Evidence map›Paper›PMID 39482267›Full record

ArticleESC heart failure2025

Semaglutide normalizes increased cardiomyocyte calcium transients in a rat model of high fat diet-induced obesity.

Vasco Sequeira, Julia Theisen, Katharina J Ermer, Marie Oertel, Anton Xu, David Weissman, Katharina Ecker, Jan Dudek, Martin Fassnacht, Alexander Nickel and 3 more

Abstract read
In one paragraph

Article in ESC heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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.

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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Novel Drug Targets in Diastolic Heart Disease.International journal of molecular sciences · 2025
    Review
  8. 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

13 authors.

Vasco SequeiraDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Julia TheisenDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Katharina J ErmerDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Marie OertelDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Würzburg, Würzburg, Germany.
Anton XuDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
David WeissmanDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Katharina EckerDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Jan DudekDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Martin FassnachtDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Würzburg, Würzburg, Germany.
Alexander NickelDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Michael KohlhaasDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Christoph MaackDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.
Ulrich DischingerDepartment of Translational Science Universitätsklinikum, DZHI, Würzburg, Germany.

Funding

Deutsche Forschungsgemeinschaft 453989101Deutsche Forschungsgemeinschaft 530849567Deutsche Forschungsgemeinschaft Ma.2528/8-1IZKF Würzburg Z-3BC/01
6 · The paper itself

Abstract

aimsObesity increases the risk of heart failure with preserved (HFpEF), but not reduced ejection fraction (HFrEF). The glucagon-like peptide-1 receptor agonist (GLP-1-RA) semaglutide improves outcome of patients with obesity with or without HFpEF, while GLP-1-RAs were associated with adverse outcome in patients with HFrEF. Here, we investigate the effect of in vivo treatment with semaglutide on excitation-contraction coupling in a rat model of obesity. METHODS AND

resultsRats received high-fat/high-fructose diet for 8 weeks and were then randomized to semaglutide (HFD/Sema) or vehicle (HFD/Veh) for another 8 weeks, during which they could choose between HFD and a low-fat/high-fructose diet (LFD). Control rats received either standard chow (CON), HFD or LFD only, without treatment. After 16 weeks, sarcomere shortening and cytosolic Ca

conclusionsWhile HFD increased cardiomyocyte [Ca

Indexed as

CalciumDiet, High-FatGlucagon-Like PeptidesHeart FailureMyocytes, CardiacObesityAnimalsDisease Models, AnimalGlucagon-Like Peptide 1MaleRatsRats, Sprague-DawleySemaglutideStroke VolumeCalciumGlucagon-Like Peptide 1Glucagon-Like PeptidesSemaglutideExcitation‐contraction couplingGlucagon‐like peptide agonistsHeart failureObesitySemaglutide

Identifiers

PMID39482267
PMCPMC11911617

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC
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.