Lipoprotein lipase gene polymorphism and lipid profile in coronary artery disease

gdc.relation.journal Archives of Pathology & Laboratory Medicine en_US
dc.contributor.author Duman, Belgin Süsleyici
dc.contributor.author Türkoğlu, Caner
dc.contributor.author Akpinar, Belhhan
dc.contributor.author Güden, Mustafa
dc.contributor.author Vertii, Alexey
dc.contributor.author Dak, Esranur
dc.contributor.author Çağatay, Tülin
dc.contributor.author Günay, Demet
dc.contributor.author Buyukdevrim, Ahmet Sevim
dc.contributor.other 01. Kadir Has University
dc.date.accessioned 2019-06-27T08:00:54Z
dc.date.available 2019-06-27T08:00:54Z
dc.date.issued 2004
dc.description.abstract Context.-Lipoprotein lipase (LPL) plays a central role in lipid metabolism hydrolyzing triglyceride in chylomicrons and very-low-density lipoproteins. The PvuII polymorphic variant of LPL gene is common and might affect risk of coronary artery disease (CAD). Objective.-Our aim was to determine whether LPL-PvuII polymorphism can be considered to be an independent risk factor or a predictor for CAD in Turkish subjects. Design.-We used polymerase chain reaction and restriction enzyme digestion to determine the distribution of the previously described C-->T transition that causes a PvuII polymorphism in intron 6 among healthy blood donors of Turkish origin and among angiographically confirmed CAD patients with comparable ethnic backgrounds. Results.-For the PvuII genotypes within the CAD group (n = 80) the +/- genotype was found in 39 individuals (48.8%) whereas 25 (31.3%) carried the +/+ genotype and 14 (17.5%) carried the -/- genotype. Within the control group (n = 49) the -/- genotype was found in 19 individuals (38.8%) 16 (32.7%) carried the +/- genotype and 14 (28.6%) carried the +/+ genotype. The genotype frequency distribution was significantly different (P = .049) in the CAD and control study groups. The most frequent genotype among CAD patients was +/- en_US]
dc.description.abstract this genotype was more frequent in patients than in control subjects. However the -/- genotype was more prevalent in the control group. Lipoprotein lipase-PvuII polymorphism was found to be associated with fasting total cholesterol and low-density lipoprotein cholesterol levels. The +/+ genotype was found to have higher levels of total cholesterol and low-density lipoprotein cholesterol in both the CAD and control groups. Conclusion.-There was a difference in the distribution of LPL-PvuII genotypes between the healthy subjects and the patients with CAD. Lipoprotein lipase-PvuII polymorphisms were not detected as independent risk factors for CAD in this study group but had associations with lipid levels. en_US]
dc.identifier.citationcount 9
dc.identifier.issn 0003-9985 en_US
dc.identifier.issn 1543-2165 en_US
dc.identifier.issn 0003-9985
dc.identifier.issn 1543-2165
dc.identifier.scopus 2-s2.0-3543013748 en_US
dc.identifier.uri https://hdl.handle.net/20.500.12469/151
dc.language.iso en en_US
dc.publisher COLL AMER PATHOLOGISTS en_US
dc.relation.ispartof Archives of Pathology & Laboratory Medicine
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Lipoprotein lipase gene polymorphism and lipid profile in coronary artery disease en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.endpage 874
gdc.description.issue 8
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 869 en_US
gdc.description.volume 128 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W1911300180
gdc.identifier.pmid 15270617 en_US
gdc.identifier.wos WOS:000222998800007 en_US
gdc.oaire.accesstype GOLD
gdc.oaire.diamondjournal false
gdc.oaire.impulse 1.0
gdc.oaire.influence 3.2464835E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Male
gdc.oaire.keywords Genotype
gdc.oaire.keywords Turkey
gdc.oaire.keywords Smoking
gdc.oaire.keywords Coronary Disease
gdc.oaire.keywords Comorbidity
gdc.oaire.keywords Middle Aged
gdc.oaire.keywords Introns
gdc.oaire.keywords Lipoproteins, LDL
gdc.oaire.keywords Lipoprotein Lipase
gdc.oaire.keywords Cholesterol
gdc.oaire.keywords Amino Acid Substitution
gdc.oaire.keywords Gene Frequency
gdc.oaire.keywords Risk Factors
gdc.oaire.keywords Humans
gdc.oaire.keywords Female
gdc.oaire.keywords Genetic Predisposition to Disease
gdc.oaire.keywords Deoxyribonucleases, Type II Site-Specific
gdc.oaire.keywords Polymorphism, Restriction Fragment Length
gdc.oaire.popularity 2.4971916E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.fwci 0.195
gdc.openalex.normalizedpercentile 0.82
gdc.opencitations.count 14
gdc.plumx.mendeley 22
gdc.plumx.pubmedcites 7
gdc.plumx.scopuscites 12
gdc.scopus.citedcount 12
gdc.wos.citedcount 9
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relation.isOrgUnitOfPublication.latestForDiscovery b20623fc-1264-4244-9847-a4729ca7508c

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