4.5 Article

Decline in Presumptively Protective Gut Bacterial Species and Metabolites Are Paradoxically Associated with Disease Improvement in Pediatric Crohn's Disease During Enteral Nutrition

期刊

INFLAMMATORY BOWEL DISEASES
卷 20, 期 5, 页码 861-871

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MIB.0000000000000023

关键词

short-chain fatty acids; enteral nutrition; Crohn's disease; pediatrics; gut microbiota

资金

  1. Greek State Scholarship Foundation
  2. Hellenic Foundation of Gastroenterology, and Nutrition
  3. Barr Endowment Fund
  4. Yorkhill Children's Foundation
  5. Medical Research Council patient research cohorts initiative grant [G0800675]
  6. NHS Research Scotland career fellowship award
  7. Catherine McEwan Foundation
  8. Yorkhill IBD fund
  9. Crohn's in Childhood Research Association (CICRA)
  10. MSD Immunology
  11. Abbott
  12. Dr Falk
  13. Nestle
  14. Ferring Pharmaceuticals
  15. Falk
  16. ILSI Europe
  17. Foods Standards Agency
  18. Warner Chillcott
  19. MSD
  20. Ferring
  21. MRC [G0800675] Funding Source: UKRI
  22. Medical Research Council [G0800675] Funding Source: researchfish
  23. Medical Research Foundation [C0482] Funding Source: researchfish

向作者/读者索取更多资源

Background: The gut microbiota is implicated in the pathogenesis of Crohn's disease (CD). Exclusive enteral nutrition (EEN) is a successful treatment, but its mode of action remains unknown. This study assessed serial changes in the fecal microbiota milieu during EEN. Methods: Five fecal samples were collected from CD children: 4 during EEN (start, 15, 30, end EEN approximately 60 days) and the fifth on habitual diet. Two samples were collected from healthy control subjects. Fecal pH, bacterial metabolites, global microbial diversity abundance, composition stability, and quantitative changes of total and 7 major bacterial groups previously implicated in CD were measured. Results: Overall, 68 samples were from 15 CD children and 40 from 21 control subjects. Fecal pH and total sulfide increased and butyric acid decreased during EEN (all P < 0.05). Global bacterial diversity abundance decreased (P < 0.05); a higher degree of microbiota composition stability was seen in control subjects than in CD children during EEN (at P <= 0.008). Faecalibacterium prausnitzii spp concentration significantly decreased after 30 days on EEN (P < 0.05). In patients who responded to EEN, the magnitude of the observed changes was greater and the concentration of Bacteroides/Prevotella group decreased (P < 0.05). All these changes reverted to pretreatment levels on free diet, and EEN microbiota diversity increased when the children returned to their free diet. Conclusions: EEN impacts on gut microbiota composition and changes fecal metabolic activity. It is difficult to infer a causative association between such changes and disease improvement, but the results do challenge the current perception of a protective role for F. prausnitzii in CD.

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