Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk:a meta-analysis of ob-servational studies
Objective To clarify the association between rs1050450 polymorphism in Glutathione peroxidase-1 (GPx-1) and the risk of cardi-ovascular diseases (CVD) by performing a meta-analysis of published studies. There is growing evidence from different study types for an association of the GPx-1 polymorphism...
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creator | Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN |
description | Objective To clarify the association between rs1050450 polymorphism in Glutathione peroxidase-1 (GPx-1) and the risk of cardi-ovascular diseases (CVD) by performing a meta-analysis of published studies. There is growing evidence from different study types for an association of the GPx-1 polymorphism and cardiovascular outcomes, but observational studies have so far shown inconsistent results. Me-thods Relevant publications were searched through PubMed, Embase database databases and the Cochrane Library. We used odds ratios (ORs) with 95%confidence intervals (CIs) to assess the strength of association under the best genetic model. Both Q statistic and the I2 were used to check heterogeneity. Meta-regression analysis was performed to explore heterogeneity source. Sensitivity analysis, cumulative me-ta-analysis analysis and publication bias were used to test the reliability of the results. Results Data were available from two cohort studies and 8 case-control studies involving 1,430 cases and 3,767 controls. The pooled ORs for overall CVD risk was 1.36 with 95%CI:1.08-1.70 under a co-dominant model, and that for East Asian subgroup was 1.84 (95%CI:1.39-2.43). Substantial heterogeneity for ORs were de-tected among all the included studies, mainly caused by ethnic differences between East Asian and non-East Asian populations. Although Egger's regression test suggested no statistical significant publication bias, Begg's funnel plot exhibited obvious asymmetry. The statistical significance disappeared after adjusting for potential publication bias in the overall studies. However, no substantial publication bias was found in the East Asian subgroup. Conclusions GPx-1 gene Pro198Leu and Pro197Leu polymorphisms considerably increased the risk of CVD in the East Asian population. Large-scale investigations are needed to confirm the results in different ethnicities. |
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There is growing evidence from different study types for an association of the GPx-1 polymorphism and cardiovascular outcomes, but observational studies have so far shown inconsistent results. Me-thods Relevant publications were searched through PubMed, Embase database databases and the Cochrane Library. We used odds ratios (ORs) with 95%confidence intervals (CIs) to assess the strength of association under the best genetic model. Both Q statistic and the I2 were used to check heterogeneity. Meta-regression analysis was performed to explore heterogeneity source. Sensitivity analysis, cumulative me-ta-analysis analysis and publication bias were used to test the reliability of the results. Results Data were available from two cohort studies and 8 case-control studies involving 1,430 cases and 3,767 controls. The pooled ORs for overall CVD risk was 1.36 with 95%CI:1.08-1.70 under a co-dominant model, and that for East Asian subgroup was 1.84 (95%CI:1.39-2.43). Substantial heterogeneity for ORs were de-tected among all the included studies, mainly caused by ethnic differences between East Asian and non-East Asian populations. Although Egger's regression test suggested no statistical significant publication bias, Begg's funnel plot exhibited obvious asymmetry. The statistical significance disappeared after adjusting for potential publication bias in the overall studies. However, no substantial publication bias was found in the East Asian subgroup. Conclusions GPx-1 gene Pro198Leu and Pro197Leu polymorphisms considerably increased the risk of CVD in the East Asian population. Large-scale investigations are needed to confirm the results in different ethnicities.</description><identifier>ISSN: 1671-5411</identifier><language>eng</language><subject>Meta分析 ; 东亚人群 ; 关联强度 ; 协会 ; 基因多态性 ; 心血管疾病 ; 谷胱甘肽过氧化物酶 ; 风险</subject><ispartof>老年心脏病学杂志:英文版, 2014 (2), p.141-150</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/88644X/88644X.jpg</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids></links><search><creatorcontrib>Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN</creatorcontrib><title>Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk:a meta-analysis of ob-servational studies</title><title>老年心脏病学杂志:英文版</title><addtitle>Journal of Geriatric Cardiology</addtitle><description>Objective To clarify the association between rs1050450 polymorphism in Glutathione peroxidase-1 (GPx-1) and the risk of cardi-ovascular diseases (CVD) by performing a meta-analysis of published studies. There is growing evidence from different study types for an association of the GPx-1 polymorphism and cardiovascular outcomes, but observational studies have so far shown inconsistent results. Me-thods Relevant publications were searched through PubMed, Embase database databases and the Cochrane Library. We used odds ratios (ORs) with 95%confidence intervals (CIs) to assess the strength of association under the best genetic model. Both Q statistic and the I2 were used to check heterogeneity. Meta-regression analysis was performed to explore heterogeneity source. Sensitivity analysis, cumulative me-ta-analysis analysis and publication bias were used to test the reliability of the results. Results Data were available from two cohort studies and 8 case-control studies involving 1,430 cases and 3,767 controls. The pooled ORs for overall CVD risk was 1.36 with 95%CI:1.08-1.70 under a co-dominant model, and that for East Asian subgroup was 1.84 (95%CI:1.39-2.43). Substantial heterogeneity for ORs were de-tected among all the included studies, mainly caused by ethnic differences between East Asian and non-East Asian populations. Although Egger's regression test suggested no statistical significant publication bias, Begg's funnel plot exhibited obvious asymmetry. The statistical significance disappeared after adjusting for potential publication bias in the overall studies. However, no substantial publication bias was found in the East Asian subgroup. Conclusions GPx-1 gene Pro198Leu and Pro197Leu polymorphisms considerably increased the risk of CVD in the East Asian population. Large-scale investigations are needed to confirm the results in different ethnicities.</description><subject>Meta分析</subject><subject>东亚人群</subject><subject>关联强度</subject><subject>协会</subject><subject>基因多态性</subject><subject>心血管疾病</subject><subject>谷胱甘肽过氧化物酶</subject><subject>风险</subject><issn>1671-5411</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNzktOwzAUhWEPQKI89nBZgCW7iWkYIsRjwKAD5tUlcZMLjh18ndLsALbAClhE9pQt0AILYHT0SWfwH4iZvlhoaXKtj8Qx87NSpjD5fCa-rphDSZgoeAhrqF2fMDU7WehsDFuqkK3UMI3vd8ut1NP4AZG1Mio3CpYx6MviwfaAvvrVYq8uuKENsWuIW4Y3Sg2UGCsKG-SydxghEr9M4ydCaxNK9OgGJt4nhCfJNm5-ktABp74iy6ficI2O7dnfnojz25vH63tZNsHXr-TrVRepxTisjMpUpot59p_PN-z6X60</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope></search><sort><creationdate>2014</creationdate><title>Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk:a meta-analysis of ob-servational studies</title><author>Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-chongqing_primary_503031823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Meta分析</topic><topic>东亚人群</topic><topic>关联强度</topic><topic>协会</topic><topic>基因多态性</topic><topic>心血管疾病</topic><topic>谷胱甘肽过氧化物酶</topic><topic>风险</topic><toplevel>online_resources</toplevel><creatorcontrib>Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</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><jtitle>老年心脏病学杂志:英文版</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jun-Xia ZHANG Zhi-Mei WANG Jun-Jie ZHANG Lin-Lin ZHU Xiao-Fei GAO Shao-Liang CHEN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk:a meta-analysis of ob-servational studies</atitle><jtitle>老年心脏病学杂志:英文版</jtitle><addtitle>Journal of Geriatric Cardiology</addtitle><date>2014</date><risdate>2014</risdate><issue>2</issue><spage>141</spage><epage>150</epage><pages>141-150</pages><issn>1671-5411</issn><abstract>Objective To clarify the association between rs1050450 polymorphism in Glutathione peroxidase-1 (GPx-1) and the risk of cardi-ovascular diseases (CVD) by performing a meta-analysis of published studies. There is growing evidence from different study types for an association of the GPx-1 polymorphism and cardiovascular outcomes, but observational studies have so far shown inconsistent results. Me-thods Relevant publications were searched through PubMed, Embase database databases and the Cochrane Library. We used odds ratios (ORs) with 95%confidence intervals (CIs) to assess the strength of association under the best genetic model. Both Q statistic and the I2 were used to check heterogeneity. Meta-regression analysis was performed to explore heterogeneity source. Sensitivity analysis, cumulative me-ta-analysis analysis and publication bias were used to test the reliability of the results. Results Data were available from two cohort studies and 8 case-control studies involving 1,430 cases and 3,767 controls. The pooled ORs for overall CVD risk was 1.36 with 95%CI:1.08-1.70 under a co-dominant model, and that for East Asian subgroup was 1.84 (95%CI:1.39-2.43). Substantial heterogeneity for ORs were de-tected among all the included studies, mainly caused by ethnic differences between East Asian and non-East Asian populations. Although Egger's regression test suggested no statistical significant publication bias, Begg's funnel plot exhibited obvious asymmetry. The statistical significance disappeared after adjusting for potential publication bias in the overall studies. However, no substantial publication bias was found in the East Asian subgroup. Conclusions GPx-1 gene Pro198Leu and Pro197Leu polymorphisms considerably increased the risk of CVD in the East Asian population. Large-scale investigations are needed to confirm the results in different ethnicities.</abstract></addata></record> |
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source | EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Meta分析 东亚人群 关联强度 协会 基因多态性 心血管疾病 谷胱甘肽过氧化物酶 风险 |
title | Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk:a meta-analysis of ob-servational studies |
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