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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angiology 2009-04, Vol.60 (2), p.180-185
Hauptverfasser: Liu, Wenwei, Tang, Qizhu, Jiang, Hua, Ding, Xiangwu, Liu, Yongsheng, Zhu, Rui, Tang, Yongqian, Li, Bin, Wei, Min
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 185
container_issue 2
container_start_page 180
container_title Angiology
container_volume 60
creator Liu, Wenwei
Tang, Qizhu
Jiang, Hua
Ding, Xiangwu
Liu, Yongsheng
Zhu, Rui
Tang, Yongqian
Li, Bin
Wei, Min
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.
doi_str_mv 10.1177/0003319708319939
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_746230821</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_0003319708319939</sage_id><sourcerecordid>746230821</sourcerecordid><originalsourceid>FETCH-LOGICAL-c397t-ac1cff344134845b0ecbfcfbd66e90cabc2f99e576b3b6886d9b9213d3edd0cb3</originalsourceid><addsrcrecordid>eNp9kM1PwyAYh4nRuFm9ezJc1FMVCv3guMyvJUvcQS9eGqAwO1uYsJr0v5e5RhMTPQB5eZ_fS3gAOMXoCuM8v0YIEYJZjoqwM8L2wBgzimKc5nQfjLfteNsfgSPvV6FMMcoOwQgXKWOUkTF4WTjb2o1ycGGbvrVu_Vr7FloNZybcNqp7q02MC1gbODHL2i4dD4jkTdPDkP1QBk6ts4a7Hk5ciPTwpvaKe3UMDjRvvDoZzgg8390-TR_i-eP9bDqZx5KwfBNziaXWhFJMaEFTgZQUWmpRZZliSHIhE82YSvNMEJEVRVYxwRJMKqKqCklBInC5m7t29r1TflO2tZeqabhRtvNlTrOEoCJEInDxL5nlmDD0BaIdKJ313ildrl3dhi-WGJVb8-Vv8yFyNszuRKuqn8CgOgDnA8B90KcdN7L231yCaUrSsCIQ7zjPl6pc2c6ZYO_vhz8BSV6ZCg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67139021</pqid></control><display><type>article</type><title>Promoter Polymorphism of Interleukin-18 in Angiographically Proven Coronary Artery Disease</title><source>MEDLINE</source><source>SAGE Complete</source><creator>Liu, Wenwei ; Tang, Qizhu ; Jiang, Hua ; Ding, Xiangwu ; Liu, Yongsheng ; Zhu, Rui ; Tang, Yongqian ; Li, Bin ; Wei, Min</creator><creatorcontrib>Liu, Wenwei ; Tang, Qizhu ; Jiang, Hua ; Ding, Xiangwu ; Liu, Yongsheng ; Zhu, Rui ; Tang, Yongqian ; Li, Bin ; Wei, Min</creatorcontrib><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 &lt; 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P &lt; 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&amp;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 &lt; 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P &lt; 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 &lt; 0.001; control patients: 65.9±31.6 vs 42.4±19.5 pg/ml, P &lt; 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>
fulltext fulltext
identifier ISSN: 0003-3197
ispartof Angiology, 2009-04, Vol.60 (2), p.180-185
issn 0003-3197
1940-1574
language eng
recordid cdi_proquest_miscellaneous_746230821
source MEDLINE; SAGE Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T04%3A56%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Promoter%20Polymorphism%20of%20Interleukin-18%20in%20Angiographically%20Proven%20Coronary%20Artery%20Disease&rft.jtitle=Angiology&rft.au=Liu,%20Wenwei&rft.date=2009-04-01&rft.volume=60&rft.issue=2&rft.spage=180&rft.epage=185&rft.pages=180-185&rft.issn=0003-3197&rft.eissn=1940-1574&rft.coden=ANGIAB&rft_id=info:doi/10.1177/0003319708319939&rft_dat=%3Cproquest_cross%3E746230821%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67139021&rft_id=info:pmid/18599493&rft_sage_id=10.1177_0003319708319939&rfr_iscdi=true