Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Gut Microbes. 2024 Jan-Dec;16(1):2317932. doi: 10.1080/19490976.2024.2317932. Epub 2024 Feb 25.
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.
肠道菌群失调与儿童和成人发病的炎症性肠病(IBD)有关,但肠道菌群失调和微生物组在非常早发的 IBD(VEO-IBD)中的作用尚未描述。在这里,我们旨在通过对 VEO-IBD、儿科发病 IBD 患儿和年龄匹配的儿科健康对照者(HC)进行纵向 8 周的研究,利用宏基因组测序展示年龄和炎症对微生物群落结构的影响。我们发现 HC 与 IBD 或 VEO-IBD 患儿之间在 alpha 和 beta 多样性方面存在疾病相关差异。使用 HC 在整个年龄段建立的健康微生物成熟度指数来描述其肠道微生物群,我们发现儿科发病 IBD 和 VEO-IBD 患儿的成熟度低于其年龄匹配的 HC 组,表明疾病对微生物群落有影响。此外,儿科 IBD 患者的成熟度明显低于 VEO-IBD 患者,后者在最小年龄时具有更高的异质性,突出了这两个队列之间的差异,这些差异无法通过 alpha 和 beta 多样性的标准比较来捕捉。这些结果表明,年轻年龄和炎症独立影响微生物群落结构。然而,在最小的患者中,这种影响不是相加的,这可能是由于该人群的粪便微生物组具有异质性和动态性。