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Updated: Jun 5, 2026

A Neonatal BALB/c Mouse Model of Necrotizing Enterocolitis
Published on: November 30, 2021
Necrotizing enterocolitis is associated with neonatal intestinal injury
Kristyn Mannoia1, Danilo S Boskovic, Laurel Slater
1Division of Pediatric Surgery, Loma Linda University School of Medicine, Loma Linda, CA 92354, USA.
Premature infants with elevated urinary intestinal fatty acid binding protein (iFABP(u)) show subclinical intestinal injury. This marker may help identify high-risk newborns for necrotizing enterocolitis (NEC) and guide preventive care.
Area of Science:
- Neonatology
- Gastroenterology
- Biomarker Research
Background:
- Necrotizing enterocolitis (NEC) is a serious condition affecting premature infants.
- Subclinical intestinal injury may precede NEC development.
- Early identification of at-risk infants is crucial for timely intervention.
Purpose of the Study:
- To investigate the hypothesis that subclinical intestinal mucosal compromise predisposes premature newborns to NEC.
- To assess the utility of urinary intestinal fatty acid binding protein (iFABP(u)) as a marker for intestinal injury in neonates.
- To determine if elevated iFABP(u) is associated with the subsequent development of NEC.
Main Methods:
- Fifty-five premature newborns (23-36 weeks gestational age) were enrolled.
- Urine samples were collected within the first 90 hours of life.
- Urinary iFABP(u) concentrations were measured; NEC diagnosis was based on clinical, pathological, and/or imaging findings.
Main Results:
- Elevated neonatal iFABP(u) (>800 pg/mL) was observed in 27 infants.
- All 9 infants who developed stage 2 or 3 NEC had elevated iFABP(u).
- Increased iFABP(u) levels, unlike asphyxia, were significantly associated with NEC development (P < .01).
Conclusions:
- A significant incidence of intestinal mucosal compromise was found in premature infants.
- Elevated neonatal iFABP(u) was consistently observed in infants who later developed NEC.
- Neonatal iFABP(u) may serve as a valuable tool for identifying high-risk infants and enabling targeted preventive strategies for NEC.
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