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Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole
Non-steroidal anti-inflammatory drugs (NSAIDs) are the most common cause of hypersensitivity reactions, with pyrazolones the most frequent drugs inducing selective reactions. Immediate selective hypersensitivity to pyrazolones is thought to be mediated by specific-IgE. Sensitivity of in vitro diagno...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814906/ https://www.ncbi.nlm.nih.gov/pubmed/27030298 http://dx.doi.org/10.1038/srep23845 |
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author | Ariza, Adriana García-Martín, Elena Salas, María Montañez, María I. Mayorga, Cristobalina Blanca-Lopez, Natalia Andreu, Inmaculada Perkins, James Blanca, Miguel Agúndez, José A. G. Torres, María J. |
author_facet | Ariza, Adriana García-Martín, Elena Salas, María Montañez, María I. Mayorga, Cristobalina Blanca-Lopez, Natalia Andreu, Inmaculada Perkins, James Blanca, Miguel Agúndez, José A. G. Torres, María J. |
author_sort | Ariza, Adriana |
collection | PubMed |
description | Non-steroidal anti-inflammatory drugs (NSAIDs) are the most common cause of hypersensitivity reactions, with pyrazolones the most frequent drugs inducing selective reactions. Immediate selective hypersensitivity to pyrazolones is thought to be mediated by specific-IgE. Sensitivity of in vitro diagnostic tests is low and this may be due to the incomplete characterization of the structures involved. Here we investigated whether main metabolites of metamizole (dipyrone) in human could be involved in the immune response using the basophil activation test (BAT). We studied subjects with confirmed selective immediate hypersensitivity to metamizole and performed BAT with metamizole and its metabolites: 4-methylamino-antipyrine (MAA), 4-aminoantipyrine (AA), 4-acetylamino-antipyrine (AAA) and 4-formylamino-antipyrine (FAA). BAT results showed an increase of positive results from 37.5% to 62.5% using metamizole plus metabolites as compared with the BAT carried out only with the parent drug, demonstrating that metamizole metabolites have a role in the reaction and can induce specific basophil activation in patients with immediate hypersensitivity to this drug. Our findings indicate that pyrazolone metabolites are useful for improving the in vitro diagnosis of allergic reactions to metamizole. |
format | Online Article Text |
id | pubmed-4814906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48149062016-04-04 Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole Ariza, Adriana García-Martín, Elena Salas, María Montañez, María I. Mayorga, Cristobalina Blanca-Lopez, Natalia Andreu, Inmaculada Perkins, James Blanca, Miguel Agúndez, José A. G. Torres, María J. Sci Rep Article Non-steroidal anti-inflammatory drugs (NSAIDs) are the most common cause of hypersensitivity reactions, with pyrazolones the most frequent drugs inducing selective reactions. Immediate selective hypersensitivity to pyrazolones is thought to be mediated by specific-IgE. Sensitivity of in vitro diagnostic tests is low and this may be due to the incomplete characterization of the structures involved. Here we investigated whether main metabolites of metamizole (dipyrone) in human could be involved in the immune response using the basophil activation test (BAT). We studied subjects with confirmed selective immediate hypersensitivity to metamizole and performed BAT with metamizole and its metabolites: 4-methylamino-antipyrine (MAA), 4-aminoantipyrine (AA), 4-acetylamino-antipyrine (AAA) and 4-formylamino-antipyrine (FAA). BAT results showed an increase of positive results from 37.5% to 62.5% using metamizole plus metabolites as compared with the BAT carried out only with the parent drug, demonstrating that metamizole metabolites have a role in the reaction and can induce specific basophil activation in patients with immediate hypersensitivity to this drug. Our findings indicate that pyrazolone metabolites are useful for improving the in vitro diagnosis of allergic reactions to metamizole. Nature Publishing Group 2016-03-31 /pmc/articles/PMC4814906/ /pubmed/27030298 http://dx.doi.org/10.1038/srep23845 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ariza, Adriana García-Martín, Elena Salas, María Montañez, María I. Mayorga, Cristobalina Blanca-Lopez, Natalia Andreu, Inmaculada Perkins, James Blanca, Miguel Agúndez, José A. G. Torres, María J. Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title | Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title_full | Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title_fullStr | Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title_full_unstemmed | Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title_short | Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
title_sort | pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814906/ https://www.ncbi.nlm.nih.gov/pubmed/27030298 http://dx.doi.org/10.1038/srep23845 |
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