Prevalence of Tissue Transglutamase Antibodies in cases of Celiac Disease
Keywords:
Celiac disease, anti-tissue transglutaminase, anti- glidin, gastroenteritisAbstract
Celiac disease is a human leukocyte antigen-DQ2 (or DQ8) associated autoimmune disorder of the small intestine induced by dietary exposure to wheat gliadin, barley hordein, rye secalin and possibly oat avenis.
It is characterized by mucosal damage, loss of absorptive villi and hyperplasia of the crypts leading to malabsorption. In addition, to nutrient deficiencies and growth failure, prolonged untreated celiac disease is associated with an increased risk of malignancy, especially intestinal T cell lymphoma. Tissue transglutaminase antibody tTG antibodies of isotype IgA and IgG is a simple, sensitive and specific noninvasive screening test for diagnosis of celiac disease, particularly in developing countries like Pakistan. In current study from September 2010 to May 2014, samples from 3643 cases referred to Dow Diagnostic Research and Reference
lab were screened for serum IgA and IgG for tissue transglutaminase by ELISA. Results showed that about 1290 patients were anti TtG IgA positive including male and female with a ratio of 1:1.4 respectively, indicating an active stage of the disease. Children (age group between 0 to 16) showed a greater prevalence i.e 37% as compared to other age group. However IgG against tissue transglutaminase didn’t show any significant prevalence pattern.
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Ludvigsson J, Leffler D, Bai JC, et al. 2012 The Oslodefinitions for coeliac disease-related terms. Gut Feb 16.
Stern M, Ciclitira P, Van Eckert R, et al. 2001 Analysis and clinical effects of gluten in coeliac disease. Eur J GastroenterolHepatol; 13: 741–7.
Sapone A, Bai JC, Ciacci C, et al. Spectrum of gluten-related disorders: consensus on new nomenclature and classification. BMC Med 2012, 10: 13.
Marsh MN. 1992 Gluten major histocompatibility complex, and the small intestine. Gastroenterology; 102: 330–54.
Catassi C, Rätsch IM, Gandolfi L, et al. 1999 Why iscoeliac disease endemic in the people of Sahara? Lancet; 354: 647–8.
Lionetti E, Catasssi C. New clues in celiac disease epidemiology, pathogenesis, clinical manifestations, and treatment. Int Rev Immunol 2011; 30: 219–31.
Sood A, Midha V, Sood N, et al. 2006 Prevalence of CD among school children in Punjab, North India. J Gastroenterol Hepatol; 21: 1622–5.
Aziz S, Muzaffar R, Zafar MN, et al. 2007 Celiac disease in children with persistent diarrhea and failure to thrive. J Coll Physicians Surg Pak;17: 554–7.
Roston A, Dubé C, Cranney A, et al. 2007 The diagnostic accuracy of serologic test for celiac disease: a systematic review. Gastroenterology 2005; 128: S38–S46.
Leffler D, Scuppan D. 2010 Update on serologic testing in celiac disease. Am J Gastroenterol; 105: 2520–4.
Kurppa K, Collin P, Mäki M, et al. 2011 Celiac disease and health-related quality of life. Expert Rev GastroenterolHepatol; 5: 83–90.
Nachman F, del Campo MP, González A, et al. 2010 Long-term deterioration of quality of life in adult patients with celiac disease is associated with treatment noncompliance. Dig Liver Dis; 42: 685–91.
Cranney A, Rostom A, Sy R, et al. 2005 Consequences of testing for celiac disease. Gastroenterology; 128: S109–S120.
Brousse N, Meijer JW. 2005 Malignant complications of coeliac disease. Best Pract Res ClinGastroenterol; 19: 401–12.
Ludvigsson JF, Montgomery SM, Ekbom A, et al. 2009 Small-intestinal histopathology and mortality risk in celiac disease. JAMA; 302: 1171–8.
Gomez JC, Selvaggio GS, Viola M, et al. Prevalence of celiac disease in Argentina: screening of an adult population in the La Plata area. Am J Gastroenterol 2001; 96: 2004.
Catassi C, Kryzak D, Bhatti B, et al 2010. Natural history of celiac disease autoimmunity in a USA cohort followed since 1974. Ann Med; 42: 530–8
Maki M, Mustalhati K, Kokkonen J, et al. 2003 Prevalence of celiac disease among children in Finland. N Engl J Med; 348: 2517–24.
Sollid LM, Thorsby E. 1993 HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis. Gastroenterology; 105: 910–22.
Abadie V, Sollid L, Barreiro LB, et al. Integration of genetic and immunological insights into a modelof celiac disease pathogenesis. Annu Rev Immunol 2011; 29: 493–525.
Gandolfi L, Pratesi R, Cordoba JC, et al 2000. Prevalence of CD among blood donors in Brazil. Am J Gastroenterol; 95: 689–92.
Green PH, Jabri B. 2003 Coeliac disease. Lancet; 362: 383–91.
Ciclitira PJ. 2001 Celiac disease: a technical review. Gastroenterology; 120: 1526–40.
Green PH, Cellier C. 2007 Celiac disease. N Engl J Med; 357: 1731–43.
Pulido OM, Gillespie Z, Zarkadas M, et al. 2009Introduction of oats in the diet of individuals with celiac disease: a systematic review. Adv Food Nutr Res; 57: 235–85.
Collin P. 2005 Should adults be screened for celiac disease? What are the benefits and harm of screening? Gastroenterology 128: S104–S108.
Hoffenberg EJ. Should all children be screened for celiac disease? Gastroenterology 2005; 128: S98–S103.
Sugai E, Nachman F, Váquez H, et al. 2010 Dynamics of celiac disease–specific serology after initiation of a
gluten-free diet and use in the assessment of compliance with treatment. Dig Liver Dis; 42: 352–8.
Akobeng AK, Thomas AG. 2008 Systematic review: tolerable amount of gluten for people with coeliac disease. Aliment PharmacolTher; 27:1044–52.
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