Phenotype and Natural History of Children With Coexistent Inflammatory Bowel Disease and Celiac Disease

Author:

Bramuzzo Matteo1ORCID,Lionetti Paolo2,Miele Erasmo3,Romano Claudio4,Arrigo Serena56,Cardile Sabrina7,Di Nardo Giovanni8ORCID,Illiceto Maria Teresa9,Pastore Maria10,Felici Enrico11,Fuoti Maurizio12,Banzato Claudia13,Citrano Michele14,Congia Mauro15,Norsa Lorenzo16ORCID,Pozzi Elena17,Zuin Giovanna18,Agrusti Anna19,Bianconi Martina20,Grieco Claudia3,Giudici Fabiola2122ORCID,Aloi Marina23,Alvisi Patrizia24

Affiliation:

1. Gastroenterology, Digestive Endoscopy and Nutrition Unit, Institute for Maternal and Child Health, IRCCS “Burlo Garofolo,” Trieste, Italy

2. Department NEUROFARBA, University of Florence, Meyer Children’s Hospital, Florence, Italy

3. Department of Translational Medical Sciences, Section of Pediatrics, University of Naples “Federico II,” Naples, Italy

4. Unit of Pediatric Gastroenterology and Cystic Fibrosis, Department of Human Pathology in Adulthood and Childhood “G. Barresi,” University of Messina, Messina, Italy

5. Pediatric Gastroenterology and Endoscopy Unit, Institute “Giannina Gaslini,” Genoa, Italy

6. Department of Pediatrics, “F. Del Ponte” Hospital, University of Insubria, Varese, Italy

7. Department of Hepatology, Gastroenterology and Nutrition, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy

8. NESMOS Department, Faculty of Medicine and Psychology, Sapienza University of Rome, Sant’Andrea University Hospital, Rome, Italy

9. Pediatric Gastroenterology and Endoscopic Unit, Department of Pediatrics, “Santo Spirito” Hospital, Pescara, Italy

10. Pediatric Department, “Casa Sollievo della Sofferenza” Hospital, IRCCS, San Giovanni Rotondo, Italy

11. Pediatric and Pediatric Emergency Unit, “Umberto Bosio” Center for Digestive Diseases, The Children Hospital, AO SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy

12. Pediatric Gastroenterology and Endoscopy Unit Children’s Hospital, ASST Spedali Civili, Brescia, Italy

13. Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, Pediatric Division, University of Verona, Verona, Italy

14. Department of Pediatrics, “Ospedali Riuniti Villa Santa Sofia-Cervello,” Palermo, Italy

15. Pediatric Clinic and Rare Diseases, Microcitemic Pediatric Hospital Antonio Cao, Azienda Ospedaliera Brotzu, Cagliari, Italy

16. Pediatric Hepatology Gastroenterology and Transplantation, Papa Giovanni XXIII Hospital, Bergamo, Italy

17. Department of Pediatrics, Vittore Buzzi Children’s Hospital, University of Milan, Milan, Italy

18. Pediatric Department, University of Milano Bicocca, FMBBM, San Gerardo Hospital, Monza, Italy

19. Department of Medicine, Surgery, and Health Sciences, University of Trieste, Trieste, Italy

20. Department of Health Sciences, University of Florence, Meyer children’s Hospital, Florence, Italy

21. Biostatistics Unit, Department of Medicine, Surgery and Health Sciences, Cattinara Hospital, University of Trieste, Trieste, Italy

22. Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Padua, Italy

23. Women’s and Children’s Health Department, Pediatric Gastroenterology and Hepatology Unit, Sapienza University of Rome, Rome, Italy

24. Pediatric Gastroenterology Unit, Maggiore Hospital, Bologna, Italy

Abstract

Abstract Background Adult patients with both inflammatory bowel disease (IBD) and celiac disease (CeD) have peculiar phenotypic features. This study aimed at describing the characteristics and natural history of children with both IBD and CeD. Methods This was a case-control study based on a national registry. Cases included children diagnosed with both IBD and CeD. Two matched IBD controls without CeD, and 2 matched CeD controls were selected for each case. Inflammatory bowel disease phenotype and natural history, comprising growth and pubertal development, were compared between groups. Results Forty-nine (1.75%) patients with IBD and CeD were identified out of 2800 patients with IBD. Compared with patients with IBD alone, patients with IBD and CeD presented more frequently with autoimmune diseases (odds ratio, 2.81; 95% CI, 0.97–8.37; P = 0.04). Ileocolonic localization (46.1% vs 73.1%), treatment with azathioprine (46.2% vs 71.2%), and anti-TNF biologics (46.2% vs 69.2%) were less common in patients with Crohn’s disease and CeD than in patients with Crohn’s disease alone. Patients with ulcerative colitis and CeD had an increased risk of colectomy despite similar medical treatments compared with patients with ulcerative colitis alone (13.0% vs 0%). Pubertal delay was more common in patients with IBD and CeD compared with patients with IBD alone (14.9% vs 3.2%; odds artio, 5.24; 95% CI, 1.13–33.0; P = 0.02) and CeD alone (14.9% vs 1.1%; P = 0.002). Conclusions Children with IBD and CeD may have peculiar features with a higher risk for autoimmune diseases, colectomy, and pubertal delay compared with IBD alone.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

Reference40 articles.

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