Targeted Analysis of the Gut Microbiome for Diagnosis, Prognosis and Treatment Individualization in Pediatric

Christine Olbjørn1, Milada Cvancarova Småstuen2, Aina Elisabeth Fossum Moen3

  • 1Department for Paediatric and Adolescent Medicine, Akershus University Hospital, NO-1470 Lørenskog, Norway.

Microorganisms
|July 27, 2022
PubMed

Insights

Fecal microbiota analysis in children reveals reduced beneficial bacteria in inflammatory bowel disease (IBD) and non-IBD patients. Bacterial abundance can help diagnose IBD, differentiate Crohn's disease from ulcerative colitis, and predict treatment needs.

Area of Science:

  • Microbiology
  • Pediatric Gastroenterology
  • Gut Microbiome Research

Background:

  • Inflammatory Bowel Disease (IBD) affects children, with Crohn's disease (CD) and ulcerative colitis (UC) being common forms.
  • Understanding the gut microbiome's role in pediatric IBD is crucial for diagnosis and management.
  • Treatment-naïve pediatric IBD patients present unique microbial profiles compared to healthy children.

Purpose of the Study:

  • To investigate fecal microbiota composition in treatment-naïve pediatric IBD patients.
  • To compare microbial profiles between pediatric IBD subtypes (CD and UC) and non-IBD controls.
  • To develop microbial-based indexes for IBD diagnosis, disease phenotype, and prognosis.

Main Methods:

  • Targeted quantitative polymerase chain reaction (qPCR) was used to quantify over 100 bacterial species.
  • Fecal samples were analyzed from pediatric patients with IBD (CD and UC), non-IBD gastrointestinal patients, and healthy children.
  • Diagnostic, Phenotype, and Prognostic Indexes were constructed based on bacterial species abundance.

Main Results:

  • IBD and non-IBD patients showed significantly reduced abundance of beneficial bacterial species compared to healthy children.
  • Crohn's disease patients exhibited lower Bifidobacterium species abundance than ulcerative colitis patients.
  • IBD patients requiring biologic therapy had a lower abundance of butyrate-producing bacteria.
  • High Diagnostic Index correlated with increased odds of having IBD (2.5x).
  • Crohn's disease patients had a higher Phenotype Index than ulcerative colitis patients.
  • High Prognostic Index correlated with increased odds of needing biologic therapy (2.1x).

Conclusions:

  • Fecal bacterial abundance can serve as a biomarker for diagnosing pediatric IBD.
  • Microbiota analysis aids in differentiating between pediatric Crohn's disease and ulcerative colitis.
  • Microbial profiling can identify pediatric IBD patients likely to require biologic therapy.

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