Observational studyMedicine2025
Comparisons of fecal microbiota and cytokines in preterm infants preceding necrotizing enterocolitis and feeding intolerance: An observational study.
Observational study in Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
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Who cites it
2 citing papers in PubMed.
- Gut Microbiome in Neonatal Necrotizing Enterocolitis - A Comprehensive Review of Evidence.Indian journal of pediatrics · 2026Review
- Mechanisms by which tryptophan metabolites enhance intestinal barrier function to prevent necrotizing enterocolitis in preterm infants.Frontiers in immunology · 2026Review
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
To facilitate earlier detection of necrotizing enterocolitis (NEC), we compared serum cytokines and fecal microbiota composition in preterm infants prior to the occurrence of NEC, with those exhibiting feeding intolerance (FI) or unaffected controls. Fecal microbiota and early serum cytokines in preterm infants were analyzed and compared. The gestational age (GA) at birth and birth weight did not differ among the groups, averaging 29.5 weeks and 1289.0 g, respectively. Respiratory distress syndrome (RDS, P = .010) and intraventricular hemorrhage (P = .047) were more commonly observed in the NEC group compared to others. There were no significant differences in the serum concentrations of various cytokines among the 3 groups. Individual variability in fecal microbial compositions was noted. No significant differences were observed in the alpha and beta diversities in fecal microbiota among the groups. TNFα showed a negative correlation with the abundant microbiota in feces of preterm infants. Rather than early intestinal dysbiosis or alterations in serum cytokines, meticulous monitoring for signs in preterm infants experienced clinical instability in early transitional period remains crucial for timely diagnosis of NEC. Serum cytokines may be associated with the development of gut microbiota in preterm infants, suggesting the need for further comprehensive study.
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