Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis

Members of the interleukin-1 (IL-1) family are implicated in the pathogenesis of sarcoidosis and idiopathic pulmonary fibrosis (IPF). We have, therefore, performed a case-control study to investigate a plausible association between sarcoidosis and the polymorphisms in the IL-1alpha, IL-1beta, and IL...

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Veröffentlicht in:American journal of respiratory and critical care medicine 2002-01, Vol.165 (2), p.148-151
Hauptverfasser: HUTYROVA, BEATA, PANTELIDIS, PANAGIOTIS, DRABEK, JIRI, ZURKOVA, MONIKA, KOLEK, VITEZSLAV, LENHART, KAREL, WELSH, KENNETH I, DU BOIS, ROLAND M, PETREK, MARTIN
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container_issue 2
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container_title American journal of respiratory and critical care medicine
container_volume 165
creator HUTYROVA, BEATA
PANTELIDIS, PANAGIOTIS
DRABEK, JIRI
ZURKOVA, MONIKA
KOLEK, VITEZSLAV
LENHART, KAREL
WELSH, KENNETH I
DU BOIS, ROLAND M
PETREK, MARTIN
description Members of the interleukin-1 (IL-1) family are implicated in the pathogenesis of sarcoidosis and idiopathic pulmonary fibrosis (IPF). We have, therefore, performed a case-control study to investigate a plausible association between sarcoidosis and the polymorphisms in the IL-1alpha, IL-1beta, and IL-1 receptor antagonist (IL-1Ra) genes. Further, as a separate question, we explored whether the aforementioned genes of the IL-1 cluster are associated with IPF. Using PCR with sequence-specific primers, IL-1alpha -889, IL-1beta -511, IL-1beta +3953, and IL-1Ra intron 2 VNTR polymorphisms were determined in 348 white subjects of West Slavonic ancestry (95 patients with sarcoidosis, 54 patients with IPF, and 199 healthy control subjects). The IL-1alpha -889 1.1 genotype was significantly overrepresented in patients with sarcoidosis in comparison with control subjects (60.0 versus 44.2%, p = 0.012, p(corr) = 0.047). The distribution of IL-1beta -511, IL-1beta +3953, and IL-1Ra VNTR genotypes and alleles did not significantly differ between the cases and controls. No association between IPF and the investigated polymorphisms was found. Strong linkage disequilibrium between pairs of polymorphic loci was observed. Further population studies are warranted to confirm the observed association between sarcoidosis and the IL-1alpha polymorphism and also to explore mechanisms of IL-1alpha -889 participation in aberrant immune response in sarcoidosis.
doi_str_mv 10.1164/ajrccm.165.2.2106004
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We have, therefore, performed a case-control study to investigate a plausible association between sarcoidosis and the polymorphisms in the IL-1alpha, IL-1beta, and IL-1 receptor antagonist (IL-1Ra) genes. Further, as a separate question, we explored whether the aforementioned genes of the IL-1 cluster are associated with IPF. Using PCR with sequence-specific primers, IL-1alpha -889, IL-1beta -511, IL-1beta +3953, and IL-1Ra intron 2 VNTR polymorphisms were determined in 348 white subjects of West Slavonic ancestry (95 patients with sarcoidosis, 54 patients with IPF, and 199 healthy control subjects). The IL-1alpha -889 1.1 genotype was significantly overrepresented in patients with sarcoidosis in comparison with control subjects (60.0 versus 44.2%, p = 0.012, p(corr) = 0.047). The distribution of IL-1beta -511, IL-1beta +3953, and IL-1Ra VNTR genotypes and alleles did not significantly differ between the cases and controls. No association between IPF and the investigated polymorphisms was found. Strong linkage disequilibrium between pairs of polymorphic loci was observed. Further population studies are warranted to confirm the observed association between sarcoidosis and the IL-1alpha polymorphism and also to explore mechanisms of IL-1alpha -889 participation in aberrant immune response in sarcoidosis.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/ajrccm.165.2.2106004</identifier><identifier>PMID: 11790645</identifier><language>eng</language><publisher>New York, NY: Am Thoracic Soc</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Case-Control Studies ; Female ; Gene Expression - genetics ; Gene Frequency - genetics ; Humans ; Interleukin-1 - genetics ; Linkage Disequilibrium - genetics ; Male ; Medical sciences ; Middle Aged ; Multigene Family - genetics ; Pneumology ; Polymerase Chain Reaction ; Polymorphism, Genetic - genetics ; Pulmonary Fibrosis - genetics ; Receptors, Interleukin-1 - antagonists &amp; inhibitors ; Receptors, Interleukin-1 - genetics ; Respiratory system : syndromes and miscellaneous diseases ; Sarcoidosis, Pulmonary - genetics ; Sarcoidosis. 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We have, therefore, performed a case-control study to investigate a plausible association between sarcoidosis and the polymorphisms in the IL-1alpha, IL-1beta, and IL-1 receptor antagonist (IL-1Ra) genes. Further, as a separate question, we explored whether the aforementioned genes of the IL-1 cluster are associated with IPF. Using PCR with sequence-specific primers, IL-1alpha -889, IL-1beta -511, IL-1beta +3953, and IL-1Ra intron 2 VNTR polymorphisms were determined in 348 white subjects of West Slavonic ancestry (95 patients with sarcoidosis, 54 patients with IPF, and 199 healthy control subjects). The IL-1alpha -889 1.1 genotype was significantly overrepresented in patients with sarcoidosis in comparison with control subjects (60.0 versus 44.2%, p = 0.012, p(corr) = 0.047). The distribution of IL-1beta -511, IL-1beta +3953, and IL-1Ra VNTR genotypes and alleles did not significantly differ between the cases and controls. No association between IPF and the investigated polymorphisms was found. Strong linkage disequilibrium between pairs of polymorphic loci was observed. 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No association between IPF and the investigated polymorphisms was found. Strong linkage disequilibrium between pairs of polymorphic loci was observed. Further population studies are warranted to confirm the observed association between sarcoidosis and the IL-1alpha polymorphism and also to explore mechanisms of IL-1alpha -889 participation in aberrant immune response in sarcoidosis.</abstract><cop>New York, NY</cop><pub>Am Thoracic Soc</pub><pmid>11790645</pmid><doi>10.1164/ajrccm.165.2.2106004</doi><tpages>4</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete; American Thoracic Society (ATS) Journals Online; EZB-FREE-00999 freely available EZB journals
subjects Adolescent
Adult
Aged
Biological and medical sciences
Case-Control Studies
Female
Gene Expression - genetics
Gene Frequency - genetics
Humans
Interleukin-1 - genetics
Linkage Disequilibrium - genetics
Male
Medical sciences
Middle Aged
Multigene Family - genetics
Pneumology
Polymerase Chain Reaction
Polymorphism, Genetic - genetics
Pulmonary Fibrosis - genetics
Receptors, Interleukin-1 - antagonists & inhibitors
Receptors, Interleukin-1 - genetics
Respiratory system : syndromes and miscellaneous diseases
Sarcoidosis, Pulmonary - genetics
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
title Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis
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