Evidence map›Paper›PMID 39644170›Full record

ArticleAnnals of neurology2025

Prophylactic Fetal Creatine Supplementation Improves Post-Asphyxial EEG Recovery and Reduces Seizures in Fetal Sheep: Implications for Hypoxic-Ischemic Encephalopathy.

Nhi T Tran, Stacey J Ellery, Sharmony B Kelly, Juliane Sévigny, Madeleine Chatton, Hui Lu, Graeme R Polglase, Rod J Snow, David W Walker, Robert Galinsky

Abstract read
In one paragraph

Article in Annals of neurology, 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. Review
  2. Creatine in women's health: bridging the gap from menstruation through pregnancy to menopause.Journal of the International Society of Sports Nutrition · 2025
    Review
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

10 authors.

Nhi T TranThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.ORCID 0000-0002-0396-9760
Stacey J ElleryThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Sharmony B KellyThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Juliane SévignyThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Madeleine ChattonThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Hui LuThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Graeme R PolglaseThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Rod J SnowInstitute for Physical Activity and Nutrition, Deakin University, Melbourne, Victoria, Australia.
David W WalkerThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.
Robert GalinskyThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria, Australia.

Funding

Cerebral Palsy Alliance ERG02123Jack Brockhoff Foundation (Early Career Grant)National Health and Medical Research Council 1090890National Health and Medical Research Council 1105526National Health and Medical Research Council 1124493National Health and Medical Research Council 1125539National Health and Medical Research Council 1164954
6 · The paper itself

Abstract

objectiveHypoxic-ischemic encephalopathy (HIE) is a major cause of perinatal brain injury. Creatine is a dietary supplement that can increase intracellular phosphocreatine to improve the provision of intracellular adenosine triphosphate (ATP) to meet the increase in metabolic demand of oxygen deprivation. Here, we assessed prophylactic fetal creatine supplementation in reducing acute asphyxia-induced seizures, disordered electroencephalography (EEG) activity and cerebral inflammation and cell death histopathology.

methodsFetal sheep (118 ± 1 days' gestational age [dGA]; 0.8 gestation) were implanted with electrodes to continuously record EEG and nuchal electromyogram activity. At 121 dGA, fetuses were randomly assigned to sham control (i.v. saline infusion without umbilical cord occlusion [UCO]; SalCon), continuous i.v. creatine infusion (6 mg/kg/h; CrUCO) or isovolumetric saline (SalUCO) followed by UCO at 128 ± 2 dGA that lasted until the mean arterial blood pressure reached 19 mmHg. Brain tissue was collected for histopathology after 72 hours of recovery.

resultsCreatine supplementation had no effects on basal systemic or neurological physiology. UCO duration did not differ between CrUCO and SalUCO. After reperfusion, CrUCO fetuses had improved EEG power and frequency recovery and reduced electrographic seizure incidence (SalUCO, 86% vs CrUCO, 29%) and burden. At 72 hours after UCO, cell death in the cerebral cortex and astrogliosis in the periventricular white matter were reduced in CrUCO fetuses compared with SalUCO.

interpretationCreatine supplementation reduced post-asphyxial seizures and improved EEG recovery. Improvements in functional recovery with creatine were associated with regional reductions in cell death and astrogliosis. Prophylactic creatine treatment has the potential to mitigate functional indices of HIE in the late gestation fetal brain. ANN NEUROL 2025;97:673-687.

Indexed as

AsphyxiaCreatineDietary SupplementsHypoxia-Ischemia, BrainSeizuresAnimalsBrainElectroencephalographyFemaleFetusPregnancySheepCreatine

Identifiers

PMID39644170
PMCPMC11889532

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.