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Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease
AIM: Deamidated gliadin peptide‐IgG (DGP‐IgG) antibody serology testing is widely utilised in screening for coeliac disease in Australia; however, it is used sparingly in Europe. The aim of this study was to assess the diagnostic value of a positive DGP‐IgG in the setting of a negative tissue transg...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley & Sons Australia, Ltd.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545789/ https://www.ncbi.nlm.nih.gov/pubmed/35726522 http://dx.doi.org/10.1111/jpc.16071 |
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author | Vootukuru, Nikil Singh, Harveen Giles, Edward |
author_facet | Vootukuru, Nikil Singh, Harveen Giles, Edward |
author_sort | Vootukuru, Nikil |
collection | PubMed |
description | AIM: Deamidated gliadin peptide‐IgG (DGP‐IgG) antibody serology testing is widely utilised in screening for coeliac disease in Australia; however, it is used sparingly in Europe. The aim of this study was to assess the diagnostic value of a positive DGP‐IgG in the setting of a negative tissue transglutaminase‐IgA (tTG‐IgA) for gastrointestinal pathology among paediatric patients. METHODS: We conducted a retrospective cohort study of all children with an elevated DGP‐IgG in the setting of a negative tTG‐IgA who underwent gastroscopy over a 48‐month period (January 2015–December 2018) at a tertiary paediatric centre. They were identified utilising the electronic pathology database and demographic and clinical data were collected from electronic medical records. Patients who had previously been diagnosed with coeliac disease were on a gluten‐free diet or over the age of 18 were excluded from the study. RESULTS: Twenty‐six patients with an elevated DGP‐IgG in the setting of a negative tTG‐IgA underwent gastroscopy. Our study yielded a positive predictive value of 1/26 (3.9% CI 95% 0.7%, 18.9%) for the diagnosis of coeliac disease. Overall, there were 25 histopathological diagnoses including 1 diagnosis of coeliac disease among the total 26 patients who were positive DGP‐IgG and negative tTG‐IgA and underwent gastroscopy. CONCLUSIONS: Our findings suggest that an isolated positive DGP‐IgG has a very low diagnostic yield for coeliac disease in children and may be indicative of other gastrointestinal pathology. |
format | Online Article Text |
id | pubmed-9545789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95457892022-10-14 Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease Vootukuru, Nikil Singh, Harveen Giles, Edward J Paediatr Child Health Original Articles AIM: Deamidated gliadin peptide‐IgG (DGP‐IgG) antibody serology testing is widely utilised in screening for coeliac disease in Australia; however, it is used sparingly in Europe. The aim of this study was to assess the diagnostic value of a positive DGP‐IgG in the setting of a negative tissue transglutaminase‐IgA (tTG‐IgA) for gastrointestinal pathology among paediatric patients. METHODS: We conducted a retrospective cohort study of all children with an elevated DGP‐IgG in the setting of a negative tTG‐IgA who underwent gastroscopy over a 48‐month period (January 2015–December 2018) at a tertiary paediatric centre. They were identified utilising the electronic pathology database and demographic and clinical data were collected from electronic medical records. Patients who had previously been diagnosed with coeliac disease were on a gluten‐free diet or over the age of 18 were excluded from the study. RESULTS: Twenty‐six patients with an elevated DGP‐IgG in the setting of a negative tTG‐IgA underwent gastroscopy. Our study yielded a positive predictive value of 1/26 (3.9% CI 95% 0.7%, 18.9%) for the diagnosis of coeliac disease. Overall, there were 25 histopathological diagnoses including 1 diagnosis of coeliac disease among the total 26 patients who were positive DGP‐IgG and negative tTG‐IgA and underwent gastroscopy. CONCLUSIONS: Our findings suggest that an isolated positive DGP‐IgG has a very low diagnostic yield for coeliac disease in children and may be indicative of other gastrointestinal pathology. John Wiley & Sons Australia, Ltd. 2022-06-21 2022-09 /pmc/articles/PMC9545789/ /pubmed/35726522 http://dx.doi.org/10.1111/jpc.16071 Text en © 2022 The Authors. Journal of Paediatrics and Child Health published by John Wiley & Sons Australia, Ltd on behalf of Paediatrics and Child Health Division (The Royal Australasian College of Physicians). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Vootukuru, Nikil Singh, Harveen Giles, Edward Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title | Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title_full | Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title_fullStr | Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title_full_unstemmed | Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title_short | Isolated positive deamidated gliadin peptide‐IgG has limited diagnostic utility in coeliac disease |
title_sort | isolated positive deamidated gliadin peptide‐igg has limited diagnostic utility in coeliac disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545789/ https://www.ncbi.nlm.nih.gov/pubmed/35726522 http://dx.doi.org/10.1111/jpc.16071 |
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