Association of interleukin-1 receptor antagonist +2018 gene polymorphism with Japanese chronic periodontitis patients using a novel genotyping method

Summary Genetic variants at multiple loci have been shown to be associated with periodontitis risk. In this study, we have focused on nine functional gene polymorphisms encoding immunoregulation‐related molecules such as cytokines (interleukin‐1 (IL‐1), transforming growth factor‐β1 (TGF‐β1)) and ce...

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Veröffentlicht in:International journal of immunogenetics 2008-04, Vol.35 (2), p.165-170
Hauptverfasser: Komatsu, Y., Galicia, J. C., Kobayashi, T., Yamazaki, K., Yoshie, H.
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container_issue 2
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container_title International journal of immunogenetics
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creator Komatsu, Y.
Galicia, J. C.
Kobayashi, T.
Yamazaki, K.
Yoshie, H.
description Summary Genetic variants at multiple loci have been shown to be associated with periodontitis risk. In this study, we have focused on nine functional gene polymorphisms encoding immunoregulation‐related molecules such as cytokines (interleukin‐1 (IL‐1), transforming growth factor‐β1 (TGF‐β1)) and cell surface receptors (immunoglobulin G and A Fc receptors (FcγR and FcαR)). In total, 113 Japanese patients with chronic periodontitis (CP) and 108 race‐matched healthy controls were genotyped with the modified serial invasive signal amplification reaction. There was a significant difference in the distribution of IL‐1 receptor antagonist (RN) +2018 T/C allele between the patient and control groups, with enrichment of the +2018 C in controls (P = 0.021, odds ratio = 0.38). An increased frequency of the IL‐1 haplotype comprising IL‐1A +4845 G, IL‐1B –31 C, and IL‐1RN +2018 C was observed in controls (P = 0.004). Moreover, a multivariate logistic regression analysis revealed that subjects with IL‐1RN +2018 C allele were less likely to have CP (P = 0.016, odds ratio = 0.29). These findings document the association of IL‐1RN +2018 C with reduced susceptibility to CP in the Japanese.
doi_str_mv 10.1111/j.1744-313X.2008.00757.x
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An increased frequency of the IL‐1 haplotype comprising IL‐1A +4845 G, IL‐1B –31 C, and IL‐1RN +2018 C was observed in controls (P = 0.004). Moreover, a multivariate logistic regression analysis revealed that subjects with IL‐1RN +2018 C allele were less likely to have CP (P = 0.016, odds ratio = 0.29). 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C.</creatorcontrib><creatorcontrib>Kobayashi, T.</creatorcontrib><creatorcontrib>Yamazaki, K.</creatorcontrib><creatorcontrib>Yoshie, H.</creatorcontrib><title>Association of interleukin-1 receptor antagonist +2018 gene polymorphism with Japanese chronic periodontitis patients using a novel genotyping method</title><title>International journal of immunogenetics</title><addtitle>Int J Immunogenet</addtitle><description>Summary Genetic variants at multiple loci have been shown to be associated with periodontitis risk. In this study, we have focused on nine functional gene polymorphisms encoding immunoregulation‐related molecules such as cytokines (interleukin‐1 (IL‐1), transforming growth factor‐β1 (TGF‐β1)) and cell surface receptors (immunoglobulin G and A Fc receptors (FcγR and FcαR)). In total, 113 Japanese patients with chronic periodontitis (CP) and 108 race‐matched healthy controls were genotyped with the modified serial invasive signal amplification reaction. There was a significant difference in the distribution of IL‐1 receptor antagonist (RN) +2018 T/C allele between the patient and control groups, with enrichment of the +2018 C in controls (P = 0.021, odds ratio = 0.38). An increased frequency of the IL‐1 haplotype comprising IL‐1A +4845 G, IL‐1B –31 C, and IL‐1RN +2018 C was observed in controls (P = 0.004). Moreover, a multivariate logistic regression analysis revealed that subjects with IL‐1RN +2018 C allele were less likely to have CP (P = 0.016, odds ratio = 0.29). 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C.</creatorcontrib><creatorcontrib>Kobayashi, T.</creatorcontrib><creatorcontrib>Yamazaki, K.</creatorcontrib><creatorcontrib>Yoshie, H.</creatorcontrib><collection>Istex</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>International journal of immunogenetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komatsu, Y.</au><au>Galicia, J. C.</au><au>Kobayashi, T.</au><au>Yamazaki, K.</au><au>Yoshie, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of interleukin-1 receptor antagonist +2018 gene polymorphism with Japanese chronic periodontitis patients using a novel genotyping method</atitle><jtitle>International journal of immunogenetics</jtitle><addtitle>Int J Immunogenet</addtitle><date>2008-04</date><risdate>2008</risdate><volume>35</volume><issue>2</issue><spage>165</spage><epage>170</epage><pages>165-170</pages><issn>1744-3121</issn><eissn>1744-313X</eissn><abstract>Summary Genetic variants at multiple loci have been shown to be associated with periodontitis risk. In this study, we have focused on nine functional gene polymorphisms encoding immunoregulation‐related molecules such as cytokines (interleukin‐1 (IL‐1), transforming growth factor‐β1 (TGF‐β1)) and cell surface receptors (immunoglobulin G and A Fc receptors (FcγR and FcαR)). In total, 113 Japanese patients with chronic periodontitis (CP) and 108 race‐matched healthy controls were genotyped with the modified serial invasive signal amplification reaction. There was a significant difference in the distribution of IL‐1 receptor antagonist (RN) +2018 T/C allele between the patient and control groups, with enrichment of the +2018 C in controls (P = 0.021, odds ratio = 0.38). An increased frequency of the IL‐1 haplotype comprising IL‐1A +4845 G, IL‐1B –31 C, and IL‐1RN +2018 C was observed in controls (P = 0.004). Moreover, a multivariate logistic regression analysis revealed that subjects with IL‐1RN +2018 C allele were less likely to have CP (P = 0.016, odds ratio = 0.29). These findings document the association of IL‐1RN +2018 C with reduced susceptibility to CP in the Japanese.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18321309</pmid><doi>10.1111/j.1744-313X.2008.00757.x</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Alleles
Asian Continental Ancestry Group
Chronic Disease
Female
Genetic Predisposition to Disease - genetics
Haplotypes
Humans
Interleukin 1 Receptor Antagonist Protein - genetics
Japan
Male
Middle Aged
Periodontitis - genetics
Polymorphism, Single Nucleotide
title Association of interleukin-1 receptor antagonist +2018 gene polymorphism with Japanese chronic periodontitis patients using a novel genotyping method
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