Prevalen of ceceliac disease in patients of Hospital UNIVALLE 2016- 2017
DOI:
https://doi.org/10.52428/20756208.v13i34.488Keywords:
Celiac disease, Autoinmunity, Serological tests, Enteropathy, GlutenAbstract
Celiac disease is a chronic enteropathy of the small intestinal mucosa caused by gluten intolerance, which results in villous atrophy, malabsorption and clinical symptoms that manifest in childhood or adulthood. The pathogenesis consists in the interaction of the proteins present in wheat, barley, oats and rye between genetic, immunological and environmental factors, which interact with the molecules of human leukocyte antigens to activate an immunological response in the mucosa of the small intestine, producing tissue damage.
Serological tests and duodenal biopsy (the gold standard) are important for diagnosis. A retro-spective cross-sectional study was carried out on 23 patients who attended the specialty of gastroenterology at Hospital UNIVALLE Cochabamba between 2016 -2017, the tests EMA, tTGA and antigliadin and upper endoscopy were determined, observing greater positivity in the female sex than in the male.
Studies conducted in Europe, the United States and Latin America have found frequencies of this disease between 1/100 - 1/300 and the diagnosis depends on the degree of clinical suspicion. The prevalence data found confirm that celiac disease constitutes a public health problem in our country, which could justify the establishment of a study program. The regions with the highest prevalence (1 %) are Europe and the USA, where traditional food is based on foods with gluten. 10801 patients were attended during the 2016 and 2017 procedures, with a prevalence of 0,21 %, with a low prevalence in our country, due to the lack of studies and the clinic.
Downloads
References
FASANO A, BERTI l, GERARDUZZI T, NOT T, COLLETTI R, DRAGO S, et al. Prevalence of Celiac Disease in At-Risk and Not- At-Risk Groups in the United States. EE.UU.: Arch Intern Med 2003. pg. 286-292. DOI: https://doi.org/10.1001/archinte.163.3.286
HORWITZ A, SKAABY T, KARHUS LL, SCHWARZ P, JORGENSEN T, RUMESSEN JJ, et al. Screening for celiac disease in Danish adults. Chile: Scand J Gastroenterol 2015. DOI: https://doi.org/10.3109/00365521.2015.1010571
BURGER JP, ROOVERS EA, DRENTH JP, MEIJER JWyWAHAB PJ. Rising inci-dence of celiac disease in the Netherlands: an analysis of temporal trends from 1995 to 2010. EE.UU.: Scand J Gastroenterol 2014; 49 (8): 933-941. DOI: https://doi.org/10.3109/00365521.2014.915054
MINISTERIO DE SALUD DE CHILE. Encuesta Nacional de salud 2009-2010. Tomo l. [Internet] 2016 [Consultado en noviembre de 2017] Disponible en: www.minsal.cl/portal/url/item/bcb03d7bc28b64dfe040010165012d23.pdf
PETERS U, ASKLING J, GRIDLEY G, EKBOM A y LINET M. Causes of death in patients with celiac disease in a population-based Swedish Cohort. EE.UU.: Arch Intern Med 2003; 163:1566-1572. DOI: https://doi.org/10.1001/archinte.163.13.1566
CORRAO G, CORAZZA GR, BAGNARDI V, BRUSCO G, CIACCI C, COTTONE M, et al. Mortality in pa-tients with coeliac disease and their relatives: a cohort study. EE.UU.: Lancet 2001; 358: 356-361. DOI: https://doi.org/10.1016/S0140-6736(01)05554-4
KAGNOFF, M. Overview and Pathogenesis of Celiac Disease, California, EE.UU.: Gastroenterology 2005; 128:10-18. DOI: https://doi.org/10.1053/j.gastro.2005.02.008
KILMARTIN C, LYNCH S, ABUZAKOUK M, WIESER H y FEIGHERY C. Avenin fails to induce a Thl response in coeliac tissue following in vitro culture. Sevilla, España: Gut 2003; 52:47-52. DOI: https://doi.org/10.1136/gut.52.1.47
SHAN L, MOLBERG a, PARROT I, HAUSCH F, FILIZ F, GRAY G, et al. Structural basis for gluten intolerance in celiac sprue. Zurich, Suiza: Science 2002; 297:2275-2279. DOI: https://doi.org/10.1126/science.1074129
Dl SABATINO A y CORAZZA G. Coeliac disease. EE.UU.: Lancet 2009; 373:1480-1494. DOI: https://doi.org/10.1016/S0140-6736(09)60254-3
GREEN P y CELLIER C. Celiac disease. EE. UU.: N Engl J Med V. 2007; 357:1731-1743. DOI: https://doi.org/10.1056/NEJMra071600
MOHAMED B, FEIGHERY C, KELLY J, COATES C, O'SHEA U, BARNES L, et al. Increased Protein Expression of Matrix Metalloproteinases -1, -3, and -9 and TIMP-I in Patients with Gluten-Sensitive Enteropathy. EE.UU.: Dig Dis Sci. 2006; 51:1862-1868. DOI: https://doi.org/10.1007/s10620-005-9038-4
SOLLID LM y LIE BA. Celiac disease genetics: current concepts and practical applications. EE.UU.: Clin Gastroenterol Hepatol 2005; 3: pg. 843-851. Oslo, Norway. DOI: https://doi.org/10.1016/S1542-3565(05)00532-X
ARAYA M, OYARZÜN A, LUCERO Y, ESPINOSA N y PÉREZ-BRAVO F. DQ2, DQ7 and DQ8 Distribution and Clinical Manifestations in Celiac Cases and Their First-Degree Relatives. Chile: Nutrients 2015; 7:4955-4965. DOI: https://doi.org/10.3390/nu7064955
IVARSSON A, HERNELL O, STENLUND H y PERSSON LA. Breast-feeding protects against celiac disease. EE.UU.: Am J Clin Nutr 2002; 75:914-921. DOI: https://doi.org/10.1093/ajcn/75.5.914
LEBWOHL B, BLASER MJ, LUDVIQSSON JF, GREEN PH, RUNDLE A, SONNEN-BERG A, et al. Decreased risk of celiac disese in patients with Helicobacter pylori colonization. EE.UU.: Am J Epidemiol 2013; 178:1721-1730. DOI: https://doi.org/10.1093/aje/kwt234
O'LEARY C, WIC-NE-KE P, BUCKLEY S, OREGAN P, CRONIN CC, QUIGLEY E, et al. Celiac disease and irritable bowel-type symptoms. Reino Unido: Am J Gastroenterol 2002; 97:1463-1467. DOI: https://doi.org/10.1111/j.1572-0241.2002.05690.x
TRONCONE R, GRECO L, MAYER M, PAPARO F, CAPUTO N, MICILLO M, et al. Latent and potential coeliac disease. Säo Paulo, Brazil: Acta Paediatr 1996; 412:10-14. DOI: https://doi.org/10.1111/j.1651-2227.1996.tb14240.x
LUDVIGSSON J, LEFFLER D, BAI C, BIAGI F, FASANO A, GREEN P, et al. The Oslo definitions for coeliac disease and related terms. EE.UU.: Gut 2013; 62:43-52. DOI: https://doi.org/10.1136/gutjnl-2011-301346
VOLTA U, CAIO G, STANGHELLINI V y DE GIORGIO R. The changing clinical profile of celiac disease: a 15-year experience (1998-2012) in an Italian referral center. Italia: BMC Gastroenterol 2014; 14:194-202. DOI: https://doi.org/10.1186/s12876-014-0194-x
BRAR P, KWON GY, EGBUNA Il, HOLLERAN S, RAMAKRISHNAN R, BHAGAT G, et al. Lack of correlation of degree of villous atrophy with severity of clinical presentation of coeliac disease. Netherlands: Dig Liver Dis 2007; 39:26-29. DOI: https://doi.org/10.1016/j.dld.2006.07.014
MURRAY JA, RUBIO-TAPIA A, VAN DYKE CT, BROGAN DC, KNIPSCHIELD MA, LAHR B, et al. Mucosal atrophy in celiac disease: extent of involvement, correlation with clinical presentation, and response to treatment. Serbia: Clin Gastroenterol Hepatol 2008; 6:186-193. DOI: https://doi.org/10.1016/j.cgh.2007.10.012
MATYSIAK-BUDNIK T, MALAMUT G, DE SERRE N, GROSDIDIER E, SEGUIER S, BROUSSE N, et al. Longterm follow-up of 61 coeliac patients diagnosed in childhood: evolution toward latency is possible on a normal diet. EE.UU.: Gut 2007; 56:1379-1386. DOI: https://doi.org/10.1136/gut.2006.100511
CZAJA-BULSA G. Non coeliac gluten sensitivity. EE.UU.: Clin Nutr 2015; 34 DOI: https://doi.org/10.1016/j.clnu.2014.08.012
NAVARRO E y ARAYA M. Sensibilidad no celiaca al gluten. Una patologia mås que responde al gluten. Santiago de Chile, Chile Rev Med Chile 2015; 143:619-626. DOI: https://doi.org/10.4067/S0034-98872015000500010
LEFFLER DA y SCHUPPAN D. Update on serologic testing in celiac disease. EE.UU.: Am J Gastroenterol 2010; 105:2520-2524. DOI: https://doi.org/10.1038/ajg.2010.276
RUBIO-TAPIA A, HILL l, KELLY C, CALDERWOOD A y MURRAY J. ACG Clinical Guidelines: Diagnosis and Management of Celiac Disease. EE.UU.: Am J Gastroenterol 2013; 108:656-676. DOI: https://doi.org/10.1038/ajg.2013.79
ROSTOM A, DUBÉ C, CRANNEY A, SALOOJEE N, sy R, GARRITTY C, et al. The Diagnostic Accuracy of Serologic Tests for Celiac Disease: A Systematic Review. EE.UU.: Gastroenterology 2005; 128:38-46. DOI: https://doi.org/10.1053/j.gastro.2005.02.028
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2018 Jacqueline Borda Zambrana , Edson Flores , Sarah Vasquez y Yhassyre Abularach
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License 4.0 that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.