Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/49376
DC FieldValueLanguage
dc.contributor.authorBaviera, Luis Carlos Blesaen_US
dc.contributor.authorAliaga, Ester Donaten_US
dc.contributor.authorOrtigosa, Luisen_US
dc.contributor.authorLitwin, Néstoren_US
dc.contributor.authorPeña-Quintana, Luisen_US
dc.contributor.authorMéndez, Virginiaen_US
dc.contributor.authorGonzález, Ma Victoriaen_US
dc.contributor.authorLópez-Manzanares, Javier Manzanaresen_US
dc.contributor.authorMéndez, Enriqueen_US
dc.contributor.authorKoninckx, Carmen Ribesen_US
dc.date.accessioned2018-11-24T06:51:52Z-
dc.date.available2018-11-24T06:51:52Z-
dc.date.issued2007en_US
dc.identifier.issn0277-2116en_US
dc.identifier.urihttp://hdl.handle.net/10553/49376-
dc.description.abstractObjective: To assay the efficiency for celiac disease (CD) screening of 2 immunochromatographic visual stick assays based on human recombinant tissue transglutaminase (tTG). One was the antitissue transglutaminase antibodies (AtTGA) stick for IgA/G antibodies to tTG detection, the other was the AtTGA/antigliadin antibodies (AGA) stick for IgA antibodies for tTG and/or gliadins. Patients and methods: In a prospective multicenter study, 4 pediatric gastroenterology units from Spain and 2 from Latin America enrolled 72 control children with a normal small bowel mucosa and 113 untreated patients with CD with Marsh type 3 lesions. Results: Evaluation of results by the gastroenterologists and by 2 independent observers at the coordination center showed a remarkably low interobserver variability. For the AtTGA stick, sensitivity was 96.5% and specificity was 98.6%. The AtTGA/AGA stick displayed a sensitivity of 94.5% and a specificity of 98.6% for AtTGA and a sensitivity of 63.1% and a specificity of 95.2% for AGA. The highest efficiency and positive likelihood ratio was obtained for the AtTGA stick, higher than for IgA AtTGA by enzyme-linked immunosorbent assay. One additional advantage was that previous investigation of total serum IgA levels could be eluded. The IgA AtTGA/AGA stick, with an efficiency of 95.1%, compared with 89.2% when the combined results of the 2 enzyme-linked immunosorbent assays were considered, turned out to be an excellent diagnostic tool for infants with no IgA deficiency. Conclusion: These 2 assays are extremely efficient for CD screening, by combining a high diagnostic accuracy with the simplicity and rapidity of visual methods.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Pediatric Gastroenterology and Nutritionen_US
dc.sourceJournal of Pediatric Gastroenterology and Nutrition[ISSN 0277-2116],v. 45(5), p. 546-550 (Noviembre 2007)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320503 Gastroenterologíaen_US
dc.subject3206 Ciencias de la nutriciónen_US
dc.subject.otherCeliac diseaseen_US
dc.subject.otherImmunochromatographic visual methoden_US
dc.subject.otherScreeningen_US
dc.titleCeliac disease screening by immunochromatographic visual assays: Results of a multicenter studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1097/MPG.0b013e31814794b9en_US
dc.identifier.scopus37349101234-
dc.contributor.authorscopusid23092785700-
dc.contributor.authorscopusid12244561600-
dc.contributor.authorscopusid54946469200-
dc.contributor.authorscopusid6602248106-
dc.contributor.authorscopusid6603266503-
dc.contributor.authorscopusid57198090907-
dc.contributor.authorscopusid23093912700-
dc.contributor.authorscopusid6505633093-
dc.contributor.authorscopusid7102731729-
dc.contributor.authorscopusid6506441836-
dc.description.lastpage550en_US
dc.description.firstpage546en_US
dc.relation.volume45en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.date.coverdateNoviembre 2007en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,102-
dc.description.jcrqQ1-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Nutrición-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0001-6052-5894-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNamePeña Quintana, Luis-
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