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Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort
BACKGROUND: FLG null variants of which 2282del4 and R501X are the most frequent in Caucasians are established risk factors for atopic dermatitis (AD) with an effect probably mediated through impairment of epidermal barrier. Among subjects with AD FLG defects are also consistently associated with ast...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041817/ https://www.ncbi.nlm.nih.gov/pubmed/21365004 http://dx.doi.org/10.1371/journal.pone.0016933 |
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author | Ponińska, Joanna Samoliński, Bolesław Tomaszewska, Aneta Raciborski, Filip Samel-Kowalik, Piotr Walkiewicz, Artur Lipiec, Agnieszka Piekarska, Barbara Komorowski, Jarosław Krzych-Fałta, Edyta Namysłowski, Andrzej Borowicz, Jacek Kostrzewa, Grażyna Majewski, Sławomir Płoski, Rafał |
author_facet | Ponińska, Joanna Samoliński, Bolesław Tomaszewska, Aneta Raciborski, Filip Samel-Kowalik, Piotr Walkiewicz, Artur Lipiec, Agnieszka Piekarska, Barbara Komorowski, Jarosław Krzych-Fałta, Edyta Namysłowski, Andrzej Borowicz, Jacek Kostrzewa, Grażyna Majewski, Sławomir Płoski, Rafał |
author_sort | Ponińska, Joanna |
collection | PubMed |
description | BACKGROUND: FLG null variants of which 2282del4 and R501X are the most frequent in Caucasians are established risk factors for atopic dermatitis (AD) with an effect probably mediated through impairment of epidermal barrier. Among subjects with AD FLG defects are also consistently associated with asthma and allergic rhinitis (AR) but it is less clear to what extent these associations are also present independently from skin disease. The aim of the present study was to evaluate the role of 2282del4 and R501X in predisposing to these allergic phenotypes in a Polish population. METHODOLOGY: 2282del4 and R501X were typed among 3,802 participants of the Epidemiology of Allergic Diseases in Poland (ECAP) survey, a cross-sectional population-based study using ECRHS II and ISAAC questionnaires, and ambulatory examination. PRINCIPAL FINDINGS: The FLG null variants were associated with AD (OR = 2.01, CI: 1.20–3.36, P = 0.007), allergic rhinitis (in particular persistent form, OR = 1.69, CI:1.12–2.54, P = 0.011), and asthma (in particular atopic asthma, OR = 2.22, CI:1.24–3.96, P = 0.006). Association with atopic asthma (but not persistent allergic rhinitis) was also present in the absence of AD, (OR = 2.02, CI: 1.07–3.81, P = 0.027) as well as in the absence of AD and history of broadly defined inflammatory skin disease (OR = 2.30, CI: 1.07–4.93, P = 0.03). Association to atopic asthma would have not been found if diagnosis was made by questionnaire only (OR = 1.15, CI: 0.58–2.32, P = 0.8). We did not observe an association between FLG variants and allergic sensitizations (P = 0.8) or total IgE. (P = 0.6). CONCLUSIONS/SIGNIFICANCE: In a Polish population FLG 2282del4 and R501X carriage increases risk for development of AD and atopic asthma (also in the absence of AD or history thereof). This suggests that interventions aimed at restoring epidermal barrier may have a general role in asthma prophylaxis/treatment. |
format | Text |
id | pubmed-3041817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30418172011-03-01 Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort Ponińska, Joanna Samoliński, Bolesław Tomaszewska, Aneta Raciborski, Filip Samel-Kowalik, Piotr Walkiewicz, Artur Lipiec, Agnieszka Piekarska, Barbara Komorowski, Jarosław Krzych-Fałta, Edyta Namysłowski, Andrzej Borowicz, Jacek Kostrzewa, Grażyna Majewski, Sławomir Płoski, Rafał PLoS One Research Article BACKGROUND: FLG null variants of which 2282del4 and R501X are the most frequent in Caucasians are established risk factors for atopic dermatitis (AD) with an effect probably mediated through impairment of epidermal barrier. Among subjects with AD FLG defects are also consistently associated with asthma and allergic rhinitis (AR) but it is less clear to what extent these associations are also present independently from skin disease. The aim of the present study was to evaluate the role of 2282del4 and R501X in predisposing to these allergic phenotypes in a Polish population. METHODOLOGY: 2282del4 and R501X were typed among 3,802 participants of the Epidemiology of Allergic Diseases in Poland (ECAP) survey, a cross-sectional population-based study using ECRHS II and ISAAC questionnaires, and ambulatory examination. PRINCIPAL FINDINGS: The FLG null variants were associated with AD (OR = 2.01, CI: 1.20–3.36, P = 0.007), allergic rhinitis (in particular persistent form, OR = 1.69, CI:1.12–2.54, P = 0.011), and asthma (in particular atopic asthma, OR = 2.22, CI:1.24–3.96, P = 0.006). Association with atopic asthma (but not persistent allergic rhinitis) was also present in the absence of AD, (OR = 2.02, CI: 1.07–3.81, P = 0.027) as well as in the absence of AD and history of broadly defined inflammatory skin disease (OR = 2.30, CI: 1.07–4.93, P = 0.03). Association to atopic asthma would have not been found if diagnosis was made by questionnaire only (OR = 1.15, CI: 0.58–2.32, P = 0.8). We did not observe an association between FLG variants and allergic sensitizations (P = 0.8) or total IgE. (P = 0.6). CONCLUSIONS/SIGNIFICANCE: In a Polish population FLG 2282del4 and R501X carriage increases risk for development of AD and atopic asthma (also in the absence of AD or history thereof). This suggests that interventions aimed at restoring epidermal barrier may have a general role in asthma prophylaxis/treatment. Public Library of Science 2011-02-18 /pmc/articles/PMC3041817/ /pubmed/21365004 http://dx.doi.org/10.1371/journal.pone.0016933 Text en Ponińska et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ponińska, Joanna Samoliński, Bolesław Tomaszewska, Aneta Raciborski, Filip Samel-Kowalik, Piotr Walkiewicz, Artur Lipiec, Agnieszka Piekarska, Barbara Komorowski, Jarosław Krzych-Fałta, Edyta Namysłowski, Andrzej Borowicz, Jacek Kostrzewa, Grażyna Majewski, Sławomir Płoski, Rafał Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title | Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title_full | Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title_fullStr | Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title_full_unstemmed | Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title_short | Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort |
title_sort | filaggrin gene defects are independent risk factors for atopic asthma in a polish population: a study in ecap cohort |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041817/ https://www.ncbi.nlm.nih.gov/pubmed/21365004 http://dx.doi.org/10.1371/journal.pone.0016933 |
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