Circulating microRNAs as potential non-invasive biomarkers in pediatric patients with celiac disease

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorAmr K.S.
dc.contributor.authorBayoumi F.S.
dc.contributor.authorEissa E.
dc.contributor.authorAbu-Zekry M.
dc.contributor.otherMedical molecular genetics Department
dc.contributor.otherNational Research Centre
dc.contributor.otherCairo
dc.contributor.otherEgypt; Immunogenetics Department
dc.contributor.otherNational Research Centre
dc.contributor.otherCairo
dc.contributor.otherEgypt; Microbiology and Immunology Department
dc.contributor.otherMSA University
dc.contributor.otherEgypt; Immunogenetics Department
dc.contributor.otherNational Research Centre
dc.contributor.otherCairo
dc.contributor.otherEgypt; Abu El Reesh Children�s Hospital
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:40:43Z
dc.date.available2020-01-09T20:40:43Z
dc.date.issued2019
dc.descriptionScopus
dc.description.abstractCeliac disease is an enteropathy induced by ingestion of gluten triggering an immune response in genetically predisposed individuals. MiRNAs are small non-coding RNAs that have a role as regulators of gene expression at the post transcriptional level. The aim of this study is to evaluate the possibility of using circulating miRNAs as non-invasive biomarkers in pediatric patients with celiac disease. In addition, we examine the effect of a gluten-free diet on the expression of these miRNAs in serum of CD patients. The expression pattern of miR-21 and miR-31 was estimated in serum of 25 untreated CD patients (recently diagnosed), 25 treated CD patients (on gluten-free diet) and 20 healthy controls using qRT-PCR. Our results demonstrated the significant up-regulation of microRNA-21 in the untreated celiac patients in comparison with the treated group and healthy controls. Moreover, miR-31 expression was significantly under-expressed in the untreated celiac patients in comparison with the treated group and healthy controls. Furthermore, the results showed that miR-21 expression level was significantly positively correlated with the tTG IgA auto-antibodies. In conclusion, circulating miRNA-21 and miRNA-31 could serve as potential non-invasive biomarkers for pediatric CD patients. � 2019, EDRA S.p.A. All rights reserved.en_US
dc.identifier.doihttps://doi.org/10.23822/EurAnnACI.1764-1489.90
dc.identifier.doiPubMedID30983306
dc.identifier.issn17641489
dc.identifier.otherhttps://doi.org/10.23822/EurAnnACI.1764-1489.90
dc.identifier.otherPubMedID30983306
dc.identifier.urihttps://t.ly/YZZnJ
dc.language.isoEnglishen_US
dc.publisherElsevier B.V.
dc.publisherEDRA S.p.Aen_US
dc.relation.ispartofseriesEuropean Annals of Allergy and Clinical Immunology
dc.relation.ispartofseries51
dc.subjectOctober University for Modern Sciences and Arts
dc.subjectجامعة أكتوبر للعلوم الحديثة والآداب
dc.subjectUniversity of Modern Sciences and Arts
dc.subjectMSA University
dc.subjectAutoantibodiesen_US
dc.subjectBiomarkersen_US
dc.subjectCeliac diseaseen_US
dc.subjectGluten free dieten_US
dc.subjectMicroRNAen_US
dc.subjectimmunoglobulin A antibodyen_US
dc.subjectmicroRNA 21en_US
dc.subjectmicroRNA 31en_US
dc.subjectprotein glutamine gamma glutamyltransferaseen_US
dc.subjectadolescenten_US
dc.subjectArticleen_US
dc.subjectceliac diseaseen_US
dc.subjectchilden_US
dc.subjectchildhood diseaseen_US
dc.subjectclinical articleen_US
dc.subjectcontrolled studyen_US
dc.subjectdown regulationen_US
dc.subjectfemaleen_US
dc.subjectgene expressionen_US
dc.subjectgluten free dieten_US
dc.subjecthumanen_US
dc.subjectmaleen_US
dc.subjectreverse transcription polymerase chain reactionen_US
dc.subjectupregulationen_US
dc.titleCirculating microRNAs as potential non-invasive biomarkers in pediatric patients with celiac diseaseen_US
dc.typeArticleen_US
dcterms.isReferencedByKenrick, K., Day, A.S., Coeliac disease: Where are we in 2014? (2014) Aust Fam Physician, 43 (10), pp. 674-678; Buoli Comani, G., Panceri, R., Dinelli, M., MiRNA-regulated gene expression differs in celiac disease patients according to the age of presentation (2015) Genes Nutr, 10 (5), p. 482; Lebwohl, B., Sanders, D.S., Green, P.H.R., Coeliac disease (2018) Lancet, 391 (10115), pp. 70-81; Felli, C., Baldassarre, A., Masotti, A., Intestinal and Circulating MicroRNAs in Coeliac Disease (2017) Int J Mol Sci, 18 (9). , pii; Magni, S., Buoli Comani, G., Elli, L., MiRNAs affect the expression of innate and adaptive immunity proteins in celiac disease (2014) Am J Gastroenterol, 109 (10), pp. 1662-1674; Vaira, V., Roncoroni, L., Barisani, D., MicroRNA profiles in coeliac patients distinguish different clinical phenotypes and are modulated by gliadin peptides in primary duodenal fibroblasts (2014) Clin Sci (Lond), 126 (6), pp. 417-423; Elli, L., Bergamini, C.M., Bardella, M.T., Transglutaminases in inflammation and fibrosis of the gastrointestinal tract and the liver (2009) Dig Liver Dis, 41 (8), pp. 541-550; Bascu��n-Gamboa, K.A., Araya-Quezada, M., P�rez-Bravo, F., MicroRNAs: An epigenetic tool to study celiac disease (2014) Rev Esp En-Ferm Dig, 106 (5), pp. 325-333; Zhang, L., Cheng, J., Fan, X.M., MicroRNAs: New therapeutic targets for intestinal barrier dysfunction (2014) World J Gastroenterol, 20 (19), pp. 5818-5825; Esteller, M., Non-coding RNAs in human disease (2011) Nat Rev Genet, 12 (12), pp. 861-874; Guo, H., Ingolia, N.T., Weissman, J.S., Mammalian micro-RNAs predominantly act to decrease target mRNA levels (2010) Nature, 466 (7308), pp. 835-840; Dai, R., Ahmed, S.A., MicroRNA, a new paradigm for understanding immunoregulation, inflammation, and autoimmune diseases (2011) Transl Res, 157 (4), pp. 163-179; Capuano, M., Iaffaldano, L., Tinto, N., MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients (2011) Plos One, 6 (12); Husby, S., Koletzko, S., Korponay-Szab�, I.R., 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 (2012) J Pediatr Gastroenterol Nutr, 54 (1), pp. 136-160; Peck, B.C., Weiser, M., Lee, S.E., MicroRNAs Classify Different Disease Behavior Phenotypes of Crohn�s Disease and May Have Prognostic Utility (2015) Inflamm Bowel Dis, 21 (9), pp. 2178-2187; Ludwig, K., Fassan, M., Mescoli, C., PDCD4/miR-21 dysreg-ulation in inflammatory bowel disease-associated carcinogenesis (2013) Virchows Arch, 462 (1), pp. 57-63; Wu, F., Zhang, S., Dassopoulos, T., Identification of microRNAs associated with ileal and colonic Crohn�s disease (2010) Inflamm Bowel Dis, 16 (10), pp. 1729-1738; Silva, M.A., L�pez, C.B., Riverin, F., Characterization and distribution of colonic dendritic cells in Crohn�s disease (2004) Inflamm Bowel Dis, 10 (5), pp. 504-512; Cekaite, L., Clancy, T., Sioud, M., Increased miR-21 expression during human monocyte differentiation into DCs (2010) Front Biosci (Elite Ed), 2 (3), pp. 818-828; Paraskevi, A., Theodoropoulos, G., Papaconstantinou, I., Circulating MicroRNA in inflammatory bowel disease (2012) J Crohns Colitis, 6 (9), pp. 900-904; Yang, Y., Ma, Y., Shi, C., Overexpression of miR-21 in patients with ulcerative colitis impairs intestinal epithelial barrier function through targeting the Rho GTPase RhoB (2013) Biochem Biophys Res Commun, 434 (4), pp. 746-752; Shi, C., Liang, Y., Yang, J., MicroRNA-21 knockout improve the survival rate in DSS induced fatal colitis through protecting against inflammation and tissue injury (2013) Plos One, 8 (6); Olaru, A.V., Selaru, F.M., Mori, Y., Dynamic changes in the expression of microRNA-31 during inflammatory bowel disease-associated neoplastic transformation (2011) Inflamm Bowel Dis, 17 (1), pp. 221-231; B�res, N.J., Kiss, Z., Sztupinszki, Z., Altered mucosal expression of microRNAs in pediatric patients with inflammatory bowel disease (2017) Dig Liver Dis, 49 (4), pp. 378-387; Amr, K.S., Bayoumi, F.S., Elgengehy, F.T., The role of microR-NA-31 and microRNA-21 as regulatory biomarkers in the activation of T lymphocytes of Egyptian lupus patients (2016) Rheumatol Int, 36 (11), pp. 1617-1625
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