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Randomized Controlled Trial
. 2022 Dec 14;28(46):6589-6598.
doi: 10.3748/wjg.v28.i46.6589.

Prevalence of functional gastrointestinal disorders in children with celiac disease on different types of gluten-free diets

Affiliations
Randomized Controlled Trial

Prevalence of functional gastrointestinal disorders in children with celiac disease on different types of gluten-free diets

Francesca Fiori Nastro et al. World J Gastroenterol. .

Abstract

Background: Functional gastrointestinal disorders (FGIDs) are common during the pediatric age. FGIDs are not related to biochemical or structural abnormalities. However, since they have a high prevalence, several studies have evaluated an overlap between FGIDs and organic diseases. Individuals with celiac disease (CD) have been shown to be at an increased risk for functional abdominal pain, even if they adhere well to a gluten-free diet (GFD). Little information is available for the pediatric age group. The aims of our study were to evaluate the prevalence of FGIDS in CD children 1 year after diagnosis and to compare the prevalence of FGIDs in CD children on a GFD with processed foods compared with those on a GFD with natural products.

Aim: To assess the prevalence of FGIDs in children with CD after 1 year of follow-up and to compare the prevalence of FGIDs in children with CD on a GFD with processed foods and in children on a GFD with natural products.

Methods: We recruited pediatric patients aged 1-18 years with a new CD diagnosis. Participants were randomized to two groups: Group A on a GFD with processed foods (diet 1); and group B on a GFD with natural products (diet 2). Clinical monitoring, diet assessment and the questionnaire on pediatric gastrointestinal symptoms-Rome IV version were performed at diagnosis (T0) and after 12 mo of follow-up (T1). Dietary intake was assessed using a 3-d food diary record. Data from the diaries were evaluated using WinFood nutrient analysis software. We assessed the prevalence of FGIDs at T1 and the correlation with the type of GFD.

Results: We registered 104 CD children, with 55 patients in group A (53.0%) and 49 patients in group B (47.0%). Initially, 30 of the 55 (54.5%) CD children were symptomatic in group A, while 25 of 49 (51.0%) were symptomatic in group B. At T1, in spite of a low or negative serology for CD, FGIDs prevalence was 10/55 (18.0%) in group A and 8/49 (16.3%) in group B, with no statistically significant difference between the two groups (P = 0.780). At T1 the macro- and micronutrient intake was similar across the two groups with no significant differences in nutrient analysis. However, in both groups at T1 we found that a lower prevalence of FGIDs (P = 0.055) was associated with an inferior caloric (odds ratio = 0.99, 95% confidence interval: 0.99-1.00) and fat (odds ratio = 0.33, 95% confidence interval: 0.65-0.95) intake.

Conclusion: Our results showed that CD children on a GFD have gastrointestinal symptoms with an elevated prevalence of FGIDs. Our study suggests that developing FGIDs may be linked to caloric intake and percentage of food fat, but it does not change between a GFD with processed foods or a GFD with natural products. However, long-term monitoring is required to evaluate a correlation between FGIDs and various types of GFDs.

Keywords: Celiac disease; Children; Functional gastrointestinal disorders; Gastrointestinal symptoms; Gluten free diet.

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Conflict of interest statement

Conflict-of-interest statement: All authors report no relevant conflicts of interest for this article.

Figures

Figure 1
Figure 1
Prevalence of functional gastrointestinal disorders in children affected by celiac disease at diagnosis and after 1 year of follow-up in group A (consumed a gluten-free diet with processed foods) and group B (consumed a gluten-free diet with natural foods). T0 was the time at the initial diagnosis of celiac disease. T1 was the time at the 1-year follow-up after diagnosis of celiac disease. GA: Group A; GB: Group B.
Figure 2
Figure 2
Decreased fat and calorie intake was correlated with disease persistence of functional gastrointestinal disorders after 1 year of follow-up.

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