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Variation in the vascular endothelial growth factor gene, carotid intima-media thickness and the risk of acute myocardial infarction.

Identifieur interne : 000412 ( PubMed/Corpus ); précédent : 000411; suivant : 000413

Variation in the vascular endothelial growth factor gene, carotid intima-media thickness and the risk of acute myocardial infarction.

Auteurs : Tiia Kangas-Kontio ; Jari M. Tapanainen ; Heikki Huikuri ; Eeva-Riitta Savolainen ; Markku P Iv Nsalo ; Heikki Kauma ; Y Antero Kes Niemi ; Markku J. Savolainen ; Sakari Kakko

Source :

RBID : pubmed:19089753

English descriptors

Abstract

Vascular endothelial growth factor (VEGF) is a potent angiogenic growth factor, but its role in atherogenesis is still unclear. Our goal was to study whether three variants of the VEGF gene, previously associated with VEGF production, are linked to atherosclerosis defined as carotid intima-media thickness (IMT) and as the risk of acute myocardial infarction (AMI).

DOI: 10.1080/00365510802607520
PubMed: 19089753

Links to Exploration step

pubmed:19089753

Le document en format XML

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<name sortKey="Kangas Kontio, Tiia" sort="Kangas Kontio, Tiia" uniqKey="Kangas Kontio T" first="Tiia" last="Kangas-Kontio">Tiia Kangas-Kontio</name>
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<nlm:affiliation>Institute of Clinical Medicine, Department of Internal Medicine, Oulu University Hospital and Biocenter Oulu, Finland.</nlm:affiliation>
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<name sortKey="Tapanainen, Jari M" sort="Tapanainen, Jari M" uniqKey="Tapanainen J" first="Jari M" last="Tapanainen">Jari M. Tapanainen</name>
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<name sortKey="Huikuri, Heikki" sort="Huikuri, Heikki" uniqKey="Huikuri H" first="Heikki" last="Huikuri">Heikki Huikuri</name>
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<name sortKey="Savolainen, Eeva Riitta" sort="Savolainen, Eeva Riitta" uniqKey="Savolainen E" first="Eeva-Riitta" last="Savolainen">Eeva-Riitta Savolainen</name>
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<name sortKey="P Iv Nsalo, Markku" sort="P Iv Nsalo, Markku" uniqKey="P Iv Nsalo M" first="Markku" last="P Iv Nsalo">Markku P Iv Nsalo</name>
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<name sortKey="Kauma, Heikki" sort="Kauma, Heikki" uniqKey="Kauma H" first="Heikki" last="Kauma">Heikki Kauma</name>
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<name sortKey="Kes Niemi, Y Antero" sort="Kes Niemi, Y Antero" uniqKey="Kes Niemi Y" first="Y Antero" last="Kes Niemi">Y Antero Kes Niemi</name>
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<title xml:lang="en">Variation in the vascular endothelial growth factor gene, carotid intima-media thickness and the risk of acute myocardial infarction.</title>
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<term>Adult</term>
<term>Atherosclerosis (genetics)</term>
<term>Atherosclerosis (pathology)</term>
<term>Carotid Arteries (ultrasonography)</term>
<term>Cohort Studies</term>
<term>Coronary Artery Disease (genetics)</term>
<term>Coronary Artery Disease (pathology)</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Myocardial Infarction (genetics)</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Risk Factors</term>
<term>Tunica Intima (ultrasonography)</term>
<term>Tunica Media (ultrasonography)</term>
<term>Vascular Endothelial Growth Factor A (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Vascular Endothelial Growth Factor A</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Atherosclerosis</term>
<term>Coronary Artery Disease</term>
<term>Myocardial Infarction</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Atherosclerosis</term>
<term>Coronary Artery Disease</term>
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<keywords scheme="MESH" qualifier="ultrasonography" xml:lang="en">
<term>Carotid Arteries</term>
<term>Tunica Intima</term>
<term>Tunica Media</term>
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<term>Adult</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Risk Factors</term>
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<front>
<div type="abstract" xml:lang="en">Vascular endothelial growth factor (VEGF) is a potent angiogenic growth factor, but its role in atherogenesis is still unclear. Our goal was to study whether three variants of the VEGF gene, previously associated with VEGF production, are linked to atherosclerosis defined as carotid intima-media thickness (IMT) and as the risk of acute myocardial infarction (AMI).</div>
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<Month>03</Month>
<Day>30</Day>
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<DateCompleted>
<Year>2009</Year>
<Month>07</Month>
<Day>07</Day>
</DateCompleted>
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<ISSN IssnType="Electronic">1502-7686</ISSN>
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<Volume>69</Volume>
<Issue>3</Issue>
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<Year>2009</Year>
</PubDate>
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<Title>Scandinavian journal of clinical and laboratory investigation</Title>
<ISOAbbreviation>Scand. J. Clin. Lab. Invest.</ISOAbbreviation>
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<ArticleTitle>Variation in the vascular endothelial growth factor gene, carotid intima-media thickness and the risk of acute myocardial infarction.</ArticleTitle>
<Pagination>
<MedlinePgn>335-43</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1080/00365510802607520</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Vascular endothelial growth factor (VEGF) is a potent angiogenic growth factor, but its role in atherogenesis is still unclear. Our goal was to study whether three variants of the VEGF gene, previously associated with VEGF production, are linked to atherosclerosis defined as carotid intima-media thickness (IMT) and as the risk of acute myocardial infarction (AMI).</AbstractText>
<AbstractText Label="MATERIAL AND METHODS" NlmCategory="METHODS">Three VEGF gene single nucleotide polymorphisms (SNPs) (-2578A>C rs699947, -634C>G rs2010963 and +936C>T rs3025039) were genotyped in 516 control subjects of the OPERA (Oulu Project Elucidating Risk of Atherosclerosis) cohort and in 251 survivors of AMI. In the OPERA cohort, the genotyped SNPs were analysed for their association with IMT. The SNPs were also analysed for their association with the risk of AMI, a complication of advanced atherosclerosis. In addition, haplotype frequencies and their associated effects on IMT and on the risk of AMI were estimated.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">None of the single genotyped polymorphisms was significantly associated with overall IMT or with the risk of AMI. However, the haplotype CCC was associated with higher overall IMT without plaques in women (p = 0.01, haplotypic effect +0.03 mm), the haplotype CCT with higher IMT without plaques in the internal carotid artery in men (p = 0.001, +0.11), while the haplotype AGT was associated with reduced AMI risk (p = 0.015, OR = 0.46).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Variation in the VEGF gene is weakly associated with IMT and the risk of AMI, but the effect can only be observed when the information of the SNPs is combined by constructing haplotypes.</AbstractText>
</Abstract>
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<LastName>Kangas-Kontio</LastName>
<ForeName>Tiia</ForeName>
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<Affiliation>Institute of Clinical Medicine, Department of Internal Medicine, Oulu University Hospital and Biocenter Oulu, Finland.</Affiliation>
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