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Updated: Feb 13, 2026

Murine Fecal Isolation and Microbiota Transplantation
Published on: May 26, 2023
Early fecal microbiota composition in children who later develop celiac disease and associated autoimmunity
Anniina Rintala1,2, Iiris Riikonen1, Anne Toivonen3,4
1a Department of Medical Microbiology and Immunology , University of Turku , Turku , Finland.
Insights
Early gut bacteria composition in infants does not predict celiac disease (CD) development. This study found no significant differences in fecal microbiota between children who later developed CD and healthy controls.
Area of Science:
- Gastroenterology
- Microbiology
- Immunology
Background:
- Intestinal microbiota composition differs between celiac disease (CD) patients and healthy individuals.
- The specific role of gut microbiota in CD pathogenesis remains unclear.
- Early life gut microbiome may influence CD development.
Purpose of the Study:
- To investigate differences in early fecal microbiota composition between infants who later developed CD and healthy controls.
- To assess the association between infant gut microbiota and CD development.
Main Methods:
- 16S rRNA gene sequencing was used to analyze fecal microbiota.
- Stool samples were collected from 27 high-genetic-risk infants at 9 and 12 months of age.
- Microbiota composition was compared between infants who developed CD (n=9) and controls (n=18) by age 4, considering delivery mode, nutrition, and antibiotic use.
Main Results:
- No statistically significant differences in fecal microbiota composition were observed between infants who later developed CD and controls.
- Infant fecal microbiota at 9 and 12 months of age was not associated with CD development.
Conclusions:
- Early fecal microbiota composition does not appear to be a predictor of celiac disease development.
- The study does not rule out potential duodenal microbiota alterations or later microbiota-related triggers for CD.
Objectives:
Several studies have reported that the intestinal microbiota composition of celiac disease (CD) patients differs from healthy individuals. The possible role of gut microbiota in the pathogenesis of the disease is, however, not known. Here, we aimed to assess the possible differences in early fecal microbiota composition between children that later developed CD and healthy controls matched for age, sex and HLA risk genotype.
Materials And Methods:
We used 16S rRNA gene sequencing to examine the fecal microbiota of 27 children with high genetic risk of developing CD. Nine of these children developed the disease by the age of 4 years. Stool samples were collected at the age of 9 and 12 months, before any of the children had developed CD. The fecal microbiota composition of children who later developed the disease was compared with the microbiota of the children who did not have CD or associated autoantibodies at the age of 4 years. Delivery mode, early nutrition, and use of antibiotics were taken into account in the analyses.
Results:
No statistically significant differences in the fecal microbiota composition were found between children who later developed CD (n = 9) and the control children without disease or associated autoantibodies (n = 18).
Conclusions:
Based on our results, the fecal microbiota composition at the age of 9 and 12 months is not associated with the development of CD. Our results, however, do not exclude the possibility of duodenal microbiota changes or a later microbiota-related trigger for the disease.
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