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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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.
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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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