Evidence map›Paper›PMID 42286641›Full record

Trial reportCardiovascular diabetology2026

The effect of empagliflozin on inflammation in patients with overweight or obesity and risk of heart failure: a substudy from the Empire Prevent Metabolic trial.

Camilla Fuchs Andersen, Julie Hempel Larsen, Massar Omar, Nina Nouhravesh, Caroline Kistorp, Christian Tuxen, Filip K Knop, Julie Lyng Forman, Filip Soeskov Davidovski, Lars Køber and 5 more

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

Trial report in Cardiovascular diabetology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT05042973. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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.

NCT05042973 phase2completed

Empagliflozin to Elderly and Obese Patients With Cardiovascular Disease (Empire Prevent: Metabolic): A Randomized Controlled Trial

Ran2021Enrolled165Registered outcomes16Posted comparisons0ConditionsHeart Failure, ObesityArmsempagliflozin 10 mg, Placebo
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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Camilla Fuchs AndersenDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark.
Julie Hempel LarsenDepartment of Cardiology, Odense University Hospital, Odense, Denmark.
Massar OmarDepartment of Cardiology, Odense University Hospital, Odense, Denmark.
Nina NouhraveshDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark.
Caroline KistorpDepartment of Endocrinology and Metabolism, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.
Christian TuxenDepartment of Cardiology, Copenhagen University Hospital-Frederiksberg and Bispebjerg, Copenhagen, Denmark.
Filip K KnopDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Julie Lyng FormanSection of Biostatistics, Department of Public Health, University of Copenhagen University, Copenhagen, Denmark.
Filip Soeskov DavidovskiDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark.
Lars KøberDepartment of Cardiology, The Heart Center, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.
Rugivan SabaratnamSteno Diabetes Center Odense, Odense University Hospital, Odense, Denmark.
Kurt HøjlundSteno Diabetes Center Odense, Odense University Hospital, Odense, Denmark.
Morten SchouDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark. morten.schou.04@regionh.dk.
Jacob Eifer MøllerDepartment of Cardiology, The Heart Center, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.
Jesper JensenDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Herlev Ringvej 75, 2730, Herlev, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity increases the risk of heart failure (HF), potentially through low-grade inflammatory processes. Sodium-glucose co-transporter 2 (SGLT2) inhibitors have been suggested to attenuate inflammation, although data in patients without diabetes and HF are lacking. Moreover, it is unknown whether SGLT2 inhibitors affect adipose tissue dysfunction. We aimed to investigate the effect of the SGLT2 inhibitor empagliflozin on systemic inflammation, uric acid, and adipose tissue dysfunction in high-risk patients with overweight or obesity.

methodsPre-defined secondary analysis of the Empire Prevent Metabolic trial. Outpatients with body mass index (BMI) > 28 kg/m

resultsWe randomised 92 patients (empagliflozin: 44, placebo: 48). Median age was 68 years, median BMI was 31.6 kg/m

conclusionsIn this study, empagliflozin did not demonstrate anti-inflammatory effects but yielded possibly meaningful uricosuric effects in non-diabetic patients with overweight or obesity. Moreover, adipose tissue dysfunction remained unaltered. Trial registration clinicaltrials.gov NCT05042973.

Indexed as

Anti-Inflammatory AgentsBenzhydryl CompoundsGlucosidesHeart FailureInflammationInflammation MediatorsObesitySodium-Glucose Transporter 2 InhibitorsAdiposityAgedBiomarkersFemaleHumansMaleMiddle AgedRisk AssessmentAnti-Inflammatory AgentsBenzhydryl CompoundsBiomarkersempagliflozinGlucosidesInflammation MediatorsSodium-Glucose Transporter 2 InhibitorsUric AcidAdipose tissue dysfunctionElderlyEmpagliflozinHeart failureInflammationObesityPreventionSodium-glucose co-transporter 2 inhibitorsUric acid

Identifiers

PMID42286641
PMCPMC13483855

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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.