Evidence map›Paper›PMID 42350770›Full record

SynthesisPediatric research2026

Cord blood biomarkers in infants with neonatal encephalopathy: a systematic review and meta-analysis.

Dimitrios Rallis, Magdalena Smolkova, Brian Henry Walsh, Deirdre Murray, Helen Christou, Mohamed El-Dib

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Pediatric research, 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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Dimitrios RallisFaculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece. drallis@auth.gr.
Magdalena SmolkovaSchool of Clinical Medicine, University of Cambridge, Cambridge, UK.
Brian Henry WalshINFANT Research Centre, University College Cork, Cork, Ireland.
Deirdre MurrayINFANT Research Centre, University College Cork, Cork, Ireland.
Helen ChristouDivision of Newborn Medicine, Mass General Brigham, Harvard Medical School, Boston, MA, USA.
Mohamed El-DibDivision of Newborn Medicine, Mass General Brigham, Harvard Medical School, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceCord blood biomarkers could aid in the early diagnosis of neonatal encephalopathy (NE) and detect neonates likely to benefit from interventions.

methodsA systematic review and meta-analysis were conducted. PubMed, Scopus, OVID MEDLINE, Embase, and Cochrane were searched through July 2024. Eligible studies were prospective, retrospective, longitudinal, or cross-sectional in English. Reviews, case series, case-control, and opinion articles were excluded. Standardized mean differences were calculated with random-effects models; heterogeneity was assessed with I² and bias with Egger's test.

resultsOf 1705 studies screened, 63 were reviewed and 49 meta-analyzed, covering 51 cord blood biomarkers, metabolomic profiles, and microRNA/mRNA expression profiles. Several biomarkers were significantly elevated in neonates with NE compared to controls, including tumor necrosis factor-alpha (3.34; 95%CI 2.52-4.15), prooxidant-antioxidant balance (0.80; 95%CI 0.59-1.00), activin-A (0.88; 95%CI 0.52-1.24), troponin (6.13; 95%CI 3.33-8.93), S100 calcium-binding protein B (2.74; 95%CI 0.94-4.54), glial fibrillary acidic protein, neuron-specific enolase, tau, neurofilament light protein, interleukin-6, interleukin-1, malondialdehyde, hypoxanthine, and nucleated red blood cells. Metabolomic changes and altered miRNA expression were also reported.

conclusionsEarly detection of specific cord blood biomarkers shows promise for NE diagnosis. Further prospective studies are needed to validate biomarker panels for clinical use. IMPACT: Early detection of specific cord blood biomarkers may help identifying neonates with neonatal encephalopathy (NE). Tumor necrosis factor-alpha (TNF-α), prooxidant-antioxidant balance, nucleated red blood cells, and activin-A were significantly elevated in neonates with NE compared to controls. S100 calcium-binding protein B (S100B) and IL-6 were higher in neonates with moderate/severe NE compared to neonates with mild NE. TNF-α, prooxidant-antioxidant balance, nucleated red blood cells, activin-A, S100B, and IL-6 are the most promising cord blood biomarkers for early diagnosis and disease severity assessment of NE.

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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.