Effect of exclusive enteral nutrition on the microbiota of children with newly diagnosed Crohn's disease

Nadeem O Kaakoush; Andrew S Day; Steven T Leach; Daniel A Lemberg; Shaun Nielsen; Hazel M Mitchell

doi:10.1038/ctg.2014.21

Effect of exclusive enteral nutrition on the microbiota of children with newly diagnosed Crohn's disease

Clin Transl Gastroenterol. 2015 Jan 15;6(1):e71. doi: 10.1038/ctg.2014.21.

Authors

Nadeem O Kaakoush¹, Andrew S Day², Steven T Leach³, Daniel A Lemberg⁴, Shaun Nielsen¹, Hazel M Mitchell¹

Affiliations

¹ School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, Australia.
² 1] Department of Gastroenterology, Sydney Children's Hospital, Sydney, Australia [2] Department of Paediatrics, University of Otago, Christchurch, New Zealand [3] School of Women's and Children's Health, The University of New South Wales, Sydney, Australia.
³ School of Women's and Children's Health, The University of New South Wales, Sydney, Australia.
⁴ Department of Gastroenterology, Sydney Children's Hospital, Sydney, Australia.

Abstract

Objectives: Exclusive enteral nutrition (EEN) is commonly used to treat pediatric Crohn's disease (CD). Meta-analysis of pediatric studies that have compared the effect of EEN with other treatments have shown that EEN induces remission in up to 80-85% of patients. We aimed to gain a comprehensive understanding of the effect of EEN on the microbiota of CD patients.

Methods: We used 16S rRNA gene and whole-genome high throughout sequencing to determine changes in the fecal microbiota of five CD children, before, during, and after EEN therapy and compared this with five healthy controls.

Results: The microbial diversity observed in CD patients tended to be lower than that in controls (CD: 2.25±0.24, controls: 2.75±0.14, P=0.11). In all CD patients, dysbiosis was observed prior to therapy. EEN therapy had a positive effect in all patients, with 80% going into remission. In some patients, the positive effect diminished following the conclusion of EEN therapy. Significantly, the number of operational taxonomic units (OTU) decreased dramatically upon starting EEN and this corresponded with CD remission. Recurrence of CD corresponded with an increase in OTUs. Six families within the Firmicutes were found to correlate with disease activity during and following EEN therapy, a finding that was confirmed by whole-genome high throughput sequencing.

Conclusions: Our results demonstrate that EEN leads to common and patient-specific alterations in the microbiota of CD patients, a number of which correlate with disease activity.