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

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

Ngôn ngữ: eng

Ký hiệu phân loại: 005.304 Special topics

Thông tin xuất bản: England : Scientific reports , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 469251

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.
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