Evidence map›Paper›PMID 40295408›Full record

ArticleEuropean journal of pediatrics2025

The predictive value of maternal and neonatal inflammatory biomarkers for necrotizing enterocolitis.

Melinda Matyas, Tamás Ilyés, Madalina Valeanu, Alexandra M Crăciun, Monica Hășmășanu, Nicoleta Grosu, Gabriela Zaharie

Abstract read
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Necrotizing Enterocolitis: What's New and What's Next?International journal of molecular sciences · 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

7 authors.

Melinda MatyasNeonatology Department, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania. melimatyas@yahoo.com.
Tamás IlyésDepartment of Molecular Sciences, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Madalina ValeanuMedical Informatics and Biostatistics Department, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Alexandra M CrăciunDepartment of Molecular Sciences, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Monica HășmășanuNeonatology Department, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Nicoleta GrosuNeonatology Department, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Gabriela ZaharieNeonatology Department, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than half of preterm births are triggered by inflammatory processes at the foeto-maternal interface. These inflammatory processes can persist after birth due to the unique vulnerabilities of preterm infants, often resulting in sustained inflammation with a role in complications such as bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), intraventricular hemorrhage (IVH), and periventricular leukomalacia (PVL). The aim of this study was to evaluate the predictive value of maternal inflammatory status, assessed through biomarkers of inflammation (CRP, chorioamnionitis, preeclampsia), and neonatal inflammatory markers (CRP 1, CRP 2, PCT, IL3, MMP9) on the incidence of NEC in preterm neonates. We conducted a prospective longitudinal study in the 1st Neonatology Department, Cluj-Napoca, Romania. A total of 82 preterm newborns (gestational age < 34 weeks + 6 days) were enrolled in the study. Interleukin-3 (IL3) and matrix metalloproteinase-9 (MMP9) levels were measured using the ELISA technique. Additionally, C-reactive protein (CRP) and procalcitonin (PCT) were measured in the first days of life. The correlation between these inflammatory markers and the incidence of NEC was analyzed. Furthermore, we examined the role of maternal inflammation and chorioamnionitis in relation to NEC incidence. Out of the 82 neonates enrolled, 20 developed NEC. Neonates who developed NEC had higher IL3 levels at birth. A significant positive correlation was found between maternal CRP levels and neonatal IL3 levels (r = 0.541, p < 0.001). In the NEC group, maternal CRP levels were also elevated compared to those in neonates who did not develop NEC.

conclusionNeonatal inflammation is associated with an increased incidence of NEC. Prenatal inflammatory conditions appear to trigger a persistent inflammatory process in preterm neonates, raising the risk of NEC. WHAT IS KNOWN: • NEC is a multifactorial disease of preterm newborn with multiple maternal and neonatal risk factors. WHAT IS NEW: • Evaluate the probability of NEC at preterm neonates of mothers with ongoing inflammatory conditions during pregnancy.

Indexed as

ChorioamnionitisEnterocolitis, NecrotizingInfant, Premature, DiseasesInflammationAdultBiomarkersC-Reactive ProteinFemaleHumansIncidenceInfant, NewbornInfant, PrematureLongitudinal StudiesMaleMatrix Metalloproteinase 9Predictive Value of TestsBiomarkersC-Reactive ProteinMatrix Metalloproteinase 9ProcalcitoninBiomarkerInflammationNecrotizing enterocolitisPreterm birth

Identifiers

PMID40295408
PMCPMC12037420

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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.