Evidence map›Paper›PMID 42096298›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Choice of cardioplegia influences metabolomics of human cardiac tissue.

Sho Tanosaki, Yuan Zhang, Kenneth Bedi, Kenneth Margulies, James E Cox, Zoltan Arany, E Dale Abel

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

7 authors.

Sho TanosakiCardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Yuan ZhangDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of California, Los Angeles, CA 90095.
Kenneth BediCardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Kenneth MarguliesCardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.ORCID 0000-0002-8093-4465
James E CoxDepartment of Biochemistry, University of Utah, Salt Lake City, UT 84112.
Zoltan Arany *Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
E Dale Abel *Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of California, Los Angeles, CA 90095.ORCID 0000-0001-5290-0738

Funding

American Heart Association (AHA) 16SFRN31810000American Heart Association (AHA) 20SFRN35120123American Heart Association (AHA) 857148HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL152446HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL180429Takeda Science Foundation (TSF) NA
6 · The paper itself

Abstract

Cardioplegia is often used prior to acquisition of human cardiac tissue to minimize warm ischemia time, which can severely confound studies of cardiac metabolism. However, there are several choices of cardioplegia solutions, and whether these solutions differentially impact tissue metabolism or metabolomic studies is not known. Here, we perform untargeted metabolomics, using both liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry, on a large cohort of hearts transplanted for cardiomyopathy or from gift-of-life donors, and who have received different cardioplegia solutions. We show that different cardioplegia solutions distinctly impact cardiac metabolism and tissue metabolomic studies. Notably, these differences are mild relative to those seen comparing failing to nonfailing hearts, and identification of cardioplegia components in mass spectra should enable rigorous interpretation of changes between conditions. These data demonstrate how cardioplegia solutions may influence cardiac metabolism in human heart samples and underscore the need to report specific details of cardioplegia solution use in studies of human cardiac metabolism.

Indexed as

Cardioplegic SolutionsHeartHeart Arrest, InducedMetabolomeMetabolomicsMyocardiumFemaleGas Chromatography-Mass SpectrometryHeart TransplantationHumansLiquid Chromatography-Mass SpectrometryMaleCardioplegic Solutionscardioplegiaheart failuremetabolismmetabolomics

Identifiers

PMID42096298
PMCPMC13187823

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.