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Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries
AIM: To verify the precision and accuracy of transglutaminase antibodies (TGA) assays across Mediterranean countries. METHODS: This study involved 8 referral centres for celiac disease (CD) in 7 Mediterranean countries. A central laboratory prepared 8 kits of 7 blinded and randomized serum samples,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487508/ https://www.ncbi.nlm.nih.gov/pubmed/28706427 http://dx.doi.org/10.3748/wjg.v23.i24.4437 |
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author | Smarrazzo, Andrea Magazzù, Giuseppe Ben-Hariz, Mongi Legarda Tamara, Maria Velmishi, Virtut Roma, Elefhteria Kansu, Aydan Mičetić-Turk, Dušanka Bravi, Enzo Stellato, Pio Arcidiaco, Carmela Greco, Luigi |
author_facet | Smarrazzo, Andrea Magazzù, Giuseppe Ben-Hariz, Mongi Legarda Tamara, Maria Velmishi, Virtut Roma, Elefhteria Kansu, Aydan Mičetić-Turk, Dušanka Bravi, Enzo Stellato, Pio Arcidiaco, Carmela Greco, Luigi |
author_sort | Smarrazzo, Andrea |
collection | PubMed |
description | AIM: To verify the precision and accuracy of transglutaminase antibodies (TGA) assays across Mediterranean countries. METHODS: This study involved 8 referral centres for celiac disease (CD) in 7 Mediterranean countries. A central laboratory prepared 8 kits of 7 blinded and randomized serum samples, with a titrated amount of Human TGA IgA. Each sample was analysed three times on three different days, with each centre running a total of 21 tests. The results were included in a blindly coded report form, which was sent to the coordinator centre. The coordinator estimated the mean coefficient of Variation (CoVar = σ/μ), the mean accuracy (Accur = Vobserved - Vreal) and the mean percent variation (Var% = [(Vobserved - Vreal)/Vreal] × 100). RESULTS: The analysis showed that 79.17% of the mean variation fell between -25% and +25% of the expected value, with the accuracy and precision progressively increasing with higher titres of TGA. From values 1.25 times greater than the normal cut-off, the measurements were highly reliable. CONCLUSION: TGA estimation is a crucial step for the diagnosis of CD; given its accuracy and precision, clinicians could be confident in establishing a diagnosis. |
format | Online Article Text |
id | pubmed-5487508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-54875082017-07-13 Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries Smarrazzo, Andrea Magazzù, Giuseppe Ben-Hariz, Mongi Legarda Tamara, Maria Velmishi, Virtut Roma, Elefhteria Kansu, Aydan Mičetić-Turk, Dušanka Bravi, Enzo Stellato, Pio Arcidiaco, Carmela Greco, Luigi World J Gastroenterol Observational Study AIM: To verify the precision and accuracy of transglutaminase antibodies (TGA) assays across Mediterranean countries. METHODS: This study involved 8 referral centres for celiac disease (CD) in 7 Mediterranean countries. A central laboratory prepared 8 kits of 7 blinded and randomized serum samples, with a titrated amount of Human TGA IgA. Each sample was analysed three times on three different days, with each centre running a total of 21 tests. The results were included in a blindly coded report form, which was sent to the coordinator centre. The coordinator estimated the mean coefficient of Variation (CoVar = σ/μ), the mean accuracy (Accur = Vobserved - Vreal) and the mean percent variation (Var% = [(Vobserved - Vreal)/Vreal] × 100). RESULTS: The analysis showed that 79.17% of the mean variation fell between -25% and +25% of the expected value, with the accuracy and precision progressively increasing with higher titres of TGA. From values 1.25 times greater than the normal cut-off, the measurements were highly reliable. CONCLUSION: TGA estimation is a crucial step for the diagnosis of CD; given its accuracy and precision, clinicians could be confident in establishing a diagnosis. Baishideng Publishing Group Inc 2017-06-28 2017-06-28 /pmc/articles/PMC5487508/ /pubmed/28706427 http://dx.doi.org/10.3748/wjg.v23.i24.4437 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Observational Study Smarrazzo, Andrea Magazzù, Giuseppe Ben-Hariz, Mongi Legarda Tamara, Maria Velmishi, Virtut Roma, Elefhteria Kansu, Aydan Mičetić-Turk, Dušanka Bravi, Enzo Stellato, Pio Arcidiaco, Carmela Greco, Luigi Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title | Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title_full | Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title_fullStr | Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title_full_unstemmed | Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title_short | Variability of anti-human transglutaminase testing in celiac disease across Mediterranean countries |
title_sort | variability of anti-human transglutaminase testing in celiac disease across mediterranean countries |
topic | Observational Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487508/ https://www.ncbi.nlm.nih.gov/pubmed/28706427 http://dx.doi.org/10.3748/wjg.v23.i24.4437 |
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