Evidence map›Paper›PMID 41717916›Full record

ArticleJournal of the American Heart Association2026

Circulating Ketone Bodies and Incident Cardiovascular Outcomes and Mortality: Insights From the UK Biobank.

Parag Anilkumar Chevli, Saeid Mirzai, Richard Kazibwe, Jeff Kingsley, Alexis C Wood, Joseph Yeboah, Leandro Slipczuk, Anurag Mehta, Harpreet S Bhatia, Ambarish Pandey and 1 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

11 authors.

Parag Anilkumar ChevliDepartment of Cardiovascular Medicine Wake Forest University School of Medicine Winston-Salem NC USA.ORCID 0000-0002-4084-8175
Saeid MirzaiDepartment of Cardiovascular Medicine Wake Forest University School of Medicine Winston-Salem NC USA.ORCID 0000-0002-2579-4965
Richard KazibweSection on Hospital Medicine, Department of Internal Medicine Wake Forest University School of Medicine Winston-Salem NC USA.ORCID 0000-0001-7085-3373
Jeff KingsleyDepartment of Cardiovascular Medicine Wake Forest University School of Medicine Winston-Salem NC USA.
Alexis C WoodUSDA/ARS Children's Nutrition Research Center Baylor College of Medicine Houston TX USA.ORCID 0000-0001-7616-2119
Joseph YeboahDepartment of Cardiovascular Medicine Wake Forest University School of Medicine Winston-Salem NC USA.ORCID 0000-0001-6274-5882
Leandro SlipczukDivision of Cardiology Montefiore Healthcare Network/Albert Einstein College of Medicine New York NY USA.ORCID 0000-0003-3091-3735
Anurag MehtaVCU Health Pauley Heart Center and Division of Cardiology, Department of Internal Medicine Virginia Commonwealth University School of Medicine Richmond VA USA.ORCID 0000-0002-6910-5551
Harpreet S BhatiaDivision of Cardiovascular Medicine, Department of Medicine University of California San Diego La Jolla CA USA.ORCID 0000-0002-3964-2989
Ambarish PandeyDivision of Cardiology, Department of Internal Medicine University of Texas Southwestern Medical Center Dallas TX USA.ORCID 0000-0001-9651-3836
Michael D ShapiroCenter for the Prevention of Cardiovascular Disease, Department of Cardiovascular Medicine Wake Forest University School of Medicine Winston-Salem NC USA.ORCID 0000-0002-9071-3287

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKetone bodies (KB) are endogenous energy sources synthesized by the liver in response to metabolic stress. Their associations with atherosclerotic cardiovascular disease (ASCVD), heart failure (HF), and mortality and their potential beneficial or harmful effects have yet to be determined. This study aimed to examine the association between KB and incident cardiovascular outcomes and mortality in a large general population cohort free from ASCVD and HF at baseline.

methodsThis analysis included 90 987 participants (mean age 56.4 ± 8.1 years; 54.7% women) from the UK Biobank without prevalent ASCVD or HF. KB were measured by nuclear magnetic resonance spectroscopy. The primary outcomes were ASCVD, HF, and all-cause death. Secondary outcomes were myocardial infarction, ischemic stroke, peripheral artery disease, and CVD death. All outcomes were defined based on

resultsAt a median follow-up of 13.4 years, higher levels of total KB (per 10-fold increase) were associated with a greater risk of incident ASCVD, HF, and all-cause mortality (hazard ratio [HR], 1.31 [95% CI, 1.18-1.46], 1.44 [95% CI, 1.24-1.6]7, and 1.51 [95% CI, 1.38-1.66]), respectively. Participants also demonstrated a 37% (95% CI, 11%-69%) increased risk of stroke and 69% (95% CI, 43%-100%) increased risk of CVDdeath. There was no significant association between KB and incident myocardial infarction.

conclusionsElevation in endogenous KB in a population free from CVD at baseline is associated with an increased risk of ASCVD, HF, stroke, and mortality.

Indexed as

Cardiovascular DiseasesKetone BodiesAgedBiological Specimen BanksBiomarkersCause of DeathFemaleHumansIncidenceMaleMiddle AgedRisk AssessmentRisk FactorsUK BiobankUnited KingdomBiomarkersKetone Bodiesatherosclerotic cardiovascular diseaseheart failureketone bodiesmortality

Identifiers

PMID41717916
PMCPMC13055806

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Registered trials

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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.