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Increased risk for coeliac disease in paediatric patients with migraine
1Divisions of Child Neurology, Baskent University of Medicine, Ankara, Turkey. falehan@hotmail.com
Insights
This study found a higher prevalence of coeliac disease (CD) markers in children with migraine. These findings suggest a potential link between paediatric migraine and CD.
Area of Science:
- Neurology
- Gastroenterology
- Immunology
Background:
- Migraine is a common neurological disorder in children.
- Coeliac disease (CD) is an autoimmune disorder triggered by gluten.
- The association between paediatric migraine and CD requires further investigation.
Purpose of the Study:
- To investigate the prevalence of coeliac disease (CD) in paediatric patients experiencing migraine.
- To assess the presence of serum tissue transglutaminase IgA (tTGA) antibodies in children with migraine.
Main Methods:
- Serum tTGA antibody and IgA levels were measured in 73 paediatric migraine patients and 147 controls.
- Patients with positive tTGA antibodies underwent duodenal biopsy for histological confirmation.
- Prevalence rates were compared between the study and control groups.
Main Results:
- Four (5.5%) paediatric migraine patients and one (0.6%) control subject had positive tTGA antibody titres (P < 0.05).
- Three migraine patients with positive tTGA antibodies showed normal duodenal histology, indicating potential CD.
- One patient in each group declined biopsy.
Conclusions:
- A higher prevalence of tTGA antibodies was observed in paediatric migraine patients compared to controls.
- The findings suggest a potential association between migraine and coeliac disease in children.
- Further research is warranted to elucidate the relationship between these conditions.
Abstract:
The aim was to determine the prevalence of coeliac disease (CD) in paediatric patients with migraine. Serum tissue transglutaminase IgA (tTGA) antibodies and IgA concentrations were measured in 73 patients with migraine (age range 6-17 years) and the control group (n = 147). Patients having positive tTGA antibodies underwent duodenal biopsy. Four patients (5.5%) from the study group and one (0.6%) from the control group had positive tTGA antibody titres (P < 0.05). Three patients with migraine had normal duodenal histology and were considered as potential CD. One patient from the study group and one from the control group declined to have biopsy. tTGA antibody is considered as a reliable indicator for the presence of CD. However, some patients with positive antibodies may have normal biopsy initially and are classified as having potential CD. Our finding of a higher prevalance of tTGA antibodies in paediatric migraine patients suggests that an association between migraine and CD might exist.
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