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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Faecal eosinophil cationic protein and serum immunoglobulin E in relation to infant feeding practices
Man-Chin Hua1,2, Chien-Chang Chen2,3, Sui-Ling Liao1,2
11 Department of Pediatrics, Chang Gung Memorial Hospital, Keelung, Taiwan.
Insights
Exclusive breastfeeding for over six months may increase infant intestinal inflammation, not prevent allergies. Early introduction of solids at 5-6 months showed lower inflammation markers. Faecal eosinophil cationic protein did not correlate with immunoglobulin E levels.
Area of Science:
- Pediatric Allergy and Immunology
- Gastroenterology
- Infant Nutrition
Background:
- The impact of breastfeeding duration and solid food introduction timing on allergy prevention remains uncertain.
- Investigating infant feeding practices and their influence on intestinal inflammation is crucial for allergy prevention strategies.
Purpose of the Study:
- To evaluate the effect of exclusive breastfeeding duration and solid food introduction timing on intestinal inflammation in infants.
- To determine if faecal eosinophil cationic protein (f-ECP) is associated with serum immunoglobulin E (IgE) levels in infants.
Main Methods:
- Utilized data from the Prediction of Allergies in Taiwanese CHildren (PATCH) birth cohort study with 206 infants.
- Collected stool samples at 6 and 12 months for f-ECP analysis and blood samples at 12 months for total and allergen-specific IgE.
- Compared f-ECP and IgE levels based on exclusive breastfeeding duration and timing of solid food introduction.
Main Results:
- Exclusively breastfed infants showed significantly higher f-ECP at 6 months compared to formula-fed or non-exclusively breastfed infants.
- Infants introduced to solid foods between 5-6 months had the lowest f-ECP levels at 12 months.
- No significant association was found between f-ECP and total or specific serum IgE levels.
Conclusions:
- Exclusive breastfeeding for over 6 months did not reduce serum IgE but was associated with increased intestinal inflammation.
- Faecal eosinophil cationic protein may not be a reliable indicator of IgE sensitization in infancy.
- Optimizing the timing of solid food introduction alongside breastfeeding warrants further investigation for allergy prevention.
Abstract:
Background To date, the effects of exclusive breastfeeding duration and timing of solid food introduction on allergy prevention are unclear. The aim of this study was to determine the effect of variable feeding practices on intestinal inflammation in infants using faecal eosinophil cationic protein as a surrogate marker and to assess whether faecal eosinophil cationic protein is associated with serum immunoglobulin E. Methods Subjects ( n = 206) were enrolled from the Prediction of Allergies in Taiwanese CHildren (PATCH) birth cohort study. Stool samples were collected at 6 and 12 months for determining eosinophil cationic protein, and blood was collected for determining total and allergen-specific immunoglobulin E at 12 months. We compared these biomarkers between infants with variable exclusive breastfeeding duration and infants introduced to solid foods at various periods. The association between faecal eosinophil cationic protein, total serum immunoglobulin E and specific immunoglobulin E was also analysed. Results Faecal eosinophil cationic protein was significantly higher in exclusively breastfed infants compared with formula-fed infants and infants who were not exclusively breastfed at 6 months of age ( P < 0.05). At 12 months, infants who were introduced to solid foods at 5-6 months had the lowest faecal eosinophil cationic protein compared with those who were introduced at earlier and later periods. There was no significant association between faecal eosinophil cationic protein and serum immunoglobulin E. Conclusion We found that breastfeeding exclusively for >6 months did not reduce serum immunoglobulin E, but rather increased intestinal inflammation. Faecal eosinophil cationic protein was not associated with total serum immunoglobulin E and specific immunoglobulin E and might not be a useful indictor of immunoglobulin E sensitization in infancy.
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