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Increased prevalence of silent celiac disease among Greek epileptic children
Antigoni Mavroudi1, Mavroudi Antigoni, Ioannis Xinias
13rd Pediatric Clinic, Aristotle University of Thessaloniki Medical School, Hippocration Hospital, Thessaloniki, Greece.
Insights
Silent celiac disease is more common in children with epilepsy. Testing for tissue transglutaminase IgA antibodies is a good screening method for celiac disease in these patients.
Area of Science:
- Pediatric Neurology
- Gastroenterology
- Immunology
Background:
- Celiac disease is an immune-mediated enteropathy linked to gluten intake in susceptible individuals.
- Associations between epilepsy, celiac disease, and intracranial calcifications have been reported.
- The prevalence of silent celiac disease in pediatric epilepsy requires further investigation.
Purpose of the Study:
- To investigate the prevalence of celiac disease in children with idiopathic epilepsy.
- To evaluate the diagnostic utility of specific antibody markers for celiac disease in this population.
- To determine the association between celiac disease and intracranial calcifications in epileptic children.
Main Methods:
- Screening 255 children with idiopathic epilepsy for various celiac disease antibodies (IgA, IgG antigliadin, IgA antitissue transglutaminase, IgA antiendomysial, antireticulin).
- Performing small intestinal biopsies in patients with positive IgA antigliadin antibodies.
- Comparing findings with 280 healthy control children.
Main Results:
- Five epileptic children showed intestinal histopathologic changes and/or positive celiac disease antibodies, not observed in controls (P = 0.0241).
- No intracranial calcifications were found in epileptic children diagnosed with celiac disease.
- The study identified an increased prevalence of silent celiac disease in children with idiopathic epilepsy.
Conclusions:
- Silent celiac disease is more prevalent in children with idiopathic epilepsy, irrespective of epilepsy type.
- Serum IgA antitissue transglutaminase antibodies show promise as a reliable screening marker for celiac disease.
- Occipital corticosubcortical calcifications appear to be less common in pediatric epilepsy patients with celiac disease.
Abstract:
Celiac disease is an immune-mediated enteropathy triggered by the ingestion of gluten in genetically susceptible individuals. Many reports mention the association between epilepsy and celiac disease and the occasional presence of occipital corticosubcortical calcifications. We investigated 255 children with idiopathic epilepsy. Evaluation included use of routine, easily obtainable studies. Patients were screened for immunoglobulin A (IgA), immunoglobulin G (IgG) antigliadin antibodies and immunoglobulin A antitissue transglutaminase antibodies. Moreover, presence of IgA antiendomysial and antireticulin antibodies was screened. Patients with positive IgA antigliadin antibodies underwent a small intestinal biopsy. Controls consisted of 280 healthy children. Intestinal histopathologic changes, positive IgA antigliadin antibodies or IgG antigliadin antibodies, antireticulin antibodies, and antitissue transglutaminase IgA antibodies were found in five epileptic children but not in control subjects (P = 0.0241). Intracranial calcifications were not found in epileptic children with celiac disease. The findings indicate that prevalence of silent celiac disease is increased among children with idiopathic epilepsy; the type of epilepsy does not appear to play a role. Serum antitissue transglutaminase IgA antibodies could be a good marker for celiac disease screening. Occipital corticosubcortical calcifications are rarer in children with celiac disease and epilepsy.
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