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Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients
BACKGROUND: Profilin sensitisation is considered a diagnostic confounding factor in areas where patients are exposed to multiple pollens. The aim of this study is to assess pollen sensitisation profiles in adults and children and to evaluate, by means of component-resolved diagnosis (CRD) and skin p...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926298/ https://www.ncbi.nlm.nih.gov/pubmed/27358726 http://dx.doi.org/10.1186/s13601-016-0114-y |
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author | Segura, Nieves Abos, Teresa Compaired, José A. Compés, Esther Guallar, Isabel Morales, Manuel Monzón, Susana Mozota, José Muñoz, Pilar Pola, Jesús Quintana, Macarena Rojas, Beatriz Juan, Sara San Villa, Felicitas Zapata, Cristina Jimeno, Lucía de la Torre, Fernando |
author_facet | Segura, Nieves Abos, Teresa Compaired, José A. Compés, Esther Guallar, Isabel Morales, Manuel Monzón, Susana Mozota, José Muñoz, Pilar Pola, Jesús Quintana, Macarena Rojas, Beatriz Juan, Sara San Villa, Felicitas Zapata, Cristina Jimeno, Lucía de la Torre, Fernando |
author_sort | Segura, Nieves |
collection | PubMed |
description | BACKGROUND: Profilin sensitisation is considered a diagnostic confounding factor in areas where patients are exposed to multiple pollens. The aim of this study is to assess pollen sensitisation profiles in adults and children and to evaluate, by means of component-resolved diagnosis (CRD) and skin prick testing (SPT), which pollens may be considered as risk factors of profilin sensitisation in order to establish the best diagnostic approach in polysensitised patients. METHODS: A total of 231 pollen-allergic patients (adults and children) were included, out of the pollen season, from an area with similar levels of pollen exposure. Allergological diagnosis was performed by SPT and determination of specific IgE (sIgE) to major allergen components (ADVIA-Centaur™). Patients had not received immunotherapy in the last 5 years and had to reside in the area for 5 consecutive years before entering the study. RESULTS: The relation between sensitisation measured by SPT and by sIgE was studied using a model of cases (patients with +sIgE to a specific allergen) and controls (patients with −sIgE to the same allergen). The outcome, in terms of odds-ratios (OR), was statistically significant for Olea (Ole e 1) (p = 0.0005), Salsola (Sal k 1) (p = 0.0118) and Platanus (Pla a 1+ 2) (p = 0.0372). While positivity of SPT to most pollens was statistically associated with a risk of profilin sensitisation, by CRD the association was statistically significant only for Ole e 1 (OR 3.5, CI 95 %, 1.6–7.6, p = 0.0014), and Phl p 5 (OR 11.9, CI 95 %, 4.1–35.2, p < 0.001). When analysing this association using a logistic regression model, Phl p 5 was the only allergen associated with the risk of being sensitised to profilin (p = 0.0023). CONCLUSIONS: In patients sensitised to profilin, the concordance between SPT and CRD is much lower than in those not sensitised to profilin. CRD is able to provide refined information about which pollens increase the risk of sensitisation to profilin. |
format | Online Article Text |
id | pubmed-4926298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49262982016-06-29 Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients Segura, Nieves Abos, Teresa Compaired, José A. Compés, Esther Guallar, Isabel Morales, Manuel Monzón, Susana Mozota, José Muñoz, Pilar Pola, Jesús Quintana, Macarena Rojas, Beatriz Juan, Sara San Villa, Felicitas Zapata, Cristina Jimeno, Lucía de la Torre, Fernando Clin Transl Allergy Research BACKGROUND: Profilin sensitisation is considered a diagnostic confounding factor in areas where patients are exposed to multiple pollens. The aim of this study is to assess pollen sensitisation profiles in adults and children and to evaluate, by means of component-resolved diagnosis (CRD) and skin prick testing (SPT), which pollens may be considered as risk factors of profilin sensitisation in order to establish the best diagnostic approach in polysensitised patients. METHODS: A total of 231 pollen-allergic patients (adults and children) were included, out of the pollen season, from an area with similar levels of pollen exposure. Allergological diagnosis was performed by SPT and determination of specific IgE (sIgE) to major allergen components (ADVIA-Centaur™). Patients had not received immunotherapy in the last 5 years and had to reside in the area for 5 consecutive years before entering the study. RESULTS: The relation between sensitisation measured by SPT and by sIgE was studied using a model of cases (patients with +sIgE to a specific allergen) and controls (patients with −sIgE to the same allergen). The outcome, in terms of odds-ratios (OR), was statistically significant for Olea (Ole e 1) (p = 0.0005), Salsola (Sal k 1) (p = 0.0118) and Platanus (Pla a 1+ 2) (p = 0.0372). While positivity of SPT to most pollens was statistically associated with a risk of profilin sensitisation, by CRD the association was statistically significant only for Ole e 1 (OR 3.5, CI 95 %, 1.6–7.6, p = 0.0014), and Phl p 5 (OR 11.9, CI 95 %, 4.1–35.2, p < 0.001). When analysing this association using a logistic regression model, Phl p 5 was the only allergen associated with the risk of being sensitised to profilin (p = 0.0023). CONCLUSIONS: In patients sensitised to profilin, the concordance between SPT and CRD is much lower than in those not sensitised to profilin. CRD is able to provide refined information about which pollens increase the risk of sensitisation to profilin. BioMed Central 2016-06-29 /pmc/articles/PMC4926298/ /pubmed/27358726 http://dx.doi.org/10.1186/s13601-016-0114-y Text en © de la Torre et al 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Segura, Nieves Abos, Teresa Compaired, José A. Compés, Esther Guallar, Isabel Morales, Manuel Monzón, Susana Mozota, José Muñoz, Pilar Pola, Jesús Quintana, Macarena Rojas, Beatriz Juan, Sara San Villa, Felicitas Zapata, Cristina Jimeno, Lucía de la Torre, Fernando Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title | Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title_full | Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title_fullStr | Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title_full_unstemmed | Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title_short | Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients |
title_sort | influence of profilin on sensitisation profiles determined by cutaneous tests and ige to major allergens in polysensitised patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926298/ https://www.ncbi.nlm.nih.gov/pubmed/27358726 http://dx.doi.org/10.1186/s13601-016-0114-y |
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