Evidence map›Paper›PMID 41286887›Full record

ArticleJournal of translational medicine2025

Urinary metabolome at birth in patients with hypoxic-ischemic encephalopathy treated with therapeutic hypothermia and long-term neurodevelopmental outcomes: a 7-year follow up.

Claudio Ancona, Enrico Valerio, Nicoletta Mainini, Alessio Favali, Ignazio D'Errico, Chiara Lasagni, Matteo Stocchero, Paola Pirillo, Giuseppe Giordano, Stefano Sartori and 1 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

Claudio Ancona *Pediatric Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University of Padua, Padua, Italy.
Enrico Valerio *Neonatal Intensive Care Unit, Department of Women's and Children's Health, University of Padua, Via Giustiniani 3, 35128, Padua, Italy.
Nicoletta MaininiNeonatal Intensive Care Unit, Department of Women's and Children's Health, University of Padua, Via Giustiniani 3, 35128, Padua, Italy.
Alessio FavaliNeonatal Intensive Care Unit, Department of Women's and Children's Health, University of Padua, Via Giustiniani 3, 35128, Padua, Italy.
Ignazio D'ErricoDepartment of Neuroradiology, Azienda Ospedale-Università di Padova, Padua, Italy.
Chiara LasagniDepartment of Women's and Children's Health, University of Padua, Padua, Italy.
Matteo StoccheroInstitute of Pediatric Research "Città della Speranza", Padua, Italy.
Paola PirilloInstitute of Pediatric Research "Città della Speranza", Padua, Italy.
Giuseppe GiordanoInstitute of Pediatric Research "Città della Speranza", Padua, Italy.
Stefano SartoriPediatric Neurology and Neurophysiology Unit, Department of Women's and Children's Health, University of Padua, Padua, Italy.
Eugenio BaraldiNeonatal Intensive Care Unit, Department of Women's and Children's Health, University of Padua, Via Giustiniani 3, 35128, Padua, Italy. eugenio.baraldi@unipd.it.ORCID 0000-0001-7454-157X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxic-ischemic encephalopathy (HIE) is a leading cause of neonatal mortality and morbidity, yet no validated biomarkers currently exist to predict long-term outcomes. We investigated the potential of the neonatal urinary metabolomic profile as a predictor of long-term neurodevelopmental outcomes in HIE newborns treated with therapeutic hypothermia (TH).

methodsWe conducted a longitudinal study in neonates with HIE undergoing TH. Urine samples collected during TH were analyzed using untargeted metabolomics via mass spectrometry. Based on long-term follow-up outcomes, patients were categorized into two groups: the adverse outcome (AO) group, defined by perinatal death, cerebral palsy, and/or an intelligence quotient (IQ) < 70, and the favourable outcome (FO) group, defined as absence of CP and IQ ≥ 70. Additionally, we assessed the predictive value of early neonatal brain magnetic resonance imaging (MRI) in relation to the aforementioned outcomes.

resultsAmong 53 newborns treated with TH for HIE, long-term follow-up outcomes were available for 40; 29 were classified as FO and 11 as AO group. To mitigate bias, 11 FO patients were matched with 11 AO patients based on similar perinatal characteristics. Metabolomic analysis identified 21 metabolites distinguishing the two groups, with γ-butyrolactone, N-acetyl-galactosamine/glucosamine, Aldosterone, and Creatinine showing independent discriminative capability among groups. Brain MRI demonstrated a 67% positive and 96% negative predictive value for adverse outcomes.

conclusionsThe identified metabolites are implicated in neuromodulation and neuronal susceptibility to damage, suggesting their potential as prognostic markers for long-term outcomes in HIE and warranting further investigation. This is the first study linking the acute-phase metabolomic profile with long-term neurodevelopmental outcomes in HIE neonates, supporting its prognostic potential.

Indexed as

Hypothermia, InducedHypoxia-Ischemia, BrainMetabolomeFemaleFollow-Up StudiesHumansInfant, NewbornLongitudinal StudiesMagnetic Resonance ImagingMaleMetabolomicsTreatment OutcomeHypoxic–ischemic encephalopathyLong-term neurodevelopmental outcomesMetabolomicsNewbornTranslational research

Identifiers

PMID41286887
PMCPMC12645678

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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.