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Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase?
BACKGROUND: It is hypothesized that because of higher mast cell numbers and mediator release, mastocytosis predisposes patients for systemic immediate-type hypersensitivity reactions to certain drugs including non-steroidal anti-inflammatory drugs (NSAID). OBJECTIVE: To clarify whether patients with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002884/ https://www.ncbi.nlm.nih.gov/pubmed/24782901 http://dx.doi.org/10.1186/1710-1492-10-19 |
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author | Seitz, Cornelia S Brockow, Knut Hain, Johannes Trautmann, Axel |
author_facet | Seitz, Cornelia S Brockow, Knut Hain, Johannes Trautmann, Axel |
author_sort | Seitz, Cornelia S |
collection | PubMed |
description | BACKGROUND: It is hypothesized that because of higher mast cell numbers and mediator release, mastocytosis predisposes patients for systemic immediate-type hypersensitivity reactions to certain drugs including non-steroidal anti-inflammatory drugs (NSAID). OBJECTIVE: To clarify whether patients with NSAID hypersensitivity show increased basal serum tryptase levels as sign for underlying mast cell disease. METHODS: As part of our allergy work-up, basal serum tryptase levels were determined in all patients with a diagnosis of NSAID hypersensitivity and the severity of the reaction was graded. Patients with confirmed IgE-mediated hymenoptera venom allergy served as a comparison group. RESULTS: Out of 284 patients with NSAID hypersensitivity, 26 were identified with basal serum tryptase > 10.0 ng/mL (9.2%). In contrast, significantly (P = .004) more hymenoptera venom allergic patients had elevated tryptase > 10.0 ng/mL (83 out of 484; 17.1%). Basal tryptase > 20.0 ng/mL was indicative for severe anaphylaxis only in venom allergic subjects (29 patients; 4x grade 2 and 25x grade 3 anaphylaxis), but not in NSAID hypersensitive patients (6 patients; 4x grade 1, 2x grade 2). CONCLUSIONS: In contrast to hymenoptera venom allergy, NSAID hypersensitivity do not seem to be associated with elevated basal serum tryptase levels and levels > 20 ng/mL were not related to increased severity of the clinical reaction. This suggests that mastocytosis patients may be treated with NSAID without special precautions. |
format | Online Article Text |
id | pubmed-4002884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40028842014-04-30 Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? Seitz, Cornelia S Brockow, Knut Hain, Johannes Trautmann, Axel Allergy Asthma Clin Immunol Research BACKGROUND: It is hypothesized that because of higher mast cell numbers and mediator release, mastocytosis predisposes patients for systemic immediate-type hypersensitivity reactions to certain drugs including non-steroidal anti-inflammatory drugs (NSAID). OBJECTIVE: To clarify whether patients with NSAID hypersensitivity show increased basal serum tryptase levels as sign for underlying mast cell disease. METHODS: As part of our allergy work-up, basal serum tryptase levels were determined in all patients with a diagnosis of NSAID hypersensitivity and the severity of the reaction was graded. Patients with confirmed IgE-mediated hymenoptera venom allergy served as a comparison group. RESULTS: Out of 284 patients with NSAID hypersensitivity, 26 were identified with basal serum tryptase > 10.0 ng/mL (9.2%). In contrast, significantly (P = .004) more hymenoptera venom allergic patients had elevated tryptase > 10.0 ng/mL (83 out of 484; 17.1%). Basal tryptase > 20.0 ng/mL was indicative for severe anaphylaxis only in venom allergic subjects (29 patients; 4x grade 2 and 25x grade 3 anaphylaxis), but not in NSAID hypersensitive patients (6 patients; 4x grade 1, 2x grade 2). CONCLUSIONS: In contrast to hymenoptera venom allergy, NSAID hypersensitivity do not seem to be associated with elevated basal serum tryptase levels and levels > 20 ng/mL were not related to increased severity of the clinical reaction. This suggests that mastocytosis patients may be treated with NSAID without special precautions. BioMed Central 2014-04-24 /pmc/articles/PMC4002884/ /pubmed/24782901 http://dx.doi.org/10.1186/1710-1492-10-19 Text en Copyright © 2014 Seitz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Seitz, Cornelia S Brockow, Knut Hain, Johannes Trautmann, Axel Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title | Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title_full | Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title_fullStr | Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title_full_unstemmed | Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title_short | Non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
title_sort | non-steroidal anti-inflammatory drug hypersensitivity: association with elevated basal serum tryptase? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002884/ https://www.ncbi.nlm.nih.gov/pubmed/24782901 http://dx.doi.org/10.1186/1710-1492-10-19 |
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