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Association of Gghrelin Polymorphisms with Metabolic Syndrome in Han Nationality Chinese
Objective To investigate the association of ghrelin gene polymorphisms with metabolic syndrome in Han Nationality Chinese. Methods A total of 240 patients with metabolic syndrome and 427 adults aged above forty years were recruited. Genotypes were determined by polymerase chain reaction and restrict...
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Published in: | Biomedical and environmental sciences 2008-06, Vol.21 (3), p.188-192 |
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description | Objective To investigate the association of ghrelin gene polymorphisms with metabolic syndrome in Han Nationality Chinese. Methods A total of 240 patients with metabolic syndrome and 427 adults aged above forty years were recruited. Genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism analysis. Results The allelic frequency of the Leu72Met polymorphism was 17.3% in the patient group and 11.9% in the control group (x^2=7.36, P=0.007). Metabolic syndrome was more prevalent among carriers of the Met72 variant (43.8 vs 33.1%, age- and sex-adjusted odds ratio=1.57, P=0.01). No Arg51Gln variants were found in our study subjects. Conclusion Rather than being associated with its individual components, Leu72Met polymorphism is associated with metabolic syndrome in the Han Nationality Chinese. Arg51Gln polymorphism is rare in the Han Nationality Chinese. |
doi_str_mv | 10.1016/S0895-3988(08)60027-6 |
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Methods A total of 240 patients with metabolic syndrome and 427 adults aged above forty years were recruited. Genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism analysis. Results The allelic frequency of the Leu72Met polymorphism was 17.3% in the patient group and 11.9% in the control group (x^2=7.36, P=0.007). Metabolic syndrome was more prevalent among carriers of the Met72 variant (43.8 vs 33.1%, age- and sex-adjusted odds ratio=1.57, P=0.01). No Arg51Gln variants were found in our study subjects. Conclusion Rather than being associated with its individual components, Leu72Met polymorphism is associated with metabolic syndrome in the Han Nationality Chinese. Arg51Gln polymorphism is rare in the Han Nationality Chinese.</description><identifier>ISSN: 0895-3988</identifier><identifier>EISSN: 2214-0190</identifier><identifier>DOI: 10.1016/S0895-3988(08)60027-6</identifier><language>eng</language><publisher>Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China%National Laboratory of Medical Molecular Biology,School of Basic Medicine, Peking Union Medical College, Institute of Basic Medical Science,Chinese Academy of Medical Science, Beijing 100005, China</publisher><subject>临床分析 ; 代谢综合征 ; 多形态 ; 治疗方法</subject><ispartof>Biomedical and environmental sciences, 2008-06, Vol.21 (3), p.188-192</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-e701d2223a710f0bce4d11c73a48810399536c0d4c53a58e650bafa0f45944d13</citedby><cites>FETCH-LOGICAL-c356t-e701d2223a710f0bce4d11c73a48810399536c0d4c53a58e650bafa0f45944d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84046X/84046X.jpg</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>XU, Ling-Ling</creatorcontrib><creatorcontrib>XIANG, Hong-Ding</creatorcontrib><creatorcontrib>QIU, Chang-Chun</creatorcontrib><creatorcontrib>XU, Qun</creatorcontrib><title>Association of Gghrelin Polymorphisms with Metabolic Syndrome in Han Nationality Chinese</title><title>Biomedical and environmental sciences</title><addtitle>Biomedical and Environmental Sciences</addtitle><description>Objective To investigate the association of ghrelin gene polymorphisms with metabolic syndrome in Han Nationality Chinese. Methods A total of 240 patients with metabolic syndrome and 427 adults aged above forty years were recruited. Genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism analysis. Results The allelic frequency of the Leu72Met polymorphism was 17.3% in the patient group and 11.9% in the control group (x^2=7.36, P=0.007). Metabolic syndrome was more prevalent among carriers of the Met72 variant (43.8 vs 33.1%, age- and sex-adjusted odds ratio=1.57, P=0.01). No Arg51Gln variants were found in our study subjects. Conclusion Rather than being associated with its individual components, Leu72Met polymorphism is associated with metabolic syndrome in the Han Nationality Chinese. Arg51Gln polymorphism is rare in the Han Nationality Chinese.</description><subject>临床分析</subject><subject>代谢综合征</subject><subject>多形态</subject><subject>治疗方法</subject><issn>0895-3988</issn><issn>2214-0190</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo9kE1Lw0AQQBdRsFZ_grCIBz1EZ7-SzbEUbYX6AVXwtmw2m2Zrkq3ZSMm_N63F01zemxkeQpcE7giQ-H4JMhURS6W8AXkbA9Akio_QiFLCIyApHKPRP3KKzkJYA3CScjlCn5MQvHG6c77BvsCzVdnayjX4zVd97dtN6UId8NZ1JX62nc585Qxe9k3e-triAZzrBr_sfV25rsfT0jU22HN0Uugq2IvDHKOPx4f36TxavM6eppNFZJiIu8gmQHJKKdMJgQIyY3lOiEmY5lISYGkqWGwg50YwLaSNBWS60FBwkfIBZWN0_bd3q5tCNyu19j_t8EpQmQ0UQAIbggyY-MNM60NobaE2rat12ysCaldR7SuqXSIFUu0rqnjwrg5e6ZvVtxsOZNp8Fa6yiiaCcskp-wUgZHB0</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>XU, Ling-Ling</creator><creator>XIANG, Hong-Ding</creator><creator>QIU, Chang-Chun</creator><creator>XU, Qun</creator><general>Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China%National Laboratory of Medical Molecular Biology,School of Basic Medicine, Peking Union Medical College, Institute of Basic Medical Science,Chinese Academy of Medical Science, Beijing 100005, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20080601</creationdate><title>Association of Gghrelin Polymorphisms with Metabolic Syndrome in Han Nationality Chinese</title><author>XU, Ling-Ling ; XIANG, Hong-Ding ; QIU, Chang-Chun ; XU, Qun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-e701d2223a710f0bce4d11c73a48810399536c0d4c53a58e650bafa0f45944d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>临床分析</topic><topic>代谢综合征</topic><topic>多形态</topic><topic>治疗方法</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>XU, Ling-Ling</creatorcontrib><creatorcontrib>XIANG, Hong-Ding</creatorcontrib><creatorcontrib>QIU, Chang-Chun</creatorcontrib><creatorcontrib>XU, Qun</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Biomedical and environmental sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>XU, Ling-Ling</au><au>XIANG, Hong-Ding</au><au>QIU, Chang-Chun</au><au>XU, Qun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of Gghrelin Polymorphisms with Metabolic Syndrome in Han Nationality Chinese</atitle><jtitle>Biomedical and environmental sciences</jtitle><addtitle>Biomedical and Environmental Sciences</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>21</volume><issue>3</issue><spage>188</spage><epage>192</epage><pages>188-192</pages><issn>0895-3988</issn><eissn>2214-0190</eissn><abstract>Objective To investigate the association of ghrelin gene polymorphisms with metabolic syndrome in Han Nationality Chinese. Methods A total of 240 patients with metabolic syndrome and 427 adults aged above forty years were recruited. Genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism analysis. Results The allelic frequency of the Leu72Met polymorphism was 17.3% in the patient group and 11.9% in the control group (x^2=7.36, P=0.007). Metabolic syndrome was more prevalent among carriers of the Met72 variant (43.8 vs 33.1%, age- and sex-adjusted odds ratio=1.57, P=0.01). No Arg51Gln variants were found in our study subjects. Conclusion Rather than being associated with its individual components, Leu72Met polymorphism is associated with metabolic syndrome in the Han Nationality Chinese. Arg51Gln polymorphism is rare in the Han Nationality Chinese.</abstract><pub>Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China%National Laboratory of Medical Molecular Biology,School of Basic Medicine, Peking Union Medical College, Institute of Basic Medical Science,Chinese Academy of Medical Science, Beijing 100005, China</pub><doi>10.1016/S0895-3988(08)60027-6</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 临床分析 代谢综合征 多形态 治疗方法 |
title | Association of Gghrelin Polymorphisms with Metabolic Syndrome in Han Nationality Chinese |
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