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Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA
To study the contribution of the CD14 gene to the pathogenesis of rheumatoid arthritis (RA) in Japanese patients. CD14 genotyping was carried out at the -159C/T dimorphic site in 97 RA patients and 104 normal subjects by the PCR-RFLP (restriction fragment length polymorphism) HLA-DRB1 genotyping was...
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Published in: | Clinical and experimental rheumatology 2008-03, Vol.26 (2), p.337-339 |
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creator | TAKEUCHI, F NAKAUE, N KOBAYASHI, N KUWATA, S MURAYAMA, T KAWASUGI, K MORI, M MATSUTA, K |
description | To study the contribution of the CD14 gene to the pathogenesis of rheumatoid arthritis (RA) in Japanese patients.
CD14 genotyping was carried out at the -159C/T dimorphic site in 97 RA patients and 104 normal subjects by the PCR-RFLP (restriction fragment length polymorphism)
HLA-DRB1 genotyping was performed by the PCR-SSCP (sequence specific conformational polymorphism) method.
The -159C/T dimorphism is not associated with whole RA or with female RA, and the results were compatible with a previous report from Germany. The -159C/T dimorphism was not associated with rheumatoid factor (RF)-positive RA, although the -159T allele tended to be associated with RF in the German report. The -159C/T dimorphism showed no association even in RA patients with the RA-susceptibility HLA-DRB1*0405. The -159T allele was prevalent in Japanese controls.
The CD14 gene is very unlikely to be genetically involved in the pathogenesis of Japanese RA. |
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CD14 genotyping was carried out at the -159C/T dimorphic site in 97 RA patients and 104 normal subjects by the PCR-RFLP (restriction fragment length polymorphism)
HLA-DRB1 genotyping was performed by the PCR-SSCP (sequence specific conformational polymorphism) method.
The -159C/T dimorphism is not associated with whole RA or with female RA, and the results were compatible with a previous report from Germany. The -159C/T dimorphism was not associated with rheumatoid factor (RF)-positive RA, although the -159T allele tended to be associated with RF in the German report. The -159C/T dimorphism showed no association even in RA patients with the RA-susceptibility HLA-DRB1*0405. The -159T allele was prevalent in Japanese controls.
The CD14 gene is very unlikely to be genetically involved in the pathogenesis of Japanese RA.</description><identifier>ISSN: 0392-856X</identifier><identifier>EISSN: 1593-098X</identifier><identifier>PMID: 18565258</identifier><language>eng</language><publisher>Pisa: Clinical and Experimental Rheumatology</publisher><subject>Aged ; Arthritis, Rheumatoid - ethnology ; Arthritis, Rheumatoid - genetics ; Biological and medical sciences ; Diseases of the osteoarticular system ; Female ; Genetic Predisposition to Disease - ethnology ; Genotype ; Humans ; Inflammatory joint diseases ; Japan - epidemiology ; Lipopolysaccharide Receptors - genetics ; Male ; Medical sciences ; Middle Aged ; Polymorphism, Restriction Fragment Length ; Polymorphism, Single-Stranded Conformational ; Prevalence ; Promoter Regions, Genetic - genetics</subject><ispartof>Clinical and experimental rheumatology, 2008-03, Vol.26 (2), p.337-339</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20358158$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18565258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAKEUCHI, F</creatorcontrib><creatorcontrib>NAKAUE, N</creatorcontrib><creatorcontrib>KOBAYASHI, N</creatorcontrib><creatorcontrib>KUWATA, S</creatorcontrib><creatorcontrib>MURAYAMA, T</creatorcontrib><creatorcontrib>KAWASUGI, K</creatorcontrib><creatorcontrib>MORI, M</creatorcontrib><creatorcontrib>MATSUTA, K</creatorcontrib><title>Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA</title><title>Clinical and experimental rheumatology</title><addtitle>Clin Exp Rheumatol</addtitle><description>To study the contribution of the CD14 gene to the pathogenesis of rheumatoid arthritis (RA) in Japanese patients.
CD14 genotyping was carried out at the -159C/T dimorphic site in 97 RA patients and 104 normal subjects by the PCR-RFLP (restriction fragment length polymorphism)
HLA-DRB1 genotyping was performed by the PCR-SSCP (sequence specific conformational polymorphism) method.
The -159C/T dimorphism is not associated with whole RA or with female RA, and the results were compatible with a previous report from Germany. The -159C/T dimorphism was not associated with rheumatoid factor (RF)-positive RA, although the -159T allele tended to be associated with RF in the German report. The -159C/T dimorphism showed no association even in RA patients with the RA-susceptibility HLA-DRB1*0405. The -159T allele was prevalent in Japanese controls.
The CD14 gene is very unlikely to be genetically involved in the pathogenesis of Japanese RA.</description><subject>Aged</subject><subject>Arthritis, Rheumatoid - ethnology</subject><subject>Arthritis, Rheumatoid - genetics</subject><subject>Biological and medical sciences</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Genetic Predisposition to Disease - ethnology</subject><subject>Genotype</subject><subject>Humans</subject><subject>Inflammatory joint diseases</subject><subject>Japan - epidemiology</subject><subject>Lipopolysaccharide Receptors - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Polymorphism, Single-Stranded Conformational</subject><subject>Prevalence</subject><subject>Promoter Regions, Genetic - genetics</subject><issn>0392-856X</issn><issn>1593-098X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo9kE1LxDAQhoMo7rr6FyQXvRXz0WSbo1RdlQVBVlhPJU2nbqRtapIe_PdGXT0NPPPMy8scoDkVimdEFdtDNCdcsawQcjtDJyG8E8KkkMtjNKMJCiaKOXpdwQDRGmzcEL2tp2jdgF2L4w5weUNznKXE8mqDG9s7P-5s6LEdftajd72L4LGHt--rhB_1qAcIgJ-vT9FRq7sAZ_u5QC93t5vyPls_rR7K63U2Mq5ixhjTStSQK2BFnXOhGsKJ0VpJTnNYQssT1A0piDaklpKZnLaMCkO1lIXiC3T5m5vqfEwQYtXbYKDrUhE3hUoqxhTJZRLP9-JU99BUo7e99p_V3zOScLEXdDC6a70ejA3_HiNcFDR5Xw7HZuE</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>TAKEUCHI, F</creator><creator>NAKAUE, N</creator><creator>KOBAYASHI, N</creator><creator>KUWATA, S</creator><creator>MURAYAMA, T</creator><creator>KAWASUGI, K</creator><creator>MORI, M</creator><creator>MATSUTA, K</creator><general>Clinical and Experimental Rheumatology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20080301</creationdate><title>Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA</title><author>TAKEUCHI, F ; NAKAUE, N ; KOBAYASHI, N ; KUWATA, S ; MURAYAMA, T ; KAWASUGI, K ; MORI, M ; MATSUTA, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p239t-222a95be49e28b4359d030caa96314e7ef3435ad080ac0b662c41f215c1a66893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Arthritis, Rheumatoid - ethnology</topic><topic>Arthritis, Rheumatoid - genetics</topic><topic>Biological and medical sciences</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Genetic Predisposition to Disease - ethnology</topic><topic>Genotype</topic><topic>Humans</topic><topic>Inflammatory joint diseases</topic><topic>Japan - epidemiology</topic><topic>Lipopolysaccharide Receptors - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Polymorphism, Single-Stranded Conformational</topic><topic>Prevalence</topic><topic>Promoter Regions, Genetic - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAKEUCHI, F</creatorcontrib><creatorcontrib>NAKAUE, N</creatorcontrib><creatorcontrib>KOBAYASHI, N</creatorcontrib><creatorcontrib>KUWATA, S</creatorcontrib><creatorcontrib>MURAYAMA, T</creatorcontrib><creatorcontrib>KAWASUGI, K</creatorcontrib><creatorcontrib>MORI, M</creatorcontrib><creatorcontrib>MATSUTA, K</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>MEDLINE - Academic</collection><jtitle>Clinical and experimental rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAKEUCHI, F</au><au>NAKAUE, N</au><au>KOBAYASHI, N</au><au>KUWATA, S</au><au>MURAYAMA, T</au><au>KAWASUGI, K</au><au>MORI, M</au><au>MATSUTA, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA</atitle><jtitle>Clinical and experimental rheumatology</jtitle><addtitle>Clin Exp Rheumatol</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>26</volume><issue>2</issue><spage>337</spage><epage>339</epage><pages>337-339</pages><issn>0392-856X</issn><eissn>1593-098X</eissn><abstract>To study the contribution of the CD14 gene to the pathogenesis of rheumatoid arthritis (RA) in Japanese patients.
CD14 genotyping was carried out at the -159C/T dimorphic site in 97 RA patients and 104 normal subjects by the PCR-RFLP (restriction fragment length polymorphism)
HLA-DRB1 genotyping was performed by the PCR-SSCP (sequence specific conformational polymorphism) method.
The -159C/T dimorphism is not associated with whole RA or with female RA, and the results were compatible with a previous report from Germany. The -159C/T dimorphism was not associated with rheumatoid factor (RF)-positive RA, although the -159T allele tended to be associated with RF in the German report. The -159C/T dimorphism showed no association even in RA patients with the RA-susceptibility HLA-DRB1*0405. The -159T allele was prevalent in Japanese controls.
The CD14 gene is very unlikely to be genetically involved in the pathogenesis of Japanese RA.</abstract><cop>Pisa</cop><pub>Clinical and Experimental Rheumatology</pub><pmid>18565258</pmid><tpages>3</tpages></addata></record> |
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subjects | Aged Arthritis, Rheumatoid - ethnology Arthritis, Rheumatoid - genetics Biological and medical sciences Diseases of the osteoarticular system Female Genetic Predisposition to Disease - ethnology Genotype Humans Inflammatory joint diseases Japan - epidemiology Lipopolysaccharide Receptors - genetics Male Medical sciences Middle Aged Polymorphism, Restriction Fragment Length Polymorphism, Single-Stranded Conformational Prevalence Promoter Regions, Genetic - genetics |
title | Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA |
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