University · USDenver VA Medical Center · USUniversity of Pittsburgh · USUniversity of Tennessee Health Science Center · USUniversity of Vermont · US

Funding

Insulin Resistance Intervention after Stroke TrialU01NS044876 · YALE UNIVERSITY · 2004 to 2005
$12.9M
Yale Diabetes Research CenterP30DK045735 · YALE UNIVERSITY · 1993 to 2025
$10.2M
Yale Clinical and Translational Science AwardUL1TR001863 · YALE UNIVERSITY · 2025 to 2025
$9.9M
NCATS NIH HHS UL1 TR001863NIDDK NIH HHS P30 DK045735NINDS NIH HHS U01 NS044876
6 · The paper itself

Abstract

objectiveThe Insulin Resistance Intervention after Stroke (IRIS) trial recently found that pioglitazone reduced risk for stroke and myocardial infarction in patients with insulin resistance but without diabetes who had had a recent ischemic stroke or transient ischemic attack (TIA). This report provides detailed results on the metabolic effects of pioglitazone and the trial's prespecified secondary aim of diabetes prevention. RESEARCH DESIGN AND

methodsA total of 3,876 patients with recent ischemic stroke or TIA, no history of diabetes, fasting plasma glucose (FPG) <126 mg/dL, and insulin resistance by homeostasis model assessment of insulin resistance (HOMA-IR) score >3.0 were randomly assigned to pioglitazone or placebo. Surveillance for diabetes onset during the trial was accomplished by periodic interviews and annual FPG testing.

resultsAt baseline, the mean FPG, HbA1c, insulin, and HOMA-IR were 98.2 mg/dL (5.46 mmol/L), 5.8% (40 mmol/mol), 22.4 μIU/mL, and 5.4, respectively. After 1 year, mean HOMA-IR and FPG decreased to 4.1 and 95.1 mg/dL (5.28 mmol/L) in the pioglitazone group and rose to 5.7 and 99.7 mg/dL (5.54 mmol/L), in the placebo group (all P < 0.0001). Over a median follow-up of 4.8 years, diabetes developed in 73 (3.8%) participants assigned to pioglitazone compared with 149 (7.7%) assigned to placebo (hazard ratio [HR] 0.48 [95% CI 0.33-0.69]; P < 0.0001). This effect was predominately driven by those with initial impaired fasting glucose (FPG >100 mg/dL [5.6 mmol/L]; HR 0.41 [95% CI 0.30-0.57]) or elevated HbA1c (>5.7% [39 mmol/mol]; HR 0.46 [0.34-0.62]).

conclusionsAmong patients with insulin resistance but without diabetes who had had a recent ischemic stroke or TIA, pioglitazone decreased the risk of diabetes while also reducing the risk of subsequent ischemic events. Pioglitazone is the first medication shown to prevent both progression to diabetes and major cardiovascular events as prespecified outcomes in a single trial.

Indexed as

Ischemic Attack, TransientAgedBlood GlucoseDiabetes MellitusDiabetes Mellitus, Type 2FemaleHumansHypoglycemic AgentsInsulin ResistanceMaleMiddle AgedMyocardial InfarctionPioglitazoneStrokeThiazolidinedionesBlood GlucoseHypoglycemic AgentsPioglitazoneThiazolidinediones

Identifiers

PMID27465265
PMCPMC5033078
OpenAlexW2522865695

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.