Publication:
The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease

dc.contributor.authorErgören, Mahmut Çerkez
dc.contributor.buuauthorTemel, Şehime Gülsün
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTemel Tıp Bilimleri
dc.contributor.departmentHistoloji ve Embriyoloji Bölümü
dc.contributor.orcid0000-0001-9593-9325
dc.contributor.orcid0000-0001-9593-9325
dc.contributor.orcid0000-0002-9802-0880
dc.contributor.researcheridD-8491-2018
dc.contributor.researcheridAAZ-6885-2021
dc.contributor.researcheridGQP-2509-2022
dc.contributor.researcheridAAG-8385-2021
dc.contributor.scopusid6507885442
dc.contributor.scopusid56731124900
dc.date.accessioned2023-06-15T13:16:06Z
dc.date.available2023-06-15T13:16:06Z
dc.date.issued2019-01
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.
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.
dc.identifier.endpage38
dc.identifier.issn2149-2263
dc.identifier.issn2149-2271
dc.identifier.issue1
dc.identifier.pubmed30587704
dc.identifier.scopus2-s2.0-85059242312
dc.identifier.startpage31
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.identifier.volume21
dc.identifier.wos000462344800007
dc.indexed.scopusScopus
dc.indexed.trdizinTrDizin
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherAves
dc.relation.journalAnatolian Journal of Cardiology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCardiovascular system & cardiology
dc.subjectChr9p21
dc.subjectRs4977574
dc.subjectRs1333040
dc.subjectBiomarkers
dc.subjectCoronary artery disease
dc.subjectGenome-wide asscociation
dc.subjectMyocardial-infarction
dc.subjectCardiovascular-disease
dc.subjectLocus
dc.subjectPolymorphisms
dc.subjectPopulation
dc.subjectRS4977574
dc.subjectRisk
dc.subjectSnps
dc.subjectAtherosclerosis
dc.subject.emtreeBiological marker
dc.subject.emtreeCyclin dependent kinase inhibitor 2B
dc.subject.emtreeGenomic DNA
dc.subject.emtreeGlucose
dc.subject.emtreeHigh density lipoprotein cholesterol
dc.subject.emtreeTriacylglycerol
dc.subject.emtreeBiological marker
dc.subject.emtreeCdkn2b protein, human
dc.subject.emtreeCyclin dependent kinase inhibitor 2B
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeCholesterol blood level
dc.subject.emtreeControlled study
dc.subject.emtreeCoronary artery disease
dc.subject.emtreeDNA extraction
dc.subject.emtreeFemale
dc.subject.emtreeGene frequency
dc.subject.emtreeGenetic association
dc.subject.emtreeGenetic susceptibility
dc.subject.emtreeGenetic variability
dc.subject.emtreeGenotype
dc.subject.emtreeGlucose blood level
dc.subject.emtreeHaplotype
dc.subject.emtreeHuman
dc.subject.emtreeLipid metabolism
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeRestriction fragment length polymorphism
dc.subject.emtreeRisk factor
dc.subject.emtreeSingle nucleotide polymorphism
dc.subject.emtreeBlood
dc.subject.emtreeCaucasian
dc.subject.emtreeCoronary angiography
dc.subject.emtreeCoronary artery disease
dc.subject.emtreeDiagnostic imaging
dc.subject.emtreeGenetic predisposition
dc.subject.emtreeGenetics
dc.subject.emtreeTurkey (bird)
dc.subject.meshAdult
dc.subject.meshBiomarkers
dc.subject.meshCoronary angiography
dc.subject.meshCoronary artery disease
dc.subject.meshCyclin-dependent kinase inhibitor p15
dc.subject.meshEuropean continental ancestry group
dc.subject.meshFemale
dc.subject.meshGenetic predisposition to disease
dc.subject.meshHumans
dc.subject.meshLipid metabolism
dc.subject.meshMale
dc.subject.meshPolymorphism, single nucleotide
dc.subject.meshTurkey
dc.subject.scopusCoronary Artery Disease; Sortilin; Genetic Predisposition
dc.subject.wosCardiac & cardiovascular systems
dc.titleThe association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease
dc.typeArticle
dc.wos.quartileQ4
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Temel Tıp Bilimleri/Histoloji ve Embriyoloji Bölümü
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
Şehime_Ergören_2019.pdf
Size:
124.48 KB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
Placeholder
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: