Evidence map›Paper›PMID 42206795›Full record

ArticleJACC. Advances2026

Perioperative Metabolomic Profiling in Neonatal Cardiac Surgery Identifies a High-Risk Phenotype for Adverse Outcomes.

Sean J Cooney, Bhargava K Chinni, Eric M Graham, Mark Russell, Brian W McCrindle, Cedric Manlhiot, Kurt W Prins, Allen D Everett, David R Graham

Abstract read
In one paragraph

Article in JACC. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Sean J CooneyBlalock-Taussig-Thomas Congenital Heart Center, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland, USA.
Bhargava K ChinniBlalock-Taussig-Thomas Congenital Heart Center, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland, USA.
Eric M GrahamDivision of Pediatric Cardiology, Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina, USA.
Mark RussellUniversity of Michigan, Ann Arbor, Michigan, USA.
Brian W McCrindleThe Labatt Family Heart Centre, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, Canada.
Cedric ManlhiotBlalock-Taussig-Thomas Congenital Heart Center, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland, USA.
Kurt W PrinsGazes Cardiac Research Institute, Medical University of South Carolina, Charleston, South Carolina, USA.
Allen D EverettBlalock-Taussig-Thomas Congenital Heart Center, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland, USA. Electronic address: aeveret3@jhmi.edu.
David R GrahamGraham Scientific, Germantown, Maryland, USA. Electronic address: david.graham@grahamscientific.us.

Funding

GP130 Antagonism in Porcine RV Pressure OverloadR01HL162927 · NHLBI · UNIVERSITY OF MINNESOTA · PI Kurt W Prins · 2022 to 2026
$3.3M
Multi-scale Investigation of Sex Differences in Right Ventricular Function via Estrogen-Microtubule InteractionsR01HL158795 · NHLBI · UNIVERSITY OF MINNESOTA · PI Kurt W Prins · 2022 to 2026
$2.8M
NHLBI NIH HHS R01 HL158795NHLBI NIH HHS R01 HL162927
6 · The paper itself

Abstract

backgroundNeonatal cardiac surgery is associated with high morbidity and mortality. Perioperative metabolic stress may result in distinct metabolic phenotypes associated with adverse clinical outcomes.

objectivesThe purpose of this study was to identify perioperative metabolomic phenotypes associated with adverse clinical outcomes in neonates undergoing cardiac surgery with cardiopulmonary bypass (CPB).

methodsPlasma samples were collected from 230 neonates at 3 institutions at preoperative, post-CPB, and 24-hour time points. Targeted metabolomics was performed via mass spectrometry. Feature selection used the Boruta algorithm, and unsupervised hierarchical clustering (Euclidean distance, Ward's linkage) identified phenotypes. The primary endpoint was a composite of morbidity, including death, extracorporeal membrane oxygenation, cardiac arrest, renal replacement therapy, hepatic injury, elevated lactate, and low cardiac output syndrome.

resultsFifty-one of 76 metabolites passed quality control. Unsupervised clustering identified 3 metabolomic groups with composite outcome rates of 40%, 6.1%, and 58%. For clinical interpretation, these corresponded to intermediate-, low-, and high-risk phenotypes, respectively. The high-risk phenotype was characterized by elevated 24-hour tyrosine, alanine, proline, and methionine, metabolites linked to amino acid catabolism and inflammation. The low-risk phenotype demonstrated higher post-CPB cystine and greater pre/post ratios of galactitol and acetylcarnitine, consistent with preserved redox balance and fatty acid oxidation. Multiple comparison adjustments confirmed associations between these metabolic pathways and clinical outcomes.

conclusionsMetabolomic profiling identified phenotypes associated with risk for adverse outcomes after neonatal cardiac surgery. Amino acid catabolism and inflammatory pathways were linked to morbidity, supporting further evaluation of metabolomic biomarkers for perioperative risk stratification and targeted therapeutic intervention.

Indexed as

amino acid metabolismcardiopulmonary bypassmetabolomicsneonatal cardiac surgerypostoperative outcomesrisk stratification

Identifiers

PMID42206795
PMCPMC13221857

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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.