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 |
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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 & 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</subject><ispartof>American journal of respiratory and critical care medicine, 2002-01, Vol.165 (2), p.148-151</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-52fc731bb2769d546319c21142dcf1d36f7071b3f4669b77d6e10610e5851dd63</citedby><cites>FETCH-LOGICAL-c282t-52fc731bb2769d546319c21142dcf1d36f7071b3f4669b77d6e10610e5851dd63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4025,4026,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13463793$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11790645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HUTYROVA, BEATA</creatorcontrib><creatorcontrib>PANTELIDIS, PANAGIOTIS</creatorcontrib><creatorcontrib>DRABEK, JIRI</creatorcontrib><creatorcontrib>ZURKOVA, MONIKA</creatorcontrib><creatorcontrib>KOLEK, VITEZSLAV</creatorcontrib><creatorcontrib>LENHART, KAREL</creatorcontrib><creatorcontrib>WELSH, KENNETH I</creatorcontrib><creatorcontrib>DU BOIS, ROLAND M</creatorcontrib><creatorcontrib>PETREK, MARTIN</creatorcontrib><title>Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Gene Expression - genetics</subject><subject>Gene Frequency - genetics</subject><subject>Humans</subject><subject>Interleukin-1 - genetics</subject><subject>Linkage Disequilibrium - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multigene Family - genetics</subject><subject>Pneumology</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Pulmonary Fibrosis - genetics</subject><subject>Receptors, Interleukin-1 - antagonists & inhibitors</subject><subject>Receptors, Interleukin-1 - genetics</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Sarcoidosis, Pulmonary - genetics</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkFtr3DAQRkVJaS7tPwhBLyn0wVuNrqvHsuSyEGigCbRPQpbkrBLZ3kprSv59FWzIkwZx5puZg9A5kBWA5N_tc3auX4EUK7qiQCQh_AM6AcFEw7UiR7UmijWc69_H6LSUZ0KAroF8QscAShPJxQn6sx0OIacwvcShAXwThoA3aSr1E9-P6bUf834XS19wHPAvm90Y_VhiwXbweOvjuLeHXXT4fkr9ONj8iq9jm9-Iz-hjZ1MJX5b3DD1eXz1sbpu7nzfbzY-7xtE1PTSCdk4xaFuqpPaCSwbaUQBOvevAM9kpoqBlHZdSt0p5GeqtQIJYC_BesjP0dc7d5_HvFMrB9LG4kJIdwjgVo4BpAZpXkM-gq_uVHDqzz7GvKxsg5k2pmZWaqtRQsyitbRdL_tT2wb83LQ4rcLkAtjibumwHF8s7x-pNSrPKfZu5XXza_Ys5mNLblGosLJPnwcDX7D8b046s</recordid><startdate>20020115</startdate><enddate>20020115</enddate><creator>HUTYROVA, BEATA</creator><creator>PANTELIDIS, PANAGIOTIS</creator><creator>DRABEK, JIRI</creator><creator>ZURKOVA, MONIKA</creator><creator>KOLEK, VITEZSLAV</creator><creator>LENHART, KAREL</creator><creator>WELSH, KENNETH I</creator><creator>DU BOIS, ROLAND M</creator><creator>PETREK, MARTIN</creator><general>Am Thoracic Soc</general><general>American Lung Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20020115</creationdate><title>Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis</title><author>HUTYROVA, BEATA ; PANTELIDIS, PANAGIOTIS ; DRABEK, JIRI ; ZURKOVA, MONIKA ; KOLEK, VITEZSLAV ; LENHART, KAREL ; WELSH, KENNETH I ; DU BOIS, ROLAND M ; PETREK, MARTIN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-52fc731bb2769d546319c21142dcf1d36f7071b3f4669b77d6e10610e5851dd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Gene Expression - genetics</topic><topic>Gene Frequency - genetics</topic><topic>Humans</topic><topic>Interleukin-1 - genetics</topic><topic>Linkage Disequilibrium - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multigene Family - genetics</topic><topic>Pneumology</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Pulmonary Fibrosis - genetics</topic><topic>Receptors, Interleukin-1 - antagonists & inhibitors</topic><topic>Receptors, Interleukin-1 - genetics</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Sarcoidosis, Pulmonary - genetics</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HUTYROVA, BEATA</creatorcontrib><creatorcontrib>PANTELIDIS, PANAGIOTIS</creatorcontrib><creatorcontrib>DRABEK, JIRI</creatorcontrib><creatorcontrib>ZURKOVA, MONIKA</creatorcontrib><creatorcontrib>KOLEK, VITEZSLAV</creatorcontrib><creatorcontrib>LENHART, KAREL</creatorcontrib><creatorcontrib>WELSH, KENNETH I</creatorcontrib><creatorcontrib>DU BOIS, ROLAND M</creatorcontrib><creatorcontrib>PETREK, MARTIN</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HUTYROVA, BEATA</au><au>PANTELIDIS, PANAGIOTIS</au><au>DRABEK, JIRI</au><au>ZURKOVA, MONIKA</au><au>KOLEK, VITEZSLAV</au><au>LENHART, KAREL</au><au>WELSH, KENNETH I</au><au>DU BOIS, ROLAND M</au><au>PETREK, MARTIN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2002-01-15</date><risdate>2002</risdate><volume>165</volume><issue>2</issue><spage>148</spage><epage>151</epage><pages>148-151</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>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.</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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