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Diagnostic accuracy of anti-DGP (IgG) for celiac disease
BACKGROUND: Celiac disease (CD) is an autoimmune enteropathy that is caused by the intake of gluten-containing grains in genetically susceptible humans. The gliadin and glutenin parts of wheat gluten are the essential factors that cause intestinal damage. OBJECTIVES: We analyzed the performance of a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071923/ https://www.ncbi.nlm.nih.gov/pubmed/37025242 http://dx.doi.org/10.4103/jfmpc.jfmpc_326_22 |
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author | Jafari, Seyed A. Alami, Ali Sedghi, Niloofar Kianifar, Hamidreza Kiani, Mohammad A. Khalesi, Maryam Derafshi, Raheleh |
author_facet | Jafari, Seyed A. Alami, Ali Sedghi, Niloofar Kianifar, Hamidreza Kiani, Mohammad A. Khalesi, Maryam Derafshi, Raheleh |
author_sort | Jafari, Seyed A. |
collection | PubMed |
description | BACKGROUND: Celiac disease (CD) is an autoimmune enteropathy that is caused by the intake of gluten-containing grains in genetically susceptible humans. The gliadin and glutenin parts of wheat gluten are the essential factors that cause intestinal damage. OBJECTIVES: We analyzed the performance of a time-resolved immunofluorometric assay (TR-IFMA) in the diagnosis of CD in children. For this purpose, we compared the performance of IgA anti-tissue transglutaminase antibodies (IgA anti-TTG) and IgG antibodies against deamidated gliadin peptides (IgG anti-DGP) for the diagnosis of CD. MATERIALS AND METHODS: In this cross-sectional study conducted in 2021 for a duration of about 6 months, 200 patients with suspected CD symptoms, children who needed screening due to Down syndrome or Turner syndrome, and the first-degree relatives of CD patients who underwent diagnostic evaluation were enrolled in a census study. RESULTS: This study compares existing point-of-care anti-DGP Ab (IgG) and anti-TTG Ab (IgA) tests against each other using the gold standard of duodenal biopsy and pathology. Serology as a screening test was acceptable (93.6% for anti-DGP vs. 94.2% for anti-TTG) for both of them. This equivalent sensitivity of serum TTG and the DGP tests validates its potential as a basic tool for serological testing. Furthermore, endoscopy is carried out in patients positive for both. CONCLUSIONS: Our study showed that for the diagnosis of CD, anti-DGP antibodies had comparable characteristics with anti-TTG (IgA) in terms of diagnostic specificity and sensitivity. Specify of anti-DGP was higher than that of anti-TTG. |
format | Online Article Text |
id | pubmed-10071923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-100719232023-04-05 Diagnostic accuracy of anti-DGP (IgG) for celiac disease Jafari, Seyed A. Alami, Ali Sedghi, Niloofar Kianifar, Hamidreza Kiani, Mohammad A. Khalesi, Maryam Derafshi, Raheleh J Family Med Prim Care Original Article BACKGROUND: Celiac disease (CD) is an autoimmune enteropathy that is caused by the intake of gluten-containing grains in genetically susceptible humans. The gliadin and glutenin parts of wheat gluten are the essential factors that cause intestinal damage. OBJECTIVES: We analyzed the performance of a time-resolved immunofluorometric assay (TR-IFMA) in the diagnosis of CD in children. For this purpose, we compared the performance of IgA anti-tissue transglutaminase antibodies (IgA anti-TTG) and IgG antibodies against deamidated gliadin peptides (IgG anti-DGP) for the diagnosis of CD. MATERIALS AND METHODS: In this cross-sectional study conducted in 2021 for a duration of about 6 months, 200 patients with suspected CD symptoms, children who needed screening due to Down syndrome or Turner syndrome, and the first-degree relatives of CD patients who underwent diagnostic evaluation were enrolled in a census study. RESULTS: This study compares existing point-of-care anti-DGP Ab (IgG) and anti-TTG Ab (IgA) tests against each other using the gold standard of duodenal biopsy and pathology. Serology as a screening test was acceptable (93.6% for anti-DGP vs. 94.2% for anti-TTG) for both of them. This equivalent sensitivity of serum TTG and the DGP tests validates its potential as a basic tool for serological testing. Furthermore, endoscopy is carried out in patients positive for both. CONCLUSIONS: Our study showed that for the diagnosis of CD, anti-DGP antibodies had comparable characteristics with anti-TTG (IgA) in terms of diagnostic specificity and sensitivity. Specify of anti-DGP was higher than that of anti-TTG. Wolters Kluwer - Medknow 2023-01 2023-02-15 /pmc/articles/PMC10071923/ /pubmed/37025242 http://dx.doi.org/10.4103/jfmpc.jfmpc_326_22 Text en Copyright: © 2023 Journal of Family Medicine and Primary Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Jafari, Seyed A. Alami, Ali Sedghi, Niloofar Kianifar, Hamidreza Kiani, Mohammad A. Khalesi, Maryam Derafshi, Raheleh Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title | Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title_full | Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title_fullStr | Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title_full_unstemmed | Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title_short | Diagnostic accuracy of anti-DGP (IgG) for celiac disease |
title_sort | diagnostic accuracy of anti-dgp (igg) for celiac disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071923/ https://www.ncbi.nlm.nih.gov/pubmed/37025242 http://dx.doi.org/10.4103/jfmpc.jfmpc_326_22 |
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