The intestinal microbiome of inflammatory bowel disease across the pediatric age range

• Published in: Gut microbes Vol. 16; no. 1; p. 2317932
• Main Authors: Conrad, Máire A, Bittinger, Kyle, Ren, Yue, Kachelries, Kelly, Vales, Jennifer, Li, Hongzhe, Wu, Gary D, Bushman, Frederic D, Devoto, Marcella, Baldassano, Robert N, Kelsen, Judith R
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 2024; Taylor & Francis Group
• Subjects: Adult; Child; Dysbiosis; Gastrointestinal Microbiome; gut microbiome; Humans; Infant; Inflammation; Inflammatory bowel disease; Inflammatory Bowel Diseases - epidemiology; intestinal microbiome; Microbiota; pediatrics; Research Paper; very early onset inflammatory bowel disease; Inflammatory bowel disease; gut microbiome; microbial maturity; very early onset inflammatory bowel disease; pediatrics; intestinal microbiome; dysbiosis
• ISSN: 1949-0976; 1949-0984; 1949-0984
• DOI: 10.1080/19490976.2024.2317932

Dysbiosis is associated with pediatric and adult-onset inflammatory bowel disease (IBD), but the role of dysbiosis and the microbiome in very early onset IBD (VEO-IBD) has not yet been described. Here, we aimed to demonstrate the impact of age and inflammation on microbial community structure using shotgun metagenomic sequencing in children with VEO-IBD, pediatric-onset IBD, and age-matched pediatric healthy controls (HC) observed longitudinally over the course of 8 weeks. We found disease-related differences in alpha and beta diversity between HC and children with IBD or VEO-IBD. Using a healthy microbial maturity index modeled from HC across the age range to characterize their gut microbiota, we found that children with pediatric-onset IBD and VEO-IBD had lower maturity than their age-matched HC groups, suggesting a disease effect on the microbial community. In addition, patients with pediatric IBD had significantly lower maturity than those with VEO-IBD, who had more heterogeneity at the youngest ages, highlighting differences in these two cohorts that were not captured in standard comparisons of alpha and beta diversity. These results demonstrate that young age and inflammation independently impact microbial community structure. However, the effect is not additive in the youngest patients, likely because of the heterogeneous and dynamic stool microbiome in this population.