Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis

The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk. Based on the search of PubMed, Web of Science (IS...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2013-03, Vol.8 (3), p.e60472-e60472
Hauptverfasser: Wang, Meiyun, Jiang, Xiubo, Wu, Wenlong, Zhang, Dongfeng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e60472
container_issue 3
container_start_page e60472
container_title PloS one
container_volume 8
creator Wang, Meiyun
Jiang, Xiubo
Wu, Wenlong
Zhang, Dongfeng
description The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk. Based on the search of PubMed, Web of Science (ISI), CNKI (National Knowledge Infrastructure), Wan Fang Med Online and CBM (Chinese Biology Medical Literature Database) databases, all eligible case-control or cohort studies were identified. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) from fixed and random effect models were calculated. Heterogeneity among studies was evaluated using the I(2). Meta-regression was used to explore the potential sources of between-study heterogeneity. Begg's test was used to estimate publication bias. Our study included 27 articles, contained 28 independent case-control studies, involved a total of 3,742 cases and 3,691 controls about 4b/a, 1,800 cases and 1,751 controls about T-786C and 2,747 cases and 2,872 controls about G894T. A significant association of 4a allele with increased risk of IS was found in dominant (FEM: OR = 1.498, 95% CI = 1.329-1.689), recessive (FEM: OR = 2.132, 95% CI = 1.383-3.286) and codominant (REM: OR = 1.456, 95% CI = 1.235-1.716) models. For T-786C and G894T, there were significant associations with dominant and codominant genetic models, but not with recessive genetic model. The meta-analysis indicated that eNOS gene 4b/a, T-786C, G894T polymorphism might be associated with IS.
doi_str_mv 10.1371/journal.pone.0060472
format Article
fullrecord <record><control><sourceid>proquest_plos_</sourceid><recordid>TN_cdi_plos_journals_1330899988</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_e5a8f597f02d4905a36ff915ddb26867</doaj_id><sourcerecordid>1322732567</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-5f4fbd20653062dea2e72322652fd040f695d26ea4804fc30e4ffcfba9f6b18a3</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCIfsA_QGCJSy-7OP5KwgGpqgpUqugFztYkHm-869jBziLtvyfb3VYt4jTW-L03b0avKN6VdFnyqvy0jtsUwC_HGHBJqaKiYi-K07LhbKEY5S-fvE-Ks5zXlEpeK_W6OGFcClEKflpsroOJU4_egSc_7kjehamHjGSFAckY_W6IaexdHjKBYEhyeUOiJS53PQ6uI3lKcYPEBXKZHYSZMm49TC6GzwTIgBMsYLa5yy6_KV5Z8BnfHut58evr9c-r74vbu283V5e3i04yNS2kFbY1jCrJqWIGgWHFOGNKMmuooFY10jCFIGoqbMcpCms720JjVVvWwM-LDwfd0cesj3fKuuSc1k3T1PWMuDkgTIS1HpMbIO10BKfvGzGtNKTJdR41SqitbCpLmRENlcCVtU0pjWmZqlU1a305Ttu2A5oOw5TAPxN9_hNcr1fxj-aKNpVQs8DFUSDF31vMkx7m66L3EDBu974ZqziT97M-_gP9_3bigOpSzDmhfTRTUr3PzgNL77Ojj9mZae-fLvJIeggL_wv1xcPD</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1330899988</pqid></control><display><type>article</type><title>Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis</title><source>PLoS</source><source>MEDLINE</source><source>Full-Text Journals in Chemistry (Open access)</source><source>DOAJ Directory of Open Access Journals</source><source>PubMed Central</source><source>EZB Electronic Journals Library</source><creator>Wang, Meiyun ; Jiang, Xiubo ; Wu, Wenlong ; Zhang, Dongfeng</creator><creatorcontrib>Wang, Meiyun ; Jiang, Xiubo ; Wu, Wenlong ; Zhang, Dongfeng</creatorcontrib><description>The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk. Based on the search of PubMed, Web of Science (ISI), CNKI (National Knowledge Infrastructure), Wan Fang Med Online and CBM (Chinese Biology Medical Literature Database) databases, all eligible case-control or cohort studies were identified. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) from fixed and random effect models were calculated. Heterogeneity among studies was evaluated using the I(2). Meta-regression was used to explore the potential sources of between-study heterogeneity. Begg's test was used to estimate publication bias. Our study included 27 articles, contained 28 independent case-control studies, involved a total of 3,742 cases and 3,691 controls about 4b/a, 1,800 cases and 1,751 controls about T-786C and 2,747 cases and 2,872 controls about G894T. A significant association of 4a allele with increased risk of IS was found in dominant (FEM: OR = 1.498, 95% CI = 1.329-1.689), recessive (FEM: OR = 2.132, 95% CI = 1.383-3.286) and codominant (REM: OR = 1.456, 95% CI = 1.235-1.716) models. For T-786C and G894T, there were significant associations with dominant and codominant genetic models, but not with recessive genetic model. The meta-analysis indicated that eNOS gene 4b/a, T-786C, G894T polymorphism might be associated with IS.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0060472</identifier><identifier>PMID: 23544143</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Asian Continental Ancestry Group - genetics ; Biology ; Blood pressure ; Brain Ischemia - complications ; Brain Ischemia - genetics ; Case-Control Studies ; Confidence intervals ; Epidemiology ; Gene polymorphism ; Genetic analysis ; Genetic Heterogeneity ; Genetic Predisposition to Disease ; Health risks ; Heterogeneity ; Humans ; Ischemia ; Medical ethics ; Medicine ; Meta-analysis ; Nitric oxide ; Nitric Oxide Synthase Type III - genetics ; Nitric-oxide synthase ; Polymorphism ; Polymorphism, Single Nucleotide - genetics ; Publication Bias ; Regression analysis ; Risk ; Risk Factors ; Rodents ; Statistical analysis ; Stroke ; Stroke - complications ; Stroke - genetics</subject><ispartof>PloS one, 2013-03, Vol.8 (3), p.e60472-e60472</ispartof><rights>2013 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Wang et al 2013 Wang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-5f4fbd20653062dea2e72322652fd040f695d26ea4804fc30e4ffcfba9f6b18a3</citedby><cites>FETCH-LOGICAL-c526t-5f4fbd20653062dea2e72322652fd040f695d26ea4804fc30e4ffcfba9f6b18a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609746/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609746/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23544143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Meiyun</creatorcontrib><creatorcontrib>Jiang, Xiubo</creatorcontrib><creatorcontrib>Wu, Wenlong</creatorcontrib><creatorcontrib>Zhang, Dongfeng</creatorcontrib><title>Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk. Based on the search of PubMed, Web of Science (ISI), CNKI (National Knowledge Infrastructure), Wan Fang Med Online and CBM (Chinese Biology Medical Literature Database) databases, all eligible case-control or cohort studies were identified. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) from fixed and random effect models were calculated. Heterogeneity among studies was evaluated using the I(2). Meta-regression was used to explore the potential sources of between-study heterogeneity. Begg's test was used to estimate publication bias. Our study included 27 articles, contained 28 independent case-control studies, involved a total of 3,742 cases and 3,691 controls about 4b/a, 1,800 cases and 1,751 controls about T-786C and 2,747 cases and 2,872 controls about G894T. A significant association of 4a allele with increased risk of IS was found in dominant (FEM: OR = 1.498, 95% CI = 1.329-1.689), recessive (FEM: OR = 2.132, 95% CI = 1.383-3.286) and codominant (REM: OR = 1.456, 95% CI = 1.235-1.716) models. For T-786C and G894T, there were significant associations with dominant and codominant genetic models, but not with recessive genetic model. The meta-analysis indicated that eNOS gene 4b/a, T-786C, G894T polymorphism might be associated with IS.</description><subject>Asian Continental Ancestry Group - genetics</subject><subject>Biology</subject><subject>Blood pressure</subject><subject>Brain Ischemia - complications</subject><subject>Brain Ischemia - genetics</subject><subject>Case-Control Studies</subject><subject>Confidence intervals</subject><subject>Epidemiology</subject><subject>Gene polymorphism</subject><subject>Genetic analysis</subject><subject>Genetic Heterogeneity</subject><subject>Genetic Predisposition to Disease</subject><subject>Health risks</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Ischemia</subject><subject>Medical ethics</subject><subject>Medicine</subject><subject>Meta-analysis</subject><subject>Nitric oxide</subject><subject>Nitric Oxide Synthase Type III - genetics</subject><subject>Nitric-oxide synthase</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Publication Bias</subject><subject>Regression analysis</subject><subject>Risk</subject><subject>Risk Factors</subject><subject>Rodents</subject><subject>Statistical analysis</subject><subject>Stroke</subject><subject>Stroke - complications</subject><subject>Stroke - genetics</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIfsA_QGCJSy-7OP5KwgGpqgpUqugFztYkHm-869jBziLtvyfb3VYt4jTW-L03b0avKN6VdFnyqvy0jtsUwC_HGHBJqaKiYi-K07LhbKEY5S-fvE-Ks5zXlEpeK_W6OGFcClEKflpsroOJU4_egSc_7kjehamHjGSFAckY_W6IaexdHjKBYEhyeUOiJS53PQ6uI3lKcYPEBXKZHYSZMm49TC6GzwTIgBMsYLa5yy6_KV5Z8BnfHut58evr9c-r74vbu283V5e3i04yNS2kFbY1jCrJqWIGgWHFOGNKMmuooFY10jCFIGoqbMcpCms720JjVVvWwM-LDwfd0cesj3fKuuSc1k3T1PWMuDkgTIS1HpMbIO10BKfvGzGtNKTJdR41SqitbCpLmRENlcCVtU0pjWmZqlU1a305Ttu2A5oOw5TAPxN9_hNcr1fxj-aKNpVQs8DFUSDF31vMkx7m66L3EDBu974ZqziT97M-_gP9_3bigOpSzDmhfTRTUr3PzgNL77Ojj9mZae-fLvJIeggL_wv1xcPD</recordid><startdate>20130327</startdate><enddate>20130327</enddate><creator>Wang, Meiyun</creator><creator>Jiang, Xiubo</creator><creator>Wu, Wenlong</creator><creator>Zhang, Dongfeng</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130327</creationdate><title>Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis</title><author>Wang, Meiyun ; Jiang, Xiubo ; Wu, Wenlong ; Zhang, Dongfeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-5f4fbd20653062dea2e72322652fd040f695d26ea4804fc30e4ffcfba9f6b18a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Asian Continental Ancestry Group - genetics</topic><topic>Biology</topic><topic>Blood pressure</topic><topic>Brain Ischemia - complications</topic><topic>Brain Ischemia - genetics</topic><topic>Case-Control Studies</topic><topic>Confidence intervals</topic><topic>Epidemiology</topic><topic>Gene polymorphism</topic><topic>Genetic analysis</topic><topic>Genetic Heterogeneity</topic><topic>Genetic Predisposition to Disease</topic><topic>Health risks</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Ischemia</topic><topic>Medical ethics</topic><topic>Medicine</topic><topic>Meta-analysis</topic><topic>Nitric oxide</topic><topic>Nitric Oxide Synthase Type III - genetics</topic><topic>Nitric-oxide synthase</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Publication Bias</topic><topic>Regression analysis</topic><topic>Risk</topic><topic>Risk Factors</topic><topic>Rodents</topic><topic>Statistical analysis</topic><topic>Stroke</topic><topic>Stroke - complications</topic><topic>Stroke - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Meiyun</creatorcontrib><creatorcontrib>Jiang, Xiubo</creatorcontrib><creatorcontrib>Wu, Wenlong</creatorcontrib><creatorcontrib>Zhang, Dongfeng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Database‎ (1962 - current)</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>https://resources.nclive.org/materials</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Meiyun</au><au>Jiang, Xiubo</au><au>Wu, Wenlong</au><au>Zhang, Dongfeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-03-27</date><risdate>2013</risdate><volume>8</volume><issue>3</issue><spage>e60472</spage><epage>e60472</epage><pages>e60472-e60472</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk. Based on the search of PubMed, Web of Science (ISI), CNKI (National Knowledge Infrastructure), Wan Fang Med Online and CBM (Chinese Biology Medical Literature Database) databases, all eligible case-control or cohort studies were identified. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) from fixed and random effect models were calculated. Heterogeneity among studies was evaluated using the I(2). Meta-regression was used to explore the potential sources of between-study heterogeneity. Begg's test was used to estimate publication bias. Our study included 27 articles, contained 28 independent case-control studies, involved a total of 3,742 cases and 3,691 controls about 4b/a, 1,800 cases and 1,751 controls about T-786C and 2,747 cases and 2,872 controls about G894T. A significant association of 4a allele with increased risk of IS was found in dominant (FEM: OR = 1.498, 95% CI = 1.329-1.689), recessive (FEM: OR = 2.132, 95% CI = 1.383-3.286) and codominant (REM: OR = 1.456, 95% CI = 1.235-1.716) models. For T-786C and G894T, there were significant associations with dominant and codominant genetic models, but not with recessive genetic model. The meta-analysis indicated that eNOS gene 4b/a, T-786C, G894T polymorphism might be associated with IS.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23544143</pmid><doi>10.1371/journal.pone.0060472</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2013-03, Vol.8 (3), p.e60472-e60472
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1330899988
source PLoS; MEDLINE; Full-Text Journals in Chemistry (Open access); DOAJ Directory of Open Access Journals; PubMed Central; EZB Electronic Journals Library
subjects Asian Continental Ancestry Group - genetics
Biology
Blood pressure
Brain Ischemia - complications
Brain Ischemia - genetics
Case-Control Studies
Confidence intervals
Epidemiology
Gene polymorphism
Genetic analysis
Genetic Heterogeneity
Genetic Predisposition to Disease
Health risks
Heterogeneity
Humans
Ischemia
Medical ethics
Medicine
Meta-analysis
Nitric oxide
Nitric Oxide Synthase Type III - genetics
Nitric-oxide synthase
Polymorphism
Polymorphism, Single Nucleotide - genetics
Publication Bias
Regression analysis
Risk
Risk Factors
Rodents
Statistical analysis
Stroke
Stroke - complications
Stroke - genetics
title Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T16%3A11%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Endothelial%20NO%20synthase%20gene%20polymorphisms%20and%20risk%20of%20ischemic%20stroke%20in%20Asian%20population:%20a%20meta-analysis&rft.jtitle=PloS%20one&rft.au=Wang,%20Meiyun&rft.date=2013-03-27&rft.volume=8&rft.issue=3&rft.spage=e60472&rft.epage=e60472&rft.pages=e60472-e60472&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0060472&rft_dat=%3Cproquest_plos_%3E1322732567%3C/proquest_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1330899988&rft_id=info:pmid/23544143&rft_doaj_id=oai_doaj_org_article_e5a8f597f02d4905a36ff915ddb26867&rfr_iscdi=true