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New research · Allergy & Immunology
BMC gastroenterology · 1d
Cohort studyBMC gastroenterology · 2026

Age-adjusted eosinophilia in preterm infants with feeding intolerance: a retrospective cohort study.

Ozge Serce Pehlevan, Merve Cekildas, Ayla Gunlemez
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Allergy & ImmunologyCohort study

Age-adjusted eosinophilia is associated with higher odds of feeding intolerance in preterm infants.

Age-adjusted eosinophilia in preterm infants with feeding intolerance: a retrospective cohort study.

Ozge Serce Pehlevan et al. · BMC gastroenterology · 2026
Background

Feeding intolerance (FI) remains diagnostically challenging because of nonspecific symptoms and overlap with multiple gastrointestinal conditions.

Purpose

This study investigated the association between peripheral eosinophilia and FI in preterm infants with exploratory evaluation of necrotizing enterocolitis (NEC) and cow's milk protein-related gastrointestinal disease in relation to eosinophilia.

Methods

In this retrospective cohort study, 122 preterm infants (< 34 weeks' gestation, < 2000 g) with eosinophil counts ≥ 700/mm³ were included.

n = 100 infants
Results

preterm infants with high eosinophil counts had much higher odds of feeding problems

OR 6 (95% CI 1.32 to 27.26)
null = 11.3227.26
CI excludes the null - significant
More results

Age-adjusted eosinophilia was present in 100 infants.

All 13 NEC cases occurred in eosinophilic infants, although the temporal relationship between eosinophilia and NEC varied.

More results

Suspected cow's milk protein-related gastrointestinal disease was identified in 11 infants, all of whom showed clinical improvement following dietary elimination.

“
Conclusion · 1 of 3

Age-adjusted eosinophilia was frequently observed in preterm infants with FI and more severe gastrointestinal manifestations.

Conclusion · 2 of 3

While unlikely to be causally related to FI, it may reflect an accompanying immune or inflammatory response during gastrointestinal disease.

Conclusion · 3 of 3

Eosinophil counts may provide supportive information in selected infants with persistent FI or NEC-like presentations, particularly when alternative inflammatory gastrointestinal processes are being considered.

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