CC BY 4.0 · Journal of Child Science 2021; 11(01): e60-e64
DOI: 10.1055/s-0041-1724033
Original Article

Investigation of Tissue Transglutaminase Antibody Normalization in Response to Gluten-Free Diet in Children with Celiac Disease

Mohsen Pour Ebrahimi
1   Pediatric Gastroenterology and Hepatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
,
Hosein Alimadadi
1   Pediatric Gastroenterology and Hepatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
,
Mehri Najafi
1   Pediatric Gastroenterology and Hepatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
,
Mohammad Vasei
2   Cell Therapies Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Shariati Hospital, Tehran, Iran
,
1   Pediatric Gastroenterology and Hepatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
› Author Affiliations
Funding None.

Abstract

A very limited amount of data are available regarding the follow-up of celiac disease (CD) treatment in Iran. The aim of this study is to investigate antitissue transglutaminase (atTG) normalization interval and the associated factors in CD patients. This retrospective study included CD patients enrolled in Children's Medical Center, Tehran University of Medical Sciences. The initial atTG titer and histological evaluation (with Marsh grade ≥2) were recorded. The atTG titer was assessed in each follow-up until the time of normalization where children were strictly on gluten-free diet. The age at the time of diagnosis, gender, Marsh grade at the time of diagnosis, other comorbidities, and family history of CD patients were recorded to determine the association of these factors with antibody normalization interval. In total, 71 patients were recruited in the study of which 34 (47.89%) subjects had atTG level below 20 U/mL at the average interval of 31.36 ( ±  2.89) months (95% confidence interval: 25.7–37.02). There was no significant difference between the antibody normalization interval and different age ranges and Marsh grade. Cox regression demonstrated that gender, age ranges, Marsh grade, positive family history of CD, and the presence of comorbidities did not significantly predict longer antibody normalization interval.

Note

All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.


Authors' Contributions

M.P.E. and H.A. conceptualized and designed the study, drafted the initial manuscript, and reviewed and revised the manuscript. P.R. designed the data collection instruments, collected data, performed the initial analyses, and reviewed and revised the manuscript. M.N. and M.V. coordinated and supervised data collection, and critically reviewed the manuscript for important intellectual content.




Publication History

Received: 21 October 2020

Accepted: 25 December 2020

Article published online:
03 March 2021

© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
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  • References

  • 1 Vriezinga SL, Schweizer JJ, Koning F, Mearin ML. Coeliac disease and gluten-related disorders in childhood. Nat Rev Gastroenterol Hepatol 2015; 12 (09) 527-536
  • 2 Lundin KE, Qiao S-W, Snir O, Sollid LM. Coeliac disease - from genetic and immunological studies to clinical applications. Scand J Gastroenterol 2015; 50 (06) 708-717
  • 3 Celiac U. Professional eXG, newsletters/january-2011-professional-exg. Accessed 2018 at: https://ijcp.in/Admin/CMS/PDF/14.%20Pediatrics_IJCP_March_2018.pdf
  • 4 Hoffenberg EJ, MacKenzie T, Barriga KJ. et al. A prospective study of the incidence of childhood celiac disease. J Pediatr 2003; 143 (03) 308-314
  • 5 Fasano A. Clinical presentation of celiac disease in the pediatric population. Gastroenterology 2005; 128 (04) (Suppl. 01) S68-S73
  • 6 Walker-Smith. Revised criteria for diagnosis of celiac disease. J Arch Dis Child 1990; 65: 909-911
  • 7 Lähdeaho M-L, Mäki M, Laurila K, Huhtala H, Kaukinen K. Small- bowel mucosal changes and antibody responses after low- and moderate-dose gluten challenge in celiac disease. BMC Gastroenterol 2011; 11 (01) 129
  • 8 Husby S, Murray JA, Katzka DA. AGA clinical practice update on diagnosis and monitoring of celiac disease-changing utility of serology and histologic measures: expert review. Gastroenterology 2019; 156 (04) 885-889
  • 9 Stuckey C, Lowdon J, Howdle P. Joint BAPEN and British Society of Gastroenterology Symposium on ‘Coeliac disease: basics and controversies’. Dietitians are better than clinicians in following up coeliac disease. Proc Nutr Soc 2009; 68 (03) 249-251
  • 10 Biagi F, Andrealli A, Bianchi PI, Marchese A, Klersy C, Corazza GR. A gluten-free diet score to evaluate dietary compliance in patients with coeliac disease. Br J Nutr 2009; 102 (06) 882-887
  • 11 Husby S, Koletzko S, Korponay-Szabó IR. et al; ESPGHAN Working Group on Coeliac Disease Diagnosis, ESPGHAN Gastroenterology Committee, European Society for Pediatric Gastroenterology, Hepatology, and Nutrition. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 2012; 54 (01) 136-160
  • 12 Rubio-Tapia A, Hill ID, Kelly CP, Calderwood AH, Murray JA. American College of Gastroenterology. ACG clinical guidelines: diagnosis and management of celiac disease. Am J Gastroenterol 2013; 108 (05) 656-676 , quiz 677
  • 13 Fang H, King KS, Larson JJ. et al. Undetectable negative tissue transglutaminase IgA antibodies predict mucosal healing in treated coeliac disease patients. Aliment Pharmacol Ther 2017; 46 (07) 681-687
  • 14 Hopper AD, Hadjivassiliou M, Hurlstone DP. et al. What is the role of serologic testing in celiac disease? A prospective, biopsy-confirmed study with economic analysis. Clin Gastroenterol Hepatol 2008; 6 (03) 314-320
  • 15 Hussain S, Sabir MU, Afzal M, Asghar I. Coeliac disease--clinical presentation and diagnosis by anti tissue transglutaminase antibodies titre in children. J Pak Med Assoc 2014; 64 (04) 437-441
  • 16 Vécsei AK, Graf UB, Vogelsang H. Follow-up of adult celiac patients: which noninvasive test reflects mucosal status most reliably?1. Endoscopy 2009; 41 (02) 123-128
  • 17 Gidrewicz D, Potter K, Trevenen CL, Lyon M, Butzner JD. Evaluation of the ESPGHAN Celiac Guidelines in a North American pediatric population. Am J Gastroenterol 2015; 110 (05) 760-767
  • 18 Marsh MN. Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity (‘celiac sprue’). Gastroenterology 1992; 102 (01) 330-354
  • 19 United European Gastroenterology.. When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001. Eur J Gastroenterol Hepatol 2001; 13 (09) 1123-1128
  • 20 Waisbourd-Zinman O, Hojsak I, Rosenbach Y. et al. Spontaneous normalization of anti-tissue transglutaminase antibody levels is common in children with type 1 diabetes mellitus. Dig Dis Sci 2012; 57 (05) 1314-1320
  • 21 Gidrewicz D, Trevenen CL, Lyon M, Butzner JD. Normalization time of celiac serology in children on a gluten-free diet. J Pediatr Gastroenterol Nutr 2017; 64 (03) 362-367
  • 22 Isaac DM, Rajani S, Yaskina M, Huynh HQ, Turner JM. Antitissue transglutaminase normalization postdiagnosis in children with celiac disease. J Pediatr Gastroenterol Nutr 2017; 65 (02) 195-199
  • 23 Sud S, Marcon M, Assor E, Palmert MR, Daneman D, Mahmud FH. Celiac disease and pediatric type 1 diabetes: diagnostic and treatment dilemmas. Int J Pediatr Endocrinol 2010; 2010 (01) 161285
  • 24 Hill ID, Dirks MH, Liptak GS. et al; North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr 2005; 40 (01) 1-19
  • 25 Liu E, Bao F, Barriga K. et al. Fluctuating transglutaminase autoantibodies are related to histologic features of celiac disease. Clin Gastroenterol Hepatol 2003; 1 (05) 356-362
  • 26 Hogen Esch CE, Wolters VM, Gerritsen SA. et al. Specific celiac disease antibodies in children on a gluten-free diet. Pediatrics 2011; 128 (03) 547-552
  • 27 Fabiani E, Catassi C. International Working Group. The serum IgA class anti-tissue transglutaminase antibodies in the diagnosis and follow up of coeliac disease. Results of an international multi-centre study. International Working Group on Eu-tTG. Eur J Gastroenterol Hepatol 2001; 13 (06) 659-665
  • 28 Ciacci C, Cavallaro R, della Valle N, d'Argenio G. The use of serum tTG-ab assay in patients on gluten-free diet as a measure of dietetic compliance. Gastroenterology 2002; 122 (02) 588