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Clinical and Paraclinical Screening for Celiac Disease in Children with Intractable Epilepsy
Golnaz Ghazizadeh Esslami1, Bahar Allahverdi2, Reza Shervin Badv3
1Department of Pediatrics, Ziaeian Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Insights
This study found no evidence of celiac disease in children with intractable epilepsy. Gastrointestinal issues and growth problems in these children are likely due to other causes, not gluten sensitivity.
Area of Science:
- Pediatric Neurology
- Gastroenterology
- Immunology
Background:
- Celiac disease is an autoimmune disorder triggered by gluten in susceptible individuals.
- Previous research suggests a potential link between celiac disease and epilepsy in pediatric populations.
- This study investigated celiac disease prevalence in children with refractory epilepsy.
Purpose of the Study:
- To screen for clinical and paraclinical indicators of celiac disease in children experiencing intractable epilepsy.
- To determine if gluten hypersensitivity contributes to epilepsy in this demographic.
Main Methods:
- A cross-sectional study enrolled 70 children (ages 2-18) with drug-resistant epilepsy.
- Data collected included demographics, clinical features, and gastrointestinal symptoms.
- Serological tests for celiac disease (IgA, anti-tTG, anti-endomysial antibody) were performed; endoscopy was reserved for positive cases.
Main Results:
- No children tested positive for celiac disease antibodies.
- Consequently, no endoscopic examinations or biopsies were conducted.
- Common symptoms included constipation (48.6%), anorexia (25.7%), and abdominal pain (21.4%), alongside growth deficiencies.
Conclusions:
- Celiac disease was not identified as a comorbidity in children with intractable epilepsy.
- Observed gastrointestinal symptoms and growth issues are more likely attributable to the underlying epilepsy or its treatments rather than celiac disease.
Background:
Celiac disease is the inflammatory entropy caused by hypersensitivity to gluten, which occurs in susceptible individuals. Some studies have suggested a link between celiac disease and epilepsy in children. Our aim was to screen for clinical and paraclinical features of celiac disease in children with intractable epilepsy.
Methods:
This was a cross-sectional study. Children aged 2 to 18 years with refractory epilepsy that referred to the pediatric neurology clinic within one year (2018-2019) were enrolled. Demographic and clinical characteristics of patients, especially clinical manifestations of celiac disease, were recorded in a questionnaire. A venous blood sample was sent to determine the total IgA, anti-tTG (IgA), and anti-endomysial antibody (IgA). Endoscopy was performed in cases where the celiac serological test was positive.
Results:
Seventy children with idiopathic drug-resistant epilepsy (44 boys) were evaluated. The height-for-age index was 49.2% and the weight-for-age index was 38.2% less than normal. Constipation (48.6%), anorexia (25.7%), and abdominal pain (21.4%) were the most common gastrointestinal symptoms. Celiac serological tests were negative in all children. Therefore, endoscopy and bowel biopsy were not performed in any case.
Conclusion:
Celiac disease was not found in any patient with intractable epilepsy. Gastrointestinal symptoms and growth disorders in this group may be related to the underlying disease or medications and not to celiac disease.
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