Informace o publikaci

Tissue and stool microbiome in pediatric inflammatory bowel disease patients: diversity differs in patients with relapsing and non-relapsing Crohn's disease

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HRALA Matěj DEISSOVÁ Tereza ANDRLA Petr RADOVÁ Lenka ZAHORNACKÁ Saša BOHOŠOVÁ Júlia MACHÁČKOVÁ Táňa KŘEN Leoš HRUNKA Matěj PINKASOVÁ Tereza AMBROZOVÁ Martina BOSÁK Juraj SLABÝ Ondřej ŠMAJS David JABANDŽIEV Petr

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj GUT PATHOGENS
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://link.springer.com/article/10.1186/s13099-025-00766-5?utm_source=getftr&utm_medium=getftr&utm_campaign=getftr_pilot&getft_integrator=clarivate
Doi https://doi.org/10.1186/s13099-025-00766-5
Klíčová slova Pediatric inflammatory bowel disease; Microbiome; Prognostic marker; Barnesiella; Crohn's disease
Přiložené soubory
Popis Background Inflammatory bowel diseases (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are chronic conditions characterized by periods of clinical remission and relapse. Pediatric cases (pIBD) often have a more complicated disease course, where approximately 30% will develop a relapse within a year of diagnosis. Identifying prognostic markers for pIBD is important to optimize treatment and improve long-term outcomes. Our aim was to analyze the tissue microbiome, identify microbial prognostic markers, and validate their predictive power in non-invasive fecal samples. Results Tissue and fecal microbiome were characterized from a prospective cohort comprising 33 therapeutically na & iuml;ve pCD and 23 pUC patients, and 26 non-IBD pediatric controls, using amplicon 16S rRNA gene sequencing. Disease relapse was monitored for one year. At diagnosis, relapsing pCD patients exhibited a significantly decreased alpha diversity and altered beta diversity in tissue compared to non-relapsing pCD patients. Specific taxa were differentially abundant in relapsing pCD, with Barnesiella being the most depleted genus in tissue samples. Receiver Operating Characteristic (ROC) analysis identified Barnesiella (AUC = 0.818), Butyricimonas, and Collinsella as individual microbial tissue markers discriminating pCD relapse. Combining Barnesiella with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI) further enhanced the specificity and sensitivity of the ROC analysis (AUC = 0.872 in tissue, 0.852 in feces), suggesting potential for non-invasive prognostic markers from stool. Conclusions Tissue and fecal microbial markers can predict relapse in pCD patients with high prognostic power, providing a basis for precision medicine and personalized treatment strategies in pIBD.
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