Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33050
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dc.contributor.authorErgören, Mahmut Çerkez-
dc.date.accessioned2023-06-15T13:16:06Z-
dc.date.available2023-06-15T13:16:06Z-
dc.date.issued2019-01-
dc.identifier.citationTemel, S. G. ve Ergören, M. C. (2019). ''The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease''. Anatolian Journal of Cardiology, 21(1), 31-38.tr_TR
dc.identifier.issn2149-2263-
dc.identifier.issn2149-2271-
dc.identifier.urihttps://doi.org/10.14744/AnatolJCardiol.2018.90907-
dc.identifier.urihttps://anatoljcardiol.com/jvi.aspx?un=AJC-90907-
dc.identifier.urihttp://hdl.handle.net/11452/33050-
dc.description.abstractObjective: Recent genome-wide association studies have established that polymorphisms within CDKN2B-ASI of chr9p21.3 locus increased susceptibility to coronary artery disease (CAD) or myocardial infarction. Common variants of CDKN2B-AS1 (including rs4977574 A>G and rs1333040 C>T) are determined to be directly associated with CADs in many populations worldwide and suggested biomarkers for the early detection of CAD. There is a lack of investigation for the association between CDKN2B-AS1 rs4977574 A>G and rs1333040 C>T genetic modifiers and CAD in a Turkish Cypriot population. The aim of the present study was to investigate the potential effects of these variants on susceptibility to developing CAD in a Turkish Cypriot population and their contribution to lipid metabolism. Methods: Seventy-one patients with angiography-confirmed CAD were recruited to the CAD group, whereas 153 voluntary subjects without CAD symptoms were enrolled to the control group. Genotyping for the CDKN2B-AS1 gene polymorphisms was performed by polymerase chain reaction, followed by restriction fragment length polymorphism analysis. Results: There is no statistical significant association observed between rs4977574 and rs1333040 single-nucleotide polymorphisms and two studied groups [odds ratio (OR): 0.763, p=0.185, 95% confidence interval (CI): 0.511-1.139 and OR: 1.060, p=0.802, 95% CI: 0.672-1.671, respectively]. However, rs2977574 G and rs1333040 T alleles-the risk alleles-were found to be associated with higher level of serum total cholesterol and lower level of high-density lipoprotein-cholesterol in the CAD group (p=0.019, p=0.006 and p=0.022, p=0.031, respectively). To our knowledge, this is the first study that establishes the effect of rs1333040 on lipid metabolism. Conclusion: The presence of rs4977574 G and rs1333040 T alleles and interaction may exist as environmental factors associated with lipid metabolism and might be responsible for the development of CAD in a Turkish Cypriot population.en_US
dc.language.isoenen_US
dc.publisherAvesen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCardiovascular system & cardiologyen_US
dc.subjectChr9p21en_US
dc.subjectRs4977574en_US
dc.subjectRs1333040en_US
dc.subjectBiomarkersen_US
dc.subjectCoronary artery diseaseen_US
dc.subjectGenome-wide asscociationen_US
dc.subjectMyocardial-infarctionen_US
dc.subjectCardiovascular-diseaseen_US
dc.subjectLocusen_US
dc.subjectPolymorphismsen_US
dc.subjectPopulationen_US
dc.subjectRS4977574en_US
dc.subjectRisken_US
dc.subjectSnpsen_US
dc.subjectAtherosclerosisen_US
dc.subject.meshAdulten_US
dc.subject.meshBiomarkersen_US
dc.subject.meshCoronary angiographyen_US
dc.subject.meshCoronary artery diseaseen_US
dc.subject.meshCyclin-dependent kinase inhibitor p15en_US
dc.subject.meshEuropean continental ancestry groupen_US
dc.subject.meshFemaleen_US
dc.subject.meshGenetic predisposition to diseaseen_US
dc.subject.meshHumansen_US
dc.subject.meshLipid metabolismen_US
dc.subject.meshMaleen_US
dc.subject.meshPolymorphism, single nucleotideen_US
dc.subject.meshTurkeyen_US
dc.titleThe association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery diseaseen_US
dc.typeArticleen_US
dc.identifier.wos000462344800007tr_TR
dc.identifier.scopus2-s2.0-85059242312tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri/Histoloji ve Embriyoloji Bölümü.tr_TR
dc.contributor.orcid0000-0001-9593-9325tr_TR
dc.contributor.orcid0000-0001-9593-9325tr_TR
dc.contributor.orcid0000-0002-9802-0880tr_TR
dc.identifier.startpage31tr_TR
dc.identifier.endpage38tr_TR
dc.identifier.volume21tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalAnatolian Journal of Cardiologyen_US
dc.contributor.buuauthorTemel, Şehime Gülsün-
dc.contributor.researcheridD-8491-2018tr_TR
dc.contributor.researcheridAAZ-6885-2021tr_TR
dc.contributor.researcheridGQP-2509-2022tr_TR
dc.contributor.researcheridAAG-8385-2021tr_TR
dc.indexed.trdizinTrDizintr_TR
dc.identifier.pubmed30587704tr_TR
dc.subject.wosCardiac & cardiovascular systemsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid6507885442tr_TR
dc.contributor.scopusid56731124900tr_TR
dc.subject.scopusCoronary Artery Disease; Sortilin; Genetic Predispositionen_US
dc.subject.emtreeBiological markeren_US
dc.subject.emtreeCyclin dependent kinase inhibitor 2Ben_US
dc.subject.emtreeGenomic DNAen_US
dc.subject.emtreeGlucoseen_US
dc.subject.emtreeHigh density lipoprotein cholesterolen_US
dc.subject.emtreeTriacylglycerolen_US
dc.subject.emtreeBiological markeren_US
dc.subject.emtreeCdkn2b protein, humanen_US
dc.subject.emtreeCyclin dependent kinase inhibitor 2Ben_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCholesterol blood levelen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCoronary artery diseaseen_US
dc.subject.emtreeDNA extractionen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGene frequencyen_US
dc.subject.emtreeGenetic associationen_US
dc.subject.emtreeGenetic susceptibilityen_US
dc.subject.emtreeGenetic variabilityen_US
dc.subject.emtreeGenotypeen_US
dc.subject.emtreeGlucose blood levelen_US
dc.subject.emtreeHaplotypeen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeLipid metabolismen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeRestriction fragment length polymorphismen_US
dc.subject.emtreeRisk factoren_US
dc.subject.emtreeSingle nucleotide polymorphismen_US
dc.subject.emtreeBlooden_US
dc.subject.emtreeCaucasianen_US
dc.subject.emtreeCoronary angiographyen_US
dc.subject.emtreeCoronary artery diseaseen_US
dc.subject.emtreeDiagnostic imagingen_US
dc.subject.emtreeGenetic predispositionen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeTurkey (bird)en_US
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