Evidence map›Paper›PMID 40181520›Full record

ArticleThe Journal of physiology2026

Ketogenic diet and ketone salts differentially improve cardiometabolic complications in an HFpEF rat model.

Alexandre Gonçalves, Inês N Alves, Cláudia Mendes, Daniela Miranda, Glória Conceição, João Almeida-Coelho, Diana Martins, Isabel Miranda, Alexandre Rodrigues, Carolina Silva and 8 more

Abstract read
In one paragraph

Article in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. 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

18 authors.

Alexandre GonçalvesDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-5386-8378
Inês N AlvesDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0001-8329-3758
Cláudia MendesDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-4452-6149
Daniela MirandaDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
Glória ConceiçãoRISE-Health, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-7986-2425
João Almeida-CoelhoDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-3769-8962
Diana MartinsDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0003-4536-2315
Isabel MirandaDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
Alexandre RodriguesDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
Carolina SilvaDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0009-0008-0442-3947
Sandra Marisa OliveiraDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
José SerenoFaculty of Medicine, University of Coimbra, Coimbra, Portugal.
Maria João FerreiraFaculty of Medicine, University of Coimbra, Coimbra, Portugal.ORCID https://orcid.org/0000-0001-8952-8618
Ulrich DischingerDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Würzburg, Würzburg, Germany.
Henrique GirãoFaculty of Medicine, University of Coimbra, Coimbra, Portugal.ORCID https://orcid.org/0000-0002-5786-8447
Adelino F Leite-MoreiraDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
Vasco SequeiraDepartment of Translational Science, DZHI, Universitätsklinikum Würzburg, Würzburg, Germany.ORCID https://orcid.org/0000-0002-9192-7674
Inês Falcão-PiresDepartment of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0003-1937-3782

Funding

Deutsche Forschungsgemeinschaft (DFG) 530849567Foundation for Science and Technology (FST) SFRH/BD/145203/2019
6 · The paper itself

Abstract

Heart failure with preserved ejection fraction (HFpEF) remains a major health concern with limited therapeutic options. Growing evidence supports the multiple benefits of ketones in heart disease, but their impact on HFpEF remains unknown. We investigated whether increasing ketones can help to manage HFpEF. Using the ZSF1 rat model of HFpEF, 16-week-old rats were randomly assigned to one of three subgroups: (i) control diet; (ii) ketogenic diet (KD); or (iii) control diet with added exogenous ketone salts (KS) in their drinking water for 10 weeks. We found that both KD and KS ameliorated the HFpEF phenotype by improving structural echocardiographic parameters, lowering glycaemia and lipid profiles, and reducing HFpEF-related fibrosis and hypertrophy without impacting in vivo diastolic function. Nevertheless, ex vivo cardiomyocyte preparations showed improved calcium handling and myofilament relaxation, suggesting benefits at the cellular level. Interestingly, KD still proved effective, despite the potentially adverse increase in fat mass. There was decreased myofilament Ca

Indexed as

Diet, KetogenicHeart FailureKetonesAnimalsDisease Models, AnimalMaleMyocytes, CardiacRatsStroke VolumeKetonesheart failureheart failure with preserved ejection fractionketogenic dietketonesketone salts

Identifiers

PMID40181520
PMCPMC13480996

What OpenQuestion 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 OpenQuestion graph.