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Screening for celiac disease among children with overweight and obesity: toward exploring celiac iceberg
Valeria Calcaterra1,2, Corrado Regalbuto1,3, Matteo Manuelli4
1Pediatric and Adolescent Unit, Department of Internal Medicine, University of Pavia, Pavia, Italy.
Insights
Celiac disease (CD) screening in overweight children found a 4% prevalence. CD diagnosis was linked to lower fruit/vegetable intake and more frequent headaches, suggesting screening for unexplained headaches in this population.
Area of Science:
- Pediatrics
- Gastroenterology
- Immunology
Background:
- Celiac disease (CD) and obesity/overweight can coexist in children.
- Screening for CD in pediatric overweight/obesity populations is warranted.
Purpose of the Study:
- To determine the prevalence and clinical presentation of celiac disease (CD) in children with excessive weight gain.
- To investigate potential risk factors and associated symptoms in pediatric CD patients.
Main Methods:
- Screened 200 children with overweight/obesity for CD using serological markers (IgA, tTG-IgA, EMA-IgA).
- Performed esophagogastroduodenoscopy (EGDS) and HLA DQ2/DQ8 genetic testing for confirmed cases.
- Collected data on medical history, lifestyle, and dietary habits.
Main Results:
- Celiac disease (CD) was diagnosed in 4% (8/200) of children, confirmed by EGDS and genetic testing.
- CD patients reported lower weekly fruit and vegetable consumption (p=0.04).
- Headache (p=0.04) and a family history of autoimmune diseases (p=0.01) were more frequent in CD patients.
Conclusions:
- Celiac disease (CD) should be considered in the evaluation of children with excessive weight gain.
- Familial autoimmune predisposition is a potential risk factor for pediatric CD.
- Screening for CD in children with unexplained headaches, particularly those with overweight/obesity, is recommended.
Abstract:
Background The coexistence of celiac disease (CD) and obesity/overweight is not unusual. Objective We investigate the prevalence and clinical presentation of CD, detected by screening, among children with excessive weight gain. Methods We enrolled 200 children referred for overweight/obesity to our outpatient clinic. Medical history during pregnancy and childhood and lifestyle variables were recorded. Patients were screened for CD with total immunoglobulin A (IgA), IgA anti-transglutaminase (tTG-IgA) and IgA anti-endomysial antibodies (EMA-IgA). In subjects with positive autoantibodies, esophagogastroduodenoscopy (EGDS) was performed and genetic testing for HLA DQ2 and/or DQ8 haplotypes was tested. Results CD positive antibodies (tTg-IgA and EMA-IgA) were detected in eight patients (4%); in all subjects CD diagnosis was confirmed by HLA-DQ2 and/or DQ8 compatibility and EGDS. No association between CD and medical history during pregnancy and childhood or lifestyle variables was noted; however, a dietary difference was identified with those testing positive for CD also reporting a lower weekly consumption of fruits and vegetables (p=0.04). Headache was reported more frequently in patients with than without CD (p=0.04). Familiar positivity for autoimmune diseases was revealed in CD patients (p=0.01). Conclusion CD should be considered in children with excessive weight gain. Familial predisposition to other autoimmune diseases may represent a risk factor for development of CD. Even though the relationship between headache and CD is not well defined, the patients with headache of unknown origin should be screened for CD.
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