失调
微生物群
炎症性肠病
疾病
基因组
生物
免疫学
发病年龄
人口
医学
内科学
生物信息学
环境卫生
遗传学
基因
作者
Máire A. Conrad,Kyle Bittinger,Yue Ren,Kelly Kachelries,J.M. Guerra Vales,Hongzhe Li,Gary D. Wu,Frederic D. Bushman,Marcella Devoto,Robert N. Baldassano,Judith R. Kelsen
出处
期刊:Gut microbes
[Landes Bioscience]
日期:2024-02-25
卷期号:16 (1)
被引量:4
标识
DOI:10.1080/19490976.2024.2317932
摘要
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.
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