Age-Dependent Trends in the Celiac Disease: A Tertiary Center Experience

Alexander Krauthammer1,2, Anat Guz-Mark1,2, Noam Zevit1,2

  • 1Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center of Israel.

Insights

Younger children with celiac disease (CD) often show malabsorption symptoms and higher antibody levels, but improve faster on a gluten-free diet (GFD). Awareness of these age-dependent patterns is crucial for diagnosis and management.

Area of Science:

  • Pediatric Gastroenterology
  • Autoimmune Disorders
  • Clinical Research

Background:

  • Celiac disease (CD) is a common intestinal autoimmune disorder with varied clinical presentations.
  • Understanding age-specific patterns in CD is essential for accurate diagnosis and effective management.

Purpose of the Study:

  • To investigate age-dependent variations in the presentation, diagnosis, and management of celiac disease in pediatric patients.
  • To compare clinical and laboratory features of CD across different pediatric age groups.

Main Methods:

  • Retrospective review of electronic medical records for 932 pediatric patients diagnosed with CD.
  • Patients were categorized into four age groups at diagnosis: 0-3, 3-6, 6-12, and 12-18 years.
  • Demographic, clinical, and laboratory parameters were compared across the age groups.

Main Results:

  • Younger children (0-3 years) more frequently exhibited diarrhea, weight loss, vomiting, abdominal distention, lower weight z-scores, hypoalbuminemia, and zinc deficiency.
  • Anemia rates were higher in younger age groups (0-3 and 3-6 years).
  • Patients aged 0-6 years more often presented with tissue transglutaminase (TTG) levels >10x ULN and normalized CD serologies faster on a gluten-free diet (GFD).

Conclusions:

  • Celiac disease presentation and course in children vary significantly with age.
  • Younger pediatric patients typically present with more pronounced malabsorptive symptoms and higher TTG levels.
  • Faster serological normalization on GFD in younger children suggests distinct disease dynamics that clinicians should recognize.
Abstract