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The Molecular and Histopathological Assessment of Inflammatory Status in Very and Extremely Premature Infants

A Prospective Study

Bibliographic Data

ID15717448
AuthorsClaudia Ioana Borțea (0000-0002-4702-4435, Victor Babeș University of Medicine and Pharmacy Timișoara), Ileana Enătescu (Victor Babeș University of Medicine and Pharmacy Timișoara), Manuela Pantea (0000-0003-2597-3960, Victor Babeș University of Medicine and Pharmacy Timișoara), Mirabela Dima (Victor Babeș University of Medicine and Pharmacy Timișoara), Emil Radu Iacob (0000-0002-5863-6613, Victor Babeș University of Medicine and Pharmacy Timișoara), Cătălin Dumitru (0000-0003-0091-7364, Victor Babeș University of Medicine and Pharmacy Timișoara, corresponding author), Alin Popescu (Victor Babeș University of Medicine and Pharmacy Timișoara), Florina Stoica (0000-0003-4893-856X, Victor Babeș University of Medicine and Pharmacy Timișoara), Rodica Heredea (0000-0001-7634-4297, Clinical Emergency Hospital Bucharest), Daniela Iacob (0000-0003-2468-6003, Victor Babeș University of Medicine and Pharmacy Timișoara)
Year2023
Volume10
Issue2
Pages352-352
Publication date2023-02-10
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children10020352
PMID36832481
OpenAlexW4319962903
LanguageEN
References cited1

Prematurity comes with a varying range of complications, implying a high prevalence of complications and mortality and depending on the severity of prematurity and the sustained inflammation among these infants, which recently sparked an important scientific interest. The primary objective of this prospective study was to establish the degree of inflammation in very (VPIs) and extremely preterm infants (EPIs) in association with the histology findings of the umbilical cord (UC), while the secondary objective was to study the inflammatory markers in the neonates' blood as predictors of fetal inflammatory response (FIR). A total of thirty neonates were analyzed, ten of them being born extremely premature (<28 weeks of gestation) and twenty very premature (28-32 weeks of gestation). The EPIs had considerably higher levels of IL-6 at birth than VPIs (638.2 pg/mL vs. 151.1 pg/mL). The CRP levels at delivery did not vary substantially across groups; however, after days, the EPIs had significantly higher CRP levels (11.0 mg/dL vs. 7.2 mg/dL). In contrast, the LDH was considerably higher in the extremely preterm infants at birth and four days after birth. Surprisingly, the proportions of infants with pathologically increased inflammatory markers did not differ between the EPIs and VPIs. The LDH increased considerably in both groups, although the CRP levels increased exclusively among the VPIs. The stage of inflammation in the UC did not vary substantially between the EPIs and VPIs. The majority of infants were identified with Stage 0 UC inflammation (40% in EPI vs. 55% in VPIs). There was a substantial correlation link between gestational age and newborn weight and a significant inverse correlation among gestational age and IL-6 and LDH levels. There was a strong negative association between weight and IL-6 (rho = -0.349) and LDH (rho = -0.261). The stage of the UC inflammation demonstrated a statistically significant direct connection with IL-6 (rho = 0.461) and LDH (rho = 0.293), but none with the CRP. Further studies involving a bigger population size of preterm newborns are required to validate the findings and analyze more inflammatory markers, while prediction models on inflammatory markers that are measured expectantly, before the onset of preterm labor, need to be created

Biology · Cord blood · Fetus · Gestation · Gestational age · Inflammation · Obstetrics · Pregnancy · Premature birth · Prospective cohort study · Stage (stratigraphy · Systemic inflammation · Umbilical cord · Infant Nutrition and Health · Medicine · Neonatal Respiratory Health Research · Preterm Birth and Chorioamnionitis · Gastroenterology · Immunology · Internal Medicine · Pediatrics · Physiology

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