Evidence mapPaperPMID 39084829Full record

Trial reportJournal of the American College of Cardiology2024

Liraglutide Improves Myocardial Perfusion and Energetics and Exercise Tolerance in Patients With Type 2 Diabetes.

Amrit Chowdhary, Sharmaine Thirunavukarasu, Tobin Joseph, Nicholas Jex, Sindhoora Kotha, Marilena Giannoudi, Henry Procter, Lizette Cash, Sevval Akkaya, David Broadbent and 9 more

Registry-linked trialAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American College of Cardiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT04657939. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
field-weighted citation impact
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.

NCT04657939 phase4completed

Targeting Beta-cell Failure in Lean Patients With Type 2 Diabetes

Ran2020Enrolled57Registered outcomes8Posted comparisons0ConditionsDiabetes Mellitus, Type 2Armsliraglutide, Pioglitazone
Open the trial in the graph
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  4. Cardiac energetics in health and disease: a meta-analysis.European heart journal. Imaging methods and practice · 2026
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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.

Amrit ChowdharyUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Sharmaine ThirunavukarasuUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Tobin JosephUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Nicholas JexUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Sindhoora KothaUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Marilena GiannoudiUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Henry ProcterUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Lizette CashUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Sevval AkkayaUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
David BroadbentUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Hui XueNational Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.
Peter SwobodaUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Ladislav ValkovičCentre for Clinical Magnetic Resonance Research (OCMR), RDM Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom; Institute of Measurement Science, Slovak Academy of Sciences, Bratislava, Slovakia.
Peter KellmanNational Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.
Sven PleinUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom.
Oliver J RiderCentre for Clinical Magnetic Resonance Research (OCMR), RDM Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.
Stefan NeubauerCentre for Clinical Magnetic Resonance Research (OCMR), RDM Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.
John P GreenwoodBaker Heart and Diabetes Institute, Melbourne, Australia; Monash University, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
Eylem LeveltUniversity of Leeds, Leeds Institute of Cardiovascular and Metabolic Medicine, Leeds, United Kingdom; Baker Heart and Diabetes Institute, Melbourne, Australia. Electronic address: e.levelt@leeds.ac.uk.

Funding

Gadgetron Global Network and Intelligence Computing: Clinical Imaging Application Development and Software InfrastructureZIAHL006214 · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · 2025 to 2025
$1.1M
British Heart Foundation FS/CRTF/20/24003Intramural NIH HHS ZIA HL006214Intramural NIH HHS ZIA HL006242Wellcome Trust
6 · The paper itself

Abstract

backgroundType 2 diabetes (T2D) is characterized by insulin resistance (IR) and dysregulated insulin secretion. Glucagon-like peptide-1 receptor agonist liraglutide promotes insulin secretion, whereas thiazolidinedione-pioglitazone decreases IR.

objectivesThis study aimed to compare the efficacies of increasing insulin secretion vs decreasing IR strategies for improving myocardial perfusion, energetics, and function in T2D via an open-label randomized crossover trial.

methodsForty-one patients with T2D (age 63 years [95% CI: 59-68 years], 27 [66%] male, body mass index 27.8 kg/m

resultsPioglitazone treatment resulted in significant increases in LV mass (96 g [95% CI: 68-105 g] to 105 g [95% CI: 74-115 g]; P = 0.003) and mitral-inflow E/A ratio (1.04 [95% CI: 0.62-1.21] to 1.34 [95% CI: 0.70-1.54]; P = 0.008), and a significant reduction in LV concentricity index (0.79 mg/mL [95% CI: 0.61-0.85 mg/mL] to 0.73 mg/mL [95% CI: 0.56-0.79 mg/mL]; P = 0.04). Liraglutide treatment increased stress myocardial blood flow (1.62 mL/g/min [95% CI: 1.19-1.75 mL/g/min] to 2.08 mL/g/min [95% CI: 1.57-2.24 mL/g/min]; P = 0.01) and myocardial perfusion reserve (2.40 [95% CI: 1.55-2.68] to 2.90 [95% CI: 1.83-3.18]; P = 0.01). Liraglutide treatment also significantly increased the rest (1.47 [95% CI: 1.17-1.58] to 1.94 [95% CI: 1.52-2.08]; P =0.00002) and stress phosphocreatine to adenosine triphosphate ratio (1.32 [95% CI: 1.05-1.42] to 1.58 [95% CI: 1.19-1.71]; P = 0.004) and 6-minute walk distance (488 m [95% CI: 458-518 m] to 521 m [95% CI: 481-561 m]; P = 0.009).

conclusionsLiraglutide treatment resulted in improved myocardial perfusion, energetics, and 6-minute walk distance in patients with T2D, whereas pioglitazone showed no effect on these parameters (Lean-DM [Targeting Beta-cell Failure in Lean Patients With Type 2 Diabetes]; NCT04657939).

Indexed as

Cross-Over StudiesDiabetes Mellitus, Type 2Exercise ToleranceHypoglycemic AgentsLiraglutidePioglitazoneAgedCoronary CirculationFemaleHumansInsulin ResistanceMaleMiddle AgedHypoglycemic AgentsLiraglutidePioglitazonecardiovascular magnetic resonance imagingglucagon like peptide 1 receptor agonistsliraglutidemagnetic resonance spectroscopy, pioglitazonetype 2 diabetes

Identifiers

PMID39084829
PMCPMC11296502

What Socratic holds

Texttitle and abstract
LicenceTDM
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.