Fecal microbiota and genetics in pediatric-onset orofacial granulomatosis and Crohn´s disease

Miikka Höyhtyä, Anu Haaramo, Anne Nikkonen, Rebecka Ventin-Holmberg, Nitin Agrawal, Jarmo Ritari, Brandon Hickman, Jukka Partanen, Heikki Alapulli, Jetta Tuokkola, Anne Salonen, Willem M. de Vos, Kaija Leena Kolho*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Orofacial granulomatosis (OFG) is a rare chronic inflammatory condition. It is under debate, whether it is a condition of its own or merely a subtype of Crohn's disease (CD). We aimed to search for markers characteristic of patients with pediatric-onset OFG compared to patients with pediatric-onset CD. We recruited young patients with OFG (with or without CD, n = 29), CD (n = 24), and healthy controls (n = 20). All participants provided a fecal sample for microbiota and calprotectin analyses and saliva for DNA analysis of genes associated with OFG and kept a 3-day food diary. Oral disease activity was evaluated using The Oral Disease Activity Score by an otorhinolaryngologist and a dentist. We observed decreased relative abundance in class Clostridia and increased relative abundances of classes Actinobacteria and Bacilli in the feces of patients with OFG when compared to patients with CD and healthy controls. The relative abundances of Bifidobacterium adolescentis increased and Faecalibacterium prausnitzii decreased along with the increase in the Oral Disease Activity Score. We found the NOD2 gene rs8057341 allele A to be enriched in patients with OFG compared to patients with CD. These findings support the theory that OFG is a distinct disease phenotype.

Original languageEnglish
Article number6020
Number of pages9
JournalScientific Reports
Volume15
DOIs
Publication statusPublished - 19 Feb 2025

Keywords

  • Children
  • Genotype
  • Inflammatory bowel diseases
  • Oral

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