Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease
Interleukin 18 (IL–18) is a pro-atherogenic cytokine associated with the occurrence of various cardiac complications. The IL–18 gene has a functional −137 G/C polymorphism (rs187238) in the promoter region. Using the ligase detection reaction-polymerase chain reaction, we genotyped a cohort of patie...
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Veröffentlicht in: | Angiology 2009-04, Vol.60 (2), p.180-185 |
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description | Interleukin 18 (IL–18) is a pro-atherogenic cytokine associated with the occurrence of various cardiac complications. The IL–18 gene has a functional −137 G/C polymorphism (rs187238) in the promoter region. Using the ligase detection reaction-polymerase chain reaction, we genotyped a cohort of patients in Chinese Han population in Xiangfan region. Case patients of coronary artery disease and control patients were identified by coronary angiography. The plasma IL–18 concentrations were measured by ELISA. A significant increase of G allele or GG-genotype was observed in 241 case patients compared to 145 control individuals (frequency of G allele = 0.90 vs 0.83, p=0.004; frequency of GG-genotype = 0.81 vs 0.68, p = 0.005). In case patients, G allele carriers in multi-vessel disease patients had a higher occurrence rate when compared to single-vessel disease patients, but no significant difference was detected (frequency of G allele = 0.92 vs 0.88, p=0.107; frequency of GG-genotype = 0.84 vs 0.75, p = 0.089). IL–18 protein concentration of the −137GG genotype was much higher than concentration of the CG and CC genotype (case patients: 229.1±131.5 vs 122.7±73.6 pg/ml, P < 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P < 0.001). To conclude, IL–18 promoter −137G/C polymorphism influences IL–18 levels and the occurrence of coronary artery disease, suggesting that IL–18 is causally involved in the development of atherosclerosis. |
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The IL–18 gene has a functional −137 G/C polymorphism (rs187238) in the promoter region. Using the ligase detection reaction-polymerase chain reaction, we genotyped a cohort of patients in Chinese Han population in Xiangfan region. Case patients of coronary artery disease and control patients were identified by coronary angiography. The plasma IL–18 concentrations were measured by ELISA. A significant increase of G allele or GG-genotype was observed in 241 case patients compared to 145 control individuals (frequency of G allele = 0.90 vs 0.83, p=0.004; frequency of GG-genotype = 0.81 vs 0.68, p = 0.005). In case patients, G allele carriers in multi-vessel disease patients had a higher occurrence rate when compared to single-vessel disease patients, but no significant difference was detected (frequency of G allele = 0.92 vs 0.88, p=0.107; frequency of GG-genotype = 0.84 vs 0.75, p = 0.089). IL–18 protein concentration of the −137GG genotype was much higher than concentration of the CG and CC genotype (case patients: 229.1±131.5 vs 122.7±73.6 pg/ml, P < 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P < 0.001). To conclude, IL–18 promoter −137G/C polymorphism influences IL–18 levels and the occurrence of coronary artery disease, suggesting that IL–18 is causally involved in the development of atherosclerosis.</description><identifier>ISSN: 0003-3197</identifier><identifier>EISSN: 1940-1574</identifier><identifier>DOI: 10.1177/0003319708319939</identifier><identifier>PMID: 18599493</identifier><identifier>CODEN: ANGIAB</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Alleles ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Coronary Angiography - methods ; Coronary Artery Disease - blood ; Coronary Artery Disease - diagnostic imaging ; Coronary Artery Disease - genetics ; Coronary heart disease ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; DNA - genetics ; Enzyme-Linked Immunosorbent Assay ; Female ; Follow-Up Studies ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Heart ; Humans ; Interleukin-18 - blood ; Interleukin-18 - genetics ; Male ; Medical sciences ; Middle Aged ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Prognosis ; Promoter Regions, Genetic ; Retrospective Studies</subject><ispartof>Angiology, 2009-04, Vol.60 (2), p.180-185</ispartof><rights>2009 SAGE Publications</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-ac1cff344134845b0ecbfcfbd66e90cabc2f99e576b3b6886d9b9213d3edd0cb3</citedby><cites>FETCH-LOGICAL-c397t-ac1cff344134845b0ecbfcfbd66e90cabc2f99e576b3b6886d9b9213d3edd0cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0003319708319939$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0003319708319939$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21453545$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18599493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Wenwei</creatorcontrib><creatorcontrib>Tang, Qizhu</creatorcontrib><creatorcontrib>Jiang, Hua</creatorcontrib><creatorcontrib>Ding, Xiangwu</creatorcontrib><creatorcontrib>Liu, Yongsheng</creatorcontrib><creatorcontrib>Zhu, Rui</creatorcontrib><creatorcontrib>Tang, Yongqian</creatorcontrib><creatorcontrib>Li, Bin</creatorcontrib><creatorcontrib>Wei, Min</creatorcontrib><title>Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease</title><title>Angiology</title><addtitle>Angiology</addtitle><description>Interleukin 18 (IL–18) is a pro-atherogenic cytokine associated with the occurrence of various cardiac complications. The IL–18 gene has a functional −137 G/C polymorphism (rs187238) in the promoter region. Using the ligase detection reaction-polymerase chain reaction, we genotyped a cohort of patients in Chinese Han population in Xiangfan region. Case patients of coronary artery disease and control patients were identified by coronary angiography. The plasma IL–18 concentrations were measured by ELISA. A significant increase of G allele or GG-genotype was observed in 241 case patients compared to 145 control individuals (frequency of G allele = 0.90 vs 0.83, p=0.004; frequency of GG-genotype = 0.81 vs 0.68, p = 0.005). In case patients, G allele carriers in multi-vessel disease patients had a higher occurrence rate when compared to single-vessel disease patients, but no significant difference was detected (frequency of G allele = 0.92 vs 0.88, p=0.107; frequency of GG-genotype = 0.84 vs 0.75, p = 0.089). IL–18 protein concentration of the −137GG genotype was much higher than concentration of the CG and CC genotype (case patients: 229.1±131.5 vs 122.7±73.6 pg/ml, P < 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P < 0.001). To conclude, IL–18 promoter −137G/C polymorphism influences IL–18 levels and the occurrence of coronary artery disease, suggesting that IL–18 is causally involved in the development of atherosclerosis.</description><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Coronary Angiography - methods</subject><subject>Coronary Artery Disease - blood</subject><subject>Coronary Artery Disease - diagnostic imaging</subject><subject>Coronary Artery Disease - genetics</subject><subject>Coronary heart disease</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>DNA - genetics</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gene Frequency</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Heart</subject><subject>Humans</subject><subject>Interleukin-18 - blood</subject><subject>Interleukin-18 - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Genetic</subject><subject>Prognosis</subject><subject>Promoter Regions, Genetic</subject><subject>Retrospective Studies</subject><issn>0003-3197</issn><issn>1940-1574</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1PwyAYh4nRuFm9ezJc1FMVCv3guMyvJUvcQS9eGqAwO1uYsJr0v5e5RhMTPQB5eZ_fS3gAOMXoCuM8v0YIEYJZjoqwM8L2wBgzimKc5nQfjLfteNsfgSPvV6FMMcoOwQgXKWOUkTF4WTjb2o1ycGGbvrVu_Vr7FloNZybcNqp7q02MC1gbODHL2i4dD4jkTdPDkP1QBk6ts4a7Hk5ciPTwpvaKe3UMDjRvvDoZzgg8390-TR_i-eP9bDqZx5KwfBNziaXWhFJMaEFTgZQUWmpRZZliSHIhE82YSvNMEJEVRVYxwRJMKqKqCklBInC5m7t29r1TflO2tZeqabhRtvNlTrOEoCJEInDxL5nlmDD0BaIdKJ313ildrl3dhi-WGJVb8-Vv8yFyNszuRKuqn8CgOgDnA8B90KcdN7L231yCaUrSsCIQ7zjPl6pc2c6ZYO_vhz8BSV6ZCg</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Liu, Wenwei</creator><creator>Tang, Qizhu</creator><creator>Jiang, Hua</creator><creator>Ding, Xiangwu</creator><creator>Liu, Yongsheng</creator><creator>Zhu, Rui</creator><creator>Tang, Yongqian</creator><creator>Li, Bin</creator><creator>Wei, Min</creator><general>SAGE Publications</general><general>Sage Publications</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><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20090401</creationdate><title>Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease</title><author>Liu, Wenwei ; Tang, Qizhu ; Jiang, Hua ; Ding, Xiangwu ; Liu, Yongsheng ; Zhu, Rui ; Tang, Yongqian ; Li, Bin ; Wei, Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-ac1cff344134845b0ecbfcfbd66e90cabc2f99e576b3b6886d9b9213d3edd0cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Alleles</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Coronary Angiography - methods</topic><topic>Coronary Artery Disease - blood</topic><topic>Coronary Artery Disease - diagnostic imaging</topic><topic>Coronary Artery Disease - genetics</topic><topic>Coronary heart disease</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>DNA - genetics</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gene Frequency</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Heart</topic><topic>Humans</topic><topic>Interleukin-18 - blood</topic><topic>Interleukin-18 - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Genetic</topic><topic>Prognosis</topic><topic>Promoter Regions, Genetic</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Wenwei</creatorcontrib><creatorcontrib>Tang, Qizhu</creatorcontrib><creatorcontrib>Jiang, Hua</creatorcontrib><creatorcontrib>Ding, Xiangwu</creatorcontrib><creatorcontrib>Liu, Yongsheng</creatorcontrib><creatorcontrib>Zhu, Rui</creatorcontrib><creatorcontrib>Tang, Yongqian</creatorcontrib><creatorcontrib>Li, Bin</creatorcontrib><creatorcontrib>Wei, Min</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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Angiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Wenwei</au><au>Tang, Qizhu</au><au>Jiang, Hua</au><au>Ding, Xiangwu</au><au>Liu, Yongsheng</au><au>Zhu, Rui</au><au>Tang, Yongqian</au><au>Li, Bin</au><au>Wei, Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease</atitle><jtitle>Angiology</jtitle><addtitle>Angiology</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>60</volume><issue>2</issue><spage>180</spage><epage>185</epage><pages>180-185</pages><issn>0003-3197</issn><eissn>1940-1574</eissn><coden>ANGIAB</coden><abstract>Interleukin 18 (IL–18) is a pro-atherogenic cytokine associated with the occurrence of various cardiac complications. The IL–18 gene has a functional −137 G/C polymorphism (rs187238) in the promoter region. Using the ligase detection reaction-polymerase chain reaction, we genotyped a cohort of patients in Chinese Han population in Xiangfan region. Case patients of coronary artery disease and control patients were identified by coronary angiography. The plasma IL–18 concentrations were measured by ELISA. A significant increase of G allele or GG-genotype was observed in 241 case patients compared to 145 control individuals (frequency of G allele = 0.90 vs 0.83, p=0.004; frequency of GG-genotype = 0.81 vs 0.68, p = 0.005). In case patients, G allele carriers in multi-vessel disease patients had a higher occurrence rate when compared to single-vessel disease patients, but no significant difference was detected (frequency of G allele = 0.92 vs 0.88, p=0.107; frequency of GG-genotype = 0.84 vs 0.75, p = 0.089). IL–18 protein concentration of the −137GG genotype was much higher than concentration of the CG and CC genotype (case patients: 229.1±131.5 vs 122.7±73.6 pg/ml, P < 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P < 0.001). To conclude, IL–18 promoter −137G/C polymorphism influences IL–18 levels and the occurrence of coronary artery disease, suggesting that IL–18 is causally involved in the development of atherosclerosis.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>18599493</pmid><doi>10.1177/0003319708319939</doi><tpages>6</tpages></addata></record> |
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subjects | Alleles Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Coronary Angiography - methods Coronary Artery Disease - blood Coronary Artery Disease - diagnostic imaging Coronary Artery Disease - genetics Coronary heart disease Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous DNA - genetics Enzyme-Linked Immunosorbent Assay Female Follow-Up Studies Gene Frequency Genetic Predisposition to Disease Genotype Heart Humans Interleukin-18 - blood Interleukin-18 - genetics Male Medical sciences Middle Aged Polymerase Chain Reaction Polymorphism, Genetic Prognosis Promoter Regions, Genetic Retrospective Studies |
title | Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease |
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