Faecal Metabolomics in Paediatric Inflammatory Bowel Disease: A Systematic Review

Author:

Jagt Jasmijn Z12ORCID,Verburgt Charlotte M345ORCID,de Vries Ralph6ORCID,de Boer Nanne K H7,Benninga Marc A3,de Jonge Wouter J48,van Limbergen Johan E349,de Meij Tim G J13

Affiliation:

1. Department of Paediatric Gastroenterology, Emma Children’s Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam , HV Amsterdam , The Netherlands

2. Amsterdam UMC, Vrije Universiteit Amsterdam, Paediatric Gastroenterology, Amsterdam Gastroenterology Endocrinology Metabolism , De Boelelaan, Amsterdam , Netherlands

3. Department of Paediatric Gastroenterology and Nutrition, Amsterdam University Medical Centres – location University of Amsterdam, Emma Children’s Hospital , AZ Amsterdam , The Netherlands

4. Tytgat Institute for Liver and Intestinal Research, Amsterdam Gastroenterology Endocrinology Metabolism, University of Amsterdam , BK Amsterdam , The Netherlands

5. Amsterdam Reproduction & Development , AZ Amsterdam , The Netherlands

6. Medical Library, Vrije Universiteit Amsterdam , HV Amsterdam , The Netherlands

7. Department of Gastroenterology and Hepatology, Amsterdam Gastroenterology and Metabolism Research Institute (AGEM), Amsterdam University Medical Centre, Vrije Universiteit Amsterdam , Amsterdam , The Netherlands

8. Department of Surgery, University of Bonn , Bonn , Germany

9. Department of Pediatrics, Dalhousie University , Halifax, NS , Canada

Abstract

Abstract Background and Aims Paediatric inflammatory bowel disease [IBD] is characterized by altered immunological and metabolic pathways. Metabolomics may therefore increase pathophysiological understanding and could develop into characterization of biomarkers for diagnosis and IBD treatment response. However, no uniform metabolomic profiles have been identified to date. This systematic review aimed to identify faecal metabolomic signatures in paediatric IBD vs controls, and to describe metabolites associated with disease activity and treatment response. Methods A literature search was performed in Embase, Medline, Web of Science and Cochrane Library. Studies assessing faecal metabolomics in paediatric patients < 18 years with IBD [de novo, active, inactive] with comparative groups [IBD vs non-IBD; responders vs non-responders] were included. The quality of included studies was assessed according to the Newcastle–Ottawa Scale. Results Nineteen studies were included [540 patients with IBD, 386 controls], assessing faecal short-chain fatty acids [SCFA] [five studies], amino acids [AA] [ten studies], bile acids [BA] [eight studies] and other metabolites [nine studies] using various methodologies. Significantly increased levels of AA [particularly phenylalanine], primary BA and lower levels of secondary BA were described in paediatric IBD compared to controls. Faecal SCFA results varied across studies. Additionally, responders and non-responders to exclusive enteral nutrition and infliximab showed differences in baseline faecal metabolites [based on BA, AA]. Conclusions This systematic review provides evidence for distinct faecal metabolomic profiles in paediatric IBD. However, results varied across studies, possibly due to differences in study design and applied analytical techniques. Faecal metabolomics could provide more insight into host–microbial interactions in IBD, but further studies with standardized methodologies and reporting are needed.

Funder

Maag Lever Darm Stichting

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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