Abdominal pain and functional gastrointestinal disorders in children with celiac disease

Miguel Saps1, Papa Adams, Silvana Bonilla

  • 1Division of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Memorial Hospital, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. msaps@childrensmemorial.org

The Journal of Pediatrics
|October 13, 2012
PubMed

Insights

Children with celiac disease (CD) and healthy controls show similar long-term risks for developing abdominal pain (AP) and related functional gastrointestinal disorders (FGID). Further large prospective studies are recommended to confirm these findings in pediatric populations.

Area of Science:

  • Pediatric Gastroenterology
  • Gastrointestinal Disorders
  • Celiac Disease Research

Background:

  • Celiac disease (CD) is an autoimmune disorder triggered by gluten ingestion.
  • Abdominal pain (AP) and functional gastrointestinal disorders (FGIDs) are common in children.
  • The long-term association between CD and AP/FGIDs requires further investigation.

Purpose of the Study:

  • To determine if children diagnosed with celiac disease have a higher incidence of abdominal pain (AP) and AP-associated functional gastrointestinal disorders (FGIDs) compared to controls.
  • To assess the long-term follow-up of AP and FGIDs in pediatric celiac disease patients.

Main Methods:

  • A retrospective study analyzed data from children (3-22 years) diagnosed with CD between 2000-2010.
  • Parents of CD patients and controls completed a telephone questionnaire and the Questionnaire on Pediatric Gastrointestinal Symptoms-Rome III.
  • Data collection occurred at least 6 months post-CD diagnosis.

Main Results:

  • The study included 49 children with CD and 48 controls.
  • Abdominal pain (AP) was reported by 24.5% of CD patients versus 14.6% of controls (P=.3).
  • AP-associated FGIDs were diagnosed in 18.3% of CD patients compared to 8.3% of controls (P=.23).

Conclusions:

  • Children with celiac disease and control groups exhibited similar risks for developing abdominal pain (AP) and AP-associated FGIDs.
  • Methodological limitations suggest caution in generalizing findings.
  • Large-scale prospective studies are recommended to validate these results.
Abstract

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