Related Experiment Video
Updated: Jul 15, 2026

Chronic Salmonella Infection Induced Intestinal Fibrosis
Published on: September 22, 2019
Inflammatory bowel disease in children: a pediatrician's perspective
1Division of Pediatric Gastroenterology, The Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. ccuffari@jhmi.edu
Insights
Genetics, particularly NOD2/CARD15 mutations, influence pediatric Crohn's disease (CD) risk and presentation. Early immunomodulator use and novel therapies show promise for managing pediatric inflammatory bowel disease (IBD).
Area of Science:
- Pediatric Gastroenterology
- Genetics of Inflammatory Bowel Disease (IBD)
- Pharmacogenomics
Background:
- Crohn's disease (CD) and ulcerative colitis (UC) are chronic, heterogeneous inflammatory bowel disorders affecting children, comprising up to 25% of IBD cases.
- Genetic factors, including NOD2/CARD15 gene mutations, are implicated in pediatric CD, particularly in small bowel disease and early onset.
- Distinguishing between CD and UC in children remains challenging, even with advanced diagnostics, with subclinical disease identifiable by growth velocity changes.
Purpose of the Study:
- To explore the genetic underpinnings of pediatric Crohn's disease, focusing on NOD2/CARD15 mutations.
- To review diagnostic challenges and advancements in pediatric inflammatory bowel disease.
- To discuss current and novel therapeutic strategies for managing pediatric IBD.
Main Methods:
- Review of existing literature on pediatric inflammatory bowel disease genetics, diagnosis, and treatment.
- Analysis of the role of NOD2/CARD15 mutations in Crohn's disease etiology and phenotype.
- Evaluation of the efficacy of immunomodulators and emerging treatments like infliximab in pediatric IBD.
Main Results:
- NOD2/CARD15 mutations are associated with increased risk and specific disease patterns (e.g., stricturing small bowel disease) in pediatric CD.
- Early introduction of immunomodulators like azathioprine and 6-mercaptopurine is effective for long-term remission in pediatric IBD.
- Pharmacogenomic analysis of 6-mercaptopurine metabolism aids in predicting toxicity and personalizing therapy.
Conclusions:
- Genetic predisposition plays a significant role in pediatric Crohn's disease.
- Effective management of pediatric IBD involves early immunomodulatory therapy and consideration of pharmacogenomics.
- Ongoing research into novel treatments aims to improve efficacy and reduce the need for surgery in pediatric IBD patients.
Abstract:
Crohn's disease (CD) and ulcerative colitis (UC) are common and heterogeneous chronic inflammatory bowel disorders of childhood that account for up to 25% of all patients with inflammatory bowel disease (IBD). In CD, the familial pattern of disease concordance would suggest that genetics contribute to disease etiology. Children are more likely to have proximal small bowel disease complicated by stricture formation, fistulization and the need for surgical intervention. The predisposition for small bowel disease has been associated with mutations of the nucleotide oligomerization domain 2 (NOD2)/Caspase activation and recruitment domain 15 (CARD15) gene on chromosome 16 in 1/3 of patients with CD. Homozygous patients also show an early age at disease onset and a relatively high relative risk for isolated stricturing distal ileal disease. The potential clinical role for NOD2 testing in either the diagnosis or the therapeutic management of patients with CD has yet to be determined. The precise age of onset of CD and UC can be difficult in children. Subclinical phases of disease can be identified through a decrease in weight and height velocity, and a delay in pubertal development. However, a confident distinction between CD and UC also remains a taxonomic dilemma in 25% of pediatric patients with IBD, despite recent technological advances in diagnostic techniques, including gadolinium enhanced magnetic resonance imaging (MRI) and capsule endoscopy, and serological testing. The early introduction of immunomodulators, including azathioprine and 6-mercaptopurine have proven efficacy in maintaining long-term remission without concurrent corticosteroids. The pharmacogenomic of 6-MP metabolism has been shown to be useful in predicting susceptibility to antimetabolite induced toxicity, and possibly allowing physician's to individualize drug therapy to improve clinical response. Novel treatment strategies, including infliximab are being developed in Pediatrics with the aim at improving overall treatment efficacy and potentially avoid surgery.
Related Concept Videos
Inflammatory Bowel Disease I: Ulcerative Colitis
Inflammatory bowel disease, or IBD, encompasses a group of disorders characterized by chronic inflammation or ulceration of the gastrointestinal tract.
Risk Factors
The exact cause of IBD remains unclear, although it is believed to be due to a mix of genetic, environmental, microbial, and immune factors. Genetic factors are significant in determining susceptibility to IBD, with family history being a critical risk factor. Individuals with a first-degree relative who has IBD are at...
Inflammatory Bowel Disease II: Crohn's Disease
Inflammatory bowel disease, commonly known as IBD, refers to a collection of disorders that lead to persistent inflammation of the gastrointestinal tract. The two types of IBD are ulcerative colitis, which impacts the colon, and Crohn's disease, which can involve any part of the gastrointestinal segment.
Crohn's disease
Crohn's disease is a chronic, systemic inflammatory bowel disease (IBD) that predominantly affects the gastrointestinal tract. It is marked by transmural...
Inflammatory Bowel Disease III: Diagnostic Studies and Management I-Nutritional Therapy
Diagnostic studies
A colonoscopy is the definitive screening test, distinguishing ulcerative colitis from other colon diseases with similar symptoms. During a colonoscopy test, inflamed mucosa with exudate ulcerations can be observed, and biopsies are taken to determine the histologic characteristics of the colonic...
Inflammatory Bowel Disease I: Introduction
Inflammatory Bowel Disease III: Crohn's Disease
Inflammatory Bowel Disease IV: Clinical Manifestations

