Fecal Amino Acid Analysis Can Discriminate De Novo Treatment-Naïve Pediatric Inflammatory Bowel Disease From Controls

Sofie Bosch, Eduard A Struys, Nora van Gaal, Abdellatif Bakkali, Erwin W Jansen, Kay Diederen, Marc A Benninga, Chris J Mulder, Nanne K H de Boer, Tim G J de Meij

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

OBJECTIVES: Endoscopy remains mandatory in the diagnostic work-up of inflammatory bowel disease (IBD), but is a costly and invasive procedure. Identification of novel, non-invasive, diagnostic biomarkers remains a priority. The aim of this study was to explore the potential of fecal amino acid composition as diagnostic biomarker for pediatric IBD.

METHODS: In this case-control study, treatment-naïve, de novo pediatric IBD patients from two tertiary centers were included. Endoscopic severity of ulcerative colitis (UC) and Crohn's disease (CD) was based on global physician assessment scores, substantiated by levels of fecal calprotectin and C-reactive protein at study inclusion. Patients were instructed to collect a fecal sample prior to bowel cleansing. Healthy controls were recruited from primary schools in the same region. Dedicated amino acid analysis was performed on all samples.

RESULTS: Significant differences between 30 IBD patients (15 UC, 15 CD) and 15 age and sex matched healthy controls (HC) were found in six amino acids (histidine, tryptophan, phenylalanine, leucine, tyrosine and valine; all AUC > 0.75 and p < 0.005), displaying higher levels in IBD. When distributing the patients according to type of IBD, a similar spectrum of amino acids differed between UC and HC (histidine, tryptophan, phenylalanine, leucine, valine and serine), whereas three amino acids were different between CD and HC (histidine, tryptophan and phenylalanine).

CONCLUSION: Significantly increased levels of six different fecal amino acids were found in IBD patients compared to controls. Whether these differences reflect decreased absorption or increased loss by inflamed intestines needs to be elucidated.

Original languageEnglish
Pages (from-to)773-778
Number of pages6
JournalJournal of Pediatric Gastroenterology and Nutrition
Early online date3 Nov 2017
DOIs
Publication statusPublished - 1 May 2018

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