Original Article
Abdominal Pain and Functional Gastrointestinal Disorders in Children with Celiac Disease

https://doi.org/10.1016/j.jpeds.2012.08.032Get rights and content

Objective

To assess whether patients with celiac disease (CD) are more likely than controls to develop abdominal pain (AP) and AP-associated functional gastrointestinal disorders (FGID) in long-term follow-up.

Study design

In a retrospective study, data on children (3-22 years old) with CD diagnosed between 2000 and 2010 were obtained. Parents were contacted by telephone at least 6 months after the diagnosis of CD and invited to participate in the study. Consenting parents completed: (1) a telephone questionnaire on the presence of gastrointestinal symptoms; and (2) the parent report version of the Questionnaire on Pediatric Gastrointestinal Symptoms-Rome III for cases and selected controls.

Results

Forty-nine cases (mean 11.3 years, 20 male participants) and 48 controls (mean 11.1 years, 24 male participants) were enrolled. Twelve children in the CD group (24.5%) and 7 children in the control group (14.6%) had AP at the time of the study (P = .3). Nine children in the CD group (18.3%) and 4 children in the control group (8.3%) met criteria for an AP-associated FGID according to the Questionnaire on Pediatric Gastrointestinal Symptoms-Rome III (P = .23).

Conclusion

It was found that children with CD and controls have a similar risk of AP and AP-FGIDs. Methodologic limitations prevent generalization of results, but large prospective studies should confirm the findings.

Section snippets

Methods

Data on children (3-22 years old) with CD diagnosed at Children's Memorial Hospital between 2000 and 2010 were obtained. Charts were reviewed and the pathologic diagnosis of CD was confirmed in all cases. Children who had a wrong diagnosis or developmental delay and those from non–English-speaking families were excluded. Parents were contacted by telephone at least 6 months following the diagnosis of CD and invited to participate in the study. Consenting parents completed: (1) a telephone

Results

Forty-six families participated in the study (43 families had 1 child with CD and 3 families had 2 children with CD). Forty-nine cases (mean 11.3 years, 20 male participants) and 48 controls (mean 11.1 years, 24 male participants) were enrolled; 43 of the 49 children with CD had at least 1 sibling who was included as a control in the study (Figure). For 16 patients who lacked a sibling control, a second sibling was recruited in 13 cases and a cousin in 2 cases. Twenty-two patients who were

Discussion

This study assessed the long-term risk of AP in children with CD. The focus of our study differs from that of most studies. Although most studies have focused on the possible relation between CD and FGIDs at the time of diagnosis, we were interested in the long-term relation among CD, AP, and AP-FGIDs. Previous studies on various gastrointestinal inflammatory conditions have consistently found that children with gastrointestinal inflammation were at risk of developing AP and AP-FGIDs. Children

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      With the assumption that IBS would be expected in 4.2% of the general Italian pediatric population17 and in 7.3% of CD patients,18 we calculated that a sample of 371 children with CD would be required for the study to have 80% power based on a 2-sided type 1 error rate of 5%. This sample size has a 95% power based on a 2-sided type 1 error rate of 1% to identify a difference in the prevalence of FAPD in CD patients vs controls considering a prevalence of FAPD in 9% of controls17 and in 18% of CD patients.18–20 Risk models were developed using a decisional tree.

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      2017, Journal of Pediatrics
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      For the purpose of this study, children who had 2 months of AP as required by the Rome III criteria for the diagnosis of an AP-FGID but did not meet the frequency of symptoms required in the criteria were given a diagnosis of chronic AP. Our previous study of CD and siblings with AP-FGID required a sample size of 44 subjects per group to demonstrate a significant difference between 2 groups (CD vs each control group) based on a power of 80% and an alpha of 0.05.25 The sample size for this study was doubled empirically to improve the power of the study.

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    The authors declare no conflicts of interest.

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