Screening for celiac disease among children with overweight and obesity: toward exploring celiac iceberg

Author:

Calcaterra Valeria12,Regalbuto Corrado13,Manuelli Matteo4,Klersy Catherine5,Pelizzo Gloria26,Albertini Riccardo7,Vinci Federica13,Larizza Daniela13,Leonard Maureen M.89,Cena Hellas410

Affiliation:

1. Pediatric and Adolescent Unit, Department of Internal Medicine , University of Pavia , Pavia , Italy

2. Pediatric Surgery Unit, Children’s Hospital "Vittore Buzzi" , Milano , Italy

3. Pediatric Endocrinologic Unit, Department of Maternal and Children’s Health , Fondazione IRCCS Policlinico San Matteo , Pavia , Italy

4. Laboratory of Dietetics and Clinical Nutrition, Department of Public Health, Experimental and Forensic Medicine , University of Pavia , Pavia , Italy

5. Biometry & Clinical Epidemiology, Scientific Direction , Fondazione IRCCS Policlinico San Matteo , Pavia , Italy

6. Department of Biomedical and Clinical Science “L. Sacco” , University of Milano , Milano , Italy

7. Laboratory of Clinical Chemistry , Fondazione IRCCS Policlinico San Matteo, Pavia , Italy

8. Center for Celiac Research and Treatment, Mass General Hospital for Children , Boston , Massachusetts , USA

9. Division of Pediatric Gastroenterology and Nutrition, Mass General Hospital for Children, Harvard Medical School , Boston , MA , USA

10. Clinical Nutrition and Dietetics Service, Unit of Internal Medicine and Endocrinology , ICS Maugeri IRCCS , Pavia , Italy

Abstract

Abstract Objectives The coexistence of celiac disease (CD) and obesity/overweight is not unusual. 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.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

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