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The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata
BACKGROUND: Alopecia areata (AA) is a noncicatricial (nonscarring) alopecia. The association between AA and celiac disease (CD) is debatable. Several studies declare the relationship between AA and CD as measurement of celiac autoantibodies (anti-gliadin IgA and anti-gliadin IgG), but a few studies...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036277/ https://www.ncbi.nlm.nih.gov/pubmed/27833723 http://dx.doi.org/10.4103/2008-7802.190607 |
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author | Mokhtari, Fatemeh Panjehpour, Tayebeh Naeini, Farahnaz Fatemi Hosseini, Sayed Mohsen Nilforoushzadeh, Mohammad Ali Matin, Marzieh |
author_facet | Mokhtari, Fatemeh Panjehpour, Tayebeh Naeini, Farahnaz Fatemi Hosseini, Sayed Mohsen Nilforoushzadeh, Mohammad Ali Matin, Marzieh |
author_sort | Mokhtari, Fatemeh |
collection | PubMed |
description | BACKGROUND: Alopecia areata (AA) is a noncicatricial (nonscarring) alopecia. The association between AA and celiac disease (CD) is debatable. Several studies declare the relationship between AA and CD as measurement of celiac autoantibodies (anti-gliadin IgA and anti-gliadin IgG), but a few studies consider anti-tissue transglutaminase IgA. The aim of this study was to evaluate the frequency distribution of celiac autoantibodies (all of them) in patients with AA compared with controls. METHODS: This study is a case–control study. Thirty-five patients entered in each group. Anti-gliadin IgA, anti-gliadin IgG, and anti-tissue transglutaminase IgA were tested in all patients. Samples were examined in ELISA method with binding site's kits, and the result was reported as positive/negative. Finally, the frequency distribution of autoantibodies was examined. RESULTS: The age average did not show a significant difference between two groups (P = 0.62). In addition, there was no significant difference between the two groups based on gender (P = 0.15). The prevalence of antibody in case and control groups was 2.85% and 0%, respectively. There was no significant difference between the two groups (P = 0.31). CONCLUSIONS: There may be a relationship between CD and AA, but the absence of statistical association between AA and CD does not mean that there is no relationship between gluten and AA in certain patients. Thus, we have shown here that the biological tests to search for CD do not bring information and proof enough, and it is why we recommend another approach to disclose gluten intolerance in AA patients. |
format | Online Article Text |
id | pubmed-5036277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50362772016-11-10 The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata Mokhtari, Fatemeh Panjehpour, Tayebeh Naeini, Farahnaz Fatemi Hosseini, Sayed Mohsen Nilforoushzadeh, Mohammad Ali Matin, Marzieh Int J Prev Med Original Article BACKGROUND: Alopecia areata (AA) is a noncicatricial (nonscarring) alopecia. The association between AA and celiac disease (CD) is debatable. Several studies declare the relationship between AA and CD as measurement of celiac autoantibodies (anti-gliadin IgA and anti-gliadin IgG), but a few studies consider anti-tissue transglutaminase IgA. The aim of this study was to evaluate the frequency distribution of celiac autoantibodies (all of them) in patients with AA compared with controls. METHODS: This study is a case–control study. Thirty-five patients entered in each group. Anti-gliadin IgA, anti-gliadin IgG, and anti-tissue transglutaminase IgA were tested in all patients. Samples were examined in ELISA method with binding site's kits, and the result was reported as positive/negative. Finally, the frequency distribution of autoantibodies was examined. RESULTS: The age average did not show a significant difference between two groups (P = 0.62). In addition, there was no significant difference between the two groups based on gender (P = 0.15). The prevalence of antibody in case and control groups was 2.85% and 0%, respectively. There was no significant difference between the two groups (P = 0.31). CONCLUSIONS: There may be a relationship between CD and AA, but the absence of statistical association between AA and CD does not mean that there is no relationship between gluten and AA in certain patients. Thus, we have shown here that the biological tests to search for CD do not bring information and proof enough, and it is why we recommend another approach to disclose gluten intolerance in AA patients. Medknow Publications & Media Pvt Ltd 2016-09-14 /pmc/articles/PMC5036277/ /pubmed/27833723 http://dx.doi.org/10.4103/2008-7802.190607 Text en Copyright: © 2016 International Journal of Preventive Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Mokhtari, Fatemeh Panjehpour, Tayebeh Naeini, Farahnaz Fatemi Hosseini, Sayed Mohsen Nilforoushzadeh, Mohammad Ali Matin, Marzieh The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title | The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title_full | The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title_fullStr | The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title_full_unstemmed | The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title_short | The Frequency Distribution of Celiac Autoantibodies in Alopecia Areata |
title_sort | frequency distribution of celiac autoantibodies in alopecia areata |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036277/ https://www.ncbi.nlm.nih.gov/pubmed/27833723 http://dx.doi.org/10.4103/2008-7802.190607 |
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