Evidence map›Paper›PMID 41602873›Full record

ReviewFrontiers in pediatrics2025

Necrotising enterocolitis biomarkers: a systematic review.

Muhammad Ashhad Faizan, Iffat Khalid, Asten Yeo, Magdalina Mazheda Fadel, Alannah Mcmahon, Philip Gavigan, Saffron O'Neill, Eman Isweisi, Gregana Semova, Edna F Roche and 3 more

Abstract readReview
In one paragraph

Review in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Surgical Interventions for NEC-An Overview.Children (Basel, Switzerland) · 2026
    Review
  2. Review
  3. Article
  4. Article
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

13 authors.

Muhammad Ashhad FaizanDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Iffat KhalidDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Asten YeoDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Magdalina Mazheda FadelDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Alannah McmahonDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Philip GaviganDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Saffron O'NeillDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Eman IsweisiDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Gregana SemovaDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Edna F RocheDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Aoife BranaganDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Judith MeehanDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.
Eleanor J MolloyDepartment of Paediatrics, University of Dublin, Trinity College, Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Necrotising enterocolitis (NEC) is a severe acute inflammatory condition of the gastrointestinal tract that predominantly affects preterm neonates. The variable and often nonspecific clinical signs, followed by rapid progression into fulminant disease, and the lack of standardised definitions and biomarkers, make this condition notoriously difficult to diagnose. This systematic review aims to outline the inflammatory pathways involved in the pathogenesis of NEC and to identify potential biomarkers associated with the initial stages of disease progression. Methods: Following the PRISMA guidelines, we conducted an electronic search of the available literature using the PubMed, Embase, and Cochrane electronic databases with the following search terms ("necrotizing enterocolitis" OR "necrotising enterocolitis" OR "NEC") AND ("biomarker*" OR "biological marker"). Studies reporting data on the diagnostic accuracy of biomarkers for NEC were included. Results were restricted to full-text articles in English, available up to November 2024. Risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) tool. Results: A total of 211 studies were screened, yielding 79 studies for analysis. Most studies evaluated the ability of biomarkers to differentiate Bell's stage ≥II NEC from controls or Bell's stage II from stage III. For identifying Bell's stage ≥II, faecal calprotectin (97.14% sensitivity, 100% specificity) and serum calprotectin (100% sensitivity, 96.4% specificity), as well as a panel consisting of urine proteins including Cystatin C (CST3), Pigment Epithelium Derived Factor (PEDF), and Retinol Binding Protein 4 (RET4) (96% sensitivity, 90% specificity), and maternal human milk oligosaccharide disialyllacto-N-tetraose DSNLT (90% sensitivity and specificity) demonstrated high sensitivity and specificity when sampled prior to or around the initial diagnosis of NEC. Interleukin 33 (IL-33) exhibited high accuracy. Systematic Review Registration: PROSPERO CRD42024307046.

Indexed as

bell's stagingbiomarkerscalprotectinDSNLTinterleukinsNEC (necrotizing enterocolitis)necrotising enterocolitisPEDF

Identifiers

PMID41602873
PMCPMC12833235

What OpenQuestion holds

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Registered trials

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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.